NP-MRD: Showing NP-Card for 7-Dehydrocholesterol (NP0000147)

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Record Information

Version

1.0

Created at

2005-11-16 15:48:42 UTC

Updated at

2024-04-19 10:00:12 UTC

NP-MRD ID

NP0000147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-Dehydrocholesterol

Description

7-Dehydrocholesterol (7-DHC), also known as provitamin D3 or 5,7-cholestadien-3-b-ol, belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Thus, 7-dehydrocholesterol is also classified as a sterol. 7-Dehydrocholesterol is known as a zoosterol, meaning that it is a sterol isolated from animals (to distinguish those sterols isolated from plants which are called phytosterols). 7-DHC functions in the serum as a cholesterol precursor and is photochemically converted to vitamin D3 in the skin. Therefore 7-DHC functions as provitamin-D3. The presence of 7-DHC in human skin enables humans and other mammals to manufacture vitamin D3 (cholecalciferol) from ultraviolet rays in the sun light, via an intermediate isomer pre-vitamin D3. 7-DHC absorbs UV light most effectively at wavelengths between 290 and 320 nm and, thus, the production of vitamin D3 will occur primarily at those wavelengths (PMID: 9625080 ). The two most important factors that govern the generation of pre-vitamin D3 are the quantity (intensity) and quality (appropriate wavelength) of the UVB irradiation reaching the 7-dehydrocholesterol deep in the stratum basale and stratum spinosum (PMID: 9625080 ). 7-DHC is also found in the milk of several mammalian species, including cows (PMID: 10999630 ; PMID: 225459 ). It was discovered by Nobel-laureate organic chemist Adolf Windaus. 7-DHC can be produced by animals and plants via different pathways (PMID: 23717318 ). It is not produced by fungi in significant amounts. 7-DHC is made by some algae and can also be produced by some bacteria.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

      
  Mrv1652308122017252D          

 31 34  0  0  0  0            999 V2000
 9999.976110001.2192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8390 9999.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.6978 9997.9037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5515 9998.7390    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9761 9998.7390    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1260 9999.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.4115 9999.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 9999.264410000.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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10000.7634 9999.3106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.2483 9999.9779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.763410000.6455    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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10003.624210000.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.049910001.8810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.479210001.0560    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
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 14 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19  5  1  6  0  0  0
 18  1  1  1  0  0  0
M  END

HMDB0000032
     RDKit          3D
7-Dehydrocholesterol
 72 75  0  0  0  0  0  0  0  0999 V2000
    8.0566    0.9921    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7528    0.2078   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0057   -1.2075    0.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7199    0.9012    0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3782    0.2190    0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8188    0.1822   -0.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4745   -0.5072   -0.7156 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6370   -1.9004   -0.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4942    0.3253    0.0444 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.0213    2.1667   -0.5997 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2223   -1.6728   -0.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6969   -0.1372    0.7396 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.3956   -1.1413    0.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758   -0.1057   -0.0877 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.1311   -0.5482   -1.7688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178   -2.5730   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6075   -2.0215    0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6498   -2.2596   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7150    0.4785    1.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0224    3.2234   -0.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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M  END

      
  Mrv1652308122017252D          

 31 34  0  0  0  0            999 V2000
 9999.976110001.2192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8390 9999.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 9999.264410000.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.549910000.3906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0000147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]1(CC[C@@]2([H])C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3/t19-,21+,23-,24+,25+,26+,27-/m1/s1

> <INCHI_KEY>
UCTLRSWJYQTBFZ-DDPQNLDTSA-N

> <FORMULA>
C27H44O

> <MOLECULAR_WEIGHT>
384.6377

> <EXACT_MASS>
384.33921603

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
50.01447282690572

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-7,9-dien-5-ol

> <ALOGPS_LOGP>
7.30

> <JCHEM_LOGP>
6.707309549333335

> <ALOGPS_LOGS>
-6.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.270805421445605

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3681497086596925

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
121.46649999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.48e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-7,9-dien-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0000032
     RDKit          3D
7-Dehydrocholesterol
 72 75  0  0  0  0  0  0  0  0999 V2000
    8.0566    0.9921    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7528    0.2078   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0057   -1.2075    0.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7199    0.9012    0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3782    0.2190    0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8188    0.1822   -0.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4745   -0.5072   -0.7156 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6370   -1.9004   -0.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4942    0.3253    0.0444 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4526    1.6941   -0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0213    2.1667   -0.5997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6243    1.2048    0.3264 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0837    1.0171    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7341    1.9005   -0.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1763    1.7339   -0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7802    0.6804   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2607    0.5501   -0.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9295    0.4877    0.8095 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.2934    0.2119    0.5576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3548   -0.7134    1.5337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8933   -0.6019    1.7586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1116   -0.3737    0.4537 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2223   -1.6728   -0.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6969   -0.1372    0.7396 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8747   -1.4090    0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956   -1.1413    0.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758   -0.1057   -0.0877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3229   -0.4285   -1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8553    0.5602   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3777    0.9798    1.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9301    2.0444   -0.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4724    0.1574   -1.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8796   -1.5942   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1675   -1.8854    0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2900   -1.2633    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0628    0.8462    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6009    1.9604    0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    0.8466    1.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4611   -0.7542    1.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4926   -0.2462   -1.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6278    1.2443   -0.9848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -0.5482   -1.7688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178   -2.5730   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6075   -2.0215    0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6498   -2.2596   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7150    0.4785    1.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1540    2.3975   -0.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7274    1.5666   -1.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0224    3.2234   -0.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4636    2.1017   -1.6106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4124    1.4521    1.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2967    2.7985   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7582    2.4675   -1.3663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4991   -0.3767   -1.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6427    1.3992   -1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8324    1.3957    1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3200   -0.5866   -0.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5933   -1.6441    0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8721   -0.7878    2.5160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030    0.2034    2.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5382   -1.5546    2.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7018   -1.5006   -1.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7789   -2.5029    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2989   -1.9291   -0.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6387    0.0056    1.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042   -2.1198    1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9264   -1.8463   -0.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040   -2.1144    0.7994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2713   -0.7848    1.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4200   -0.2289   -1.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1767    0.2137   -2.2461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1341   -1.4968   -1.7440 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27  9  1  0
 27 12  1  0
 24 13  1  0
 22 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  6
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  1
 14 52  1  0
 15 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  1
 19 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  1
 25 66  1  0
 25 67  1  0
 26 68  1  0
 26 69  1  0
 28 70  1  0
 28 71  1  0
 28 72  1  0
M  END

HEADER    PROTEIN                                 12-AUG-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-AUG-20         0                                  
HETATM    1  C   UNK     0    8666.6228668.943   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8662.6338666.617   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0    8658.6368662.754   0.000  0.00  0.00           O+0
HETATM    4  H   UNK     0    8663.9638664.313   0.000  0.00  0.00           H+0
HETATM    5  H   UNK     0    8666.6228664.313   0.000  0.00  0.00           H+0
HETATM    6  C   UNK     0    8661.3028665.841   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8659.9688665.071   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8659.9688663.531   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8661.3028662.761   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8662.6308665.071   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8662.6308663.531   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8663.9638662.761   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8665.2978663.531   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8665.2948668.166   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8663.9608667.396   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8663.9608665.856   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8665.2948665.086   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8666.6278667.396   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8666.6278665.856   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8668.0928665.380   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8668.9978666.625   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8668.0928667.872   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8668.0928669.412   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8669.4288670.178   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8670.7608669.412   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8672.0968670.178   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8673.4328669.412   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8674.7648670.178   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8673.4328667.872   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8666.7608670.178   0.000  0.00  0.00           C+0
HETATM   31  H   UNK     0    8669.4288668.638   0.000  0.00  0.00           H+0
CONECT    1   18                                                            
CONECT    2   10                                                            
CONECT    3    8                                                            
CONECT    4   16                                                            
CONECT    5   19                                                            
CONECT    6    7   10                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9    3                                                  
CONECT    9    8   11                                                       
CONECT   10   11    6    2   16                                             
CONECT   11   10   12    9                                                  
CONECT   12   11   13                                                       
CONECT   13   12   17                                                       
CONECT   14   15   18                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   10    4                                             
CONECT   17   16   13   19                                                  
CONECT   18   19   22   14    1                                             
CONECT   19   18   20   17    5                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   23   31   18   21                                             
CONECT   23   22   24   30                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   23                                                            
CONECT   31   22                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0000032
HETATM    1  C1  UNL     1       8.057   0.992   0.083  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.753   0.208  -0.069  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.006  -1.207   0.402  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.720   0.901   0.789  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.378   0.219   0.726  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.819   0.182  -0.667  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.475  -0.507  -0.716  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.637  -1.900  -0.231  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.494   0.325   0.044  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.453   1.694  -0.652  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.021   2.167  -0.600  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.624   1.205   0.326  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.084   1.017   0.119  1.00  0.00           C  
HETATM   14  C14 UNL     1      -2.734   1.900  -0.568  1.00  0.00           C  
HETATM   15  C15 UNL     1      -4.176   1.734  -0.791  1.00  0.00           C  
HETATM   16  C16 UNL     1      -4.780   0.680  -0.289  1.00  0.00           C  
HETATM   17  C17 UNL     1      -6.261   0.550  -0.541  1.00  0.00           C  
HETATM   18  C18 UNL     1      -6.929   0.488   0.810  1.00  0.00           C  
HETATM   19  O1  UNL     1      -8.293   0.212   0.558  1.00  0.00           O  
HETATM   20  C19 UNL     1      -6.355  -0.713   1.534  1.00  0.00           C  
HETATM   21  C20 UNL     1      -4.893  -0.602   1.759  1.00  0.00           C  
HETATM   22  C21 UNL     1      -4.112  -0.374   0.454  1.00  0.00           C  
HETATM   23  C22 UNL     1      -4.222  -1.673  -0.382  1.00  0.00           C  
HETATM   24  C23 UNL     1      -2.697  -0.137   0.740  1.00  0.00           C  
HETATM   25  C24 UNL     1      -1.875  -1.409   0.558  1.00  0.00           C  
HETATM   26  C25 UNL     1      -0.396  -1.141   0.865  1.00  0.00           C  
HETATM   27  C26 UNL     1       0.076  -0.106  -0.088  1.00  0.00           C  
HETATM   28  C27 UNL     1      -0.323  -0.429  -1.508  1.00  0.00           C  
HETATM   29  H1  UNL     1       8.855   0.560  -0.566  1.00  0.00           H  
HETATM   30  H2  UNL     1       8.378   0.980   1.144  1.00  0.00           H  
HETATM   31  H3  UNL     1       7.930   2.044  -0.242  1.00  0.00           H  
HETATM   32  H4  UNL     1       6.472   0.157  -1.133  1.00  0.00           H  
HETATM   33  H5  UNL     1       7.880  -1.594  -0.192  1.00  0.00           H  
HETATM   34  H6  UNL     1       6.168  -1.885   0.154  1.00  0.00           H  
HETATM   35  H7  UNL     1       7.290  -1.263   1.468  1.00  0.00           H  
HETATM   36  H8  UNL     1       6.063   0.846   1.842  1.00  0.00           H  
HETATM   37  H9  UNL     1       5.601   1.960   0.528  1.00  0.00           H  
HETATM   38  H10 UNL     1       3.695   0.847   1.360  1.00  0.00           H  
HETATM   39  H11 UNL     1       4.461  -0.754   1.205  1.00  0.00           H  
HETATM   40  H12 UNL     1       4.493  -0.246  -1.407  1.00  0.00           H  
HETATM   41  H13 UNL     1       3.628   1.244  -0.985  1.00  0.00           H  
HETATM   42  H14 UNL     1       2.131  -0.548  -1.769  1.00  0.00           H  
HETATM   43  H15 UNL     1       1.918  -2.573  -0.758  1.00  0.00           H  
HETATM   44  H16 UNL     1       2.608  -2.021   0.865  1.00  0.00           H  
HETATM   45  H17 UNL     1       3.650  -2.260  -0.548  1.00  0.00           H  
HETATM   46  H18 UNL     1       1.715   0.478   1.098  1.00  0.00           H  
HETATM   47  H19 UNL     1       2.154   2.397  -0.165  1.00  0.00           H  
HETATM   48  H20 UNL     1       1.727   1.567  -1.718  1.00  0.00           H  
HETATM   49  H21 UNL     1      -0.022   3.223  -0.262  1.00  0.00           H  
HETATM   50  H22 UNL     1      -0.464   2.102  -1.611  1.00  0.00           H  
HETATM   51  H23 UNL     1      -0.412   1.452   1.367  1.00  0.00           H  
HETATM   52  H24 UNL     1      -2.297   2.798  -1.019  1.00  0.00           H  
HETATM   53  H25 UNL     1      -4.758   2.468  -1.366  1.00  0.00           H  
HETATM   54  H26 UNL     1      -6.499  -0.377  -1.086  1.00  0.00           H  
HETATM   55  H27 UNL     1      -6.643   1.399  -1.154  1.00  0.00           H  
HETATM   56  H28 UNL     1      -6.832   1.396   1.406  1.00  0.00           H  
HETATM   57  H29 UNL     1      -8.320  -0.587  -0.038  1.00  0.00           H  
HETATM   58  H30 UNL     1      -6.593  -1.644   0.995  1.00  0.00           H  
HETATM   59  H31 UNL     1      -6.872  -0.788   2.516  1.00  0.00           H  
HETATM   60  H32 UNL     1      -4.603   0.203   2.442  1.00  0.00           H  
HETATM   61  H33 UNL     1      -4.538  -1.555   2.209  1.00  0.00           H  
HETATM   62  H34 UNL     1      -3.702  -1.501  -1.323  1.00  0.00           H  
HETATM   63  H35 UNL     1      -3.779  -2.503   0.157  1.00  0.00           H  
HETATM   64  H36 UNL     1      -5.299  -1.929  -0.542  1.00  0.00           H  
HETATM   65  H37 UNL     1      -2.639   0.006   1.898  1.00  0.00           H  
HETATM   66  H38 UNL     1      -2.204  -2.120   1.333  1.00  0.00           H  
HETATM   67  H39 UNL     1      -1.926  -1.846  -0.429  1.00  0.00           H  
HETATM   68  H40 UNL     1       0.104  -2.114   0.799  1.00  0.00           H  
HETATM   69  H41 UNL     1      -0.271  -0.785   1.909  1.00  0.00           H  
HETATM   70  H42 UNL     1      -1.420  -0.229  -1.596  1.00  0.00           H  
HETATM   71  H43 UNL     1       0.177   0.214  -2.246  1.00  0.00           H  
HETATM   72  H44 UNL     1      -0.134  -1.497  -1.744  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    4   32
CONECT    3   33   34   35
CONECT    4    5   36   37
CONECT    5    6   38   39
CONECT    6    7   40   41
CONECT    7    8    9   42
CONECT    8   43   44   45
CONECT    9   10   27   46
CONECT   10   11   47   48
CONECT   11   12   49   50
CONECT   12   13   27   51
CONECT   13   14   14   24
CONECT   14   15   52
CONECT   15   16   16   53
CONECT   16   17   22
CONECT   17   18   54   55
CONECT   18   19   20   56
CONECT   19   57
CONECT   20   21   58   59
CONECT   21   22   60   61
CONECT   22   23   24
CONECT   23   62   63   64
CONECT   24   25   65
CONECT   25   26   66   67
CONECT   26   27   68   69
CONECT   27   28
CONECT   28   70   71   72
END

HMDB0000032
     RDKit          3D
7-Dehydrocholesterol
 72 75  0  0  0  0  0  0  0  0999 V2000
    8.0566    0.9921    0.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7528    0.2078   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0057   -1.2075    0.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7199    0.9012    0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3782    0.2190    0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8188    0.1822   -0.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4745   -0.5072   -0.7156 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6370   -1.9004   -0.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4942    0.3253    0.0444 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4526    1.6941   -0.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0213    2.1667   -0.5997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6243    1.2048    0.3264 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0837    1.0171    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7341    1.9005   -0.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1763    1.7339   -0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7802    0.6804   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2607    0.5501   -0.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9295    0.4877    0.8095 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.2934    0.2119    0.5576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3548   -0.7134    1.5337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8933   -0.6019    1.7586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1116   -0.3737    0.4537 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2223   -1.6728   -0.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6969   -0.1372    0.7396 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8747   -1.4090    0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956   -1.1413    0.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758   -0.1057   -0.0877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3229   -0.4285   -1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8553    0.5602   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3777    0.9798    1.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9301    2.0444   -0.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4724    0.1574   -1.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8796   -1.5942   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1675   -1.8854    0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2900   -1.2633    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0628    0.8462    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6009    1.9604    0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    0.8466    1.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4611   -0.7542    1.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4926   -0.2462   -1.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6278    1.2443   -0.9848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1311   -0.5482   -1.7688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178   -2.5730   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6075   -2.0215    0.8654 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6498   -2.2596   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7150    0.4785    1.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1540    2.3975   -0.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7274    1.5666   -1.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0224    3.2234   -0.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4636    2.1017   -1.6106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4124    1.4521    1.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2967    2.7985   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7582    2.4675   -1.3663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4991   -0.3767   -1.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6427    1.3992   -1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8324    1.3957    1.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3200   -0.5866   -0.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5933   -1.6441    0.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8721   -0.7878    2.5160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030    0.2034    2.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5382   -1.5546    2.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7018   -1.5006   -1.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7789   -2.5029    0.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2989   -1.9291   -0.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6387    0.0056    1.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042   -2.1198    1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9264   -1.8463   -0.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040   -2.1144    0.7994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2713   -0.7848    1.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4200   -0.2289   -1.5955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1767    0.2137   -2.2461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1341   -1.4968   -1.7440 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27  9  1  0
 27 12  1  0
 24 13  1  0
 22 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  6
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  1
 14 52  1  0
 15 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  1
 19 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  1
 25 66  1  0
 25 67  1  0
 26 68  1  0
 26 69  1  0
 28 70  1  0
 28 71  1  0
 28 72  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(3beta)-Cholesta-5,7-dien-3-ol	ChEBI
5,7-Cholestadien-3-beta-ol	ChEBI
5,7-Cholestadien-3beta-ol	ChEBI
Provitamin D3	ChEBI
Cholesta-5,7-dien-3beta-ol	Kegg
(3b)-Cholesta-5,7-dien-3-ol	Generator
(3Β)-cholesta-5,7-dien-3-ol	Generator
5,7-Cholestadien-3-b-ol	Generator
5,7-Cholestadien-3-β-ol	Generator
5,7-Cholestadien-3b-ol	Generator
5,7-Cholestadien-3β-ol	Generator
Cholesta-5,7-dien-3b-ol	Generator
Cholesta-5,7-dien-3β-ol	Generator
(-)-7-Dehydrocholesterol	HMDB
10,13-Dimethyl-17-(6-methylheptan-2-yl)-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	HMDB
17-(1,5-Dimethylhexyl)-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	HMDB
5,7-Cholestandien-3-ol	HMDB
5,7-Cholestandien-3beta-ol	HMDB
7,8-Dehydro-cholesterol	HMDB
7,8-Didehydrocholesterol	HMDB
7-Dehydro-cholesterol	HMDB
7-Dehydrocholesterin	HMDB
7DHC	HMDB
Cholesta-5,7-dien-3 beta -ol	HMDB
Cholesta-5,7-dien-3-beta-ol	HMDB
Cholesta-5,7-dien-3-ol	HMDB
Dehydrocholesterin	HMDB
Dehydrocholesterol	HMDB
Delta5,7-Cholestadien-3beta-ol	HMDB
Delta5,7-Cholesterol	HMDB
Delta7-Cholesterol	HMDB
Provitamin-D3	HMDB
Provitamin D(3)	HMDB
Cholesta-5,7-dien-3 beta-ol	HMDB
7-Dehydrocholesterol, (3beta,10alpha)-isomer	HMDB
7-Dehydrocholesterol, (3beta,9beta,10alpha)-isomer	HMDB
7-DHC	HMDB
7-Dehydrocholesterol, (3alpha)-isomer	HMDB
7-Dehydrocholesterol, (3beta,9beta)-isomer	HMDB

Chemical Formula

C₂₇H₄₄O

Average Mass

384.6377 Da

Monoisotopic Mass

384.33922 Da

IUPAC Name

(1S,2R,5S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-7,9-dien-5-ol

Traditional Name

(1S,2R,5S,11R,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-7,9-dien-5-ol

CAS Registry Number

434-16-2

SMILES

[H][C@@]1(CC[C@@]2([H])C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C

InChI Identifier

InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9-10,18-19,21,23-25,28H,6-8,11-17H2,1-5H3/t19-,21+,23-,24+,25+,26+,27-/m1/s1

InChI Key

UCTLRSWJYQTBFZ-DDPQNLDTSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	bgnzk@missouri.edu	MU Metabolomics Center, University of Missouri, Columbia. MO, USA	Dr. Bharat Goel	2023-11-10	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	bgnzk@missouri.edu	MU Metabolomics Center, University of Missouri, Columbia. MO, USA	Dr. Bharat Goel	2023-11-10	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	bgnzk@missouri.edu	MU Metabolomics Center, University of Missouri, Columbia. MO, USA	Dr. Bharat Goel	2023-11-10	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	bgnzk@missouri.edu	MU Metabolomics Center, University of Missouri, Columbia. MO, USA	Dr. Bharat Goel	2023-11-10	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 201 MHz, CDCl3, experimental)	bgnzk@missouri.edu	MU Metabolomics Center, University of Missouri, Columbia. MO, USA	Dr. Bharat Goel	2023-11-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201.216488466 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600.133705802 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, CDCl₃, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Abelmoschus esculentus	FooDB	FooDB
Actinidia chinensis	FooDB	FooDB
Agaricus bisporus	FooDB	FooDB
Agave	FooDB	FooDB
Allium ampeloprasum	FooDB	FooDB
Allium ascalonicum	FooDB	FooDB
Allium cepa	FooDB	FooDB
Allium cepa L.	FooDB	FooDB
Allium fistulosum	FooDB	FooDB
Allium sativum	FooDB	FooDB
Allium schoenoprasum	FooDB	FooDB
Allium tuberosum	FooDB	FooDB
Aloysia triphylla	FooDB	FooDB
Amaranthus	FooDB	FooDB
Amelanchier alnifolia	FooDB	FooDB
Anacardium occidentale	FooDB	FooDB
Ananas comosus	FooDB	FooDB
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anethum graveolens	FooDB	FooDB
Angelica keiskei	FooDB	FooDB
Annona cherimola	FooDB	FooDB
Annona muricata	FooDB	FooDB
Annona reticulata	FooDB	FooDB
Annona squamosa	FooDB	FooDB
Anser anser	FooDB	FooDB
Anthriscus cerefolium	FooDB	FooDB
Apium graveolens	FooDB	FooDB
Apium graveolens var. dulce	FooDB	FooDB
Apium graveolens var. rapaceum	FooDB	FooDB
Apium graveolens var. secalinum	FooDB	FooDB
Arachis hypogaea	FooDB	FooDB
Arctium lappa	FooDB	FooDB
Armoracia rusticana	FooDB	FooDB
Artemisia dracunculus	FooDB	FooDB
Artemisia vulgaris	FooDB	FooDB
Artocarpus altilis	FooDB	FooDB
Artocarpus heterophyllus	FooDB	FooDB
Asparagus officinalis	FooDB	FooDB
Attalea speciosa	FooDB	FooDB
Auricularia auricula-judae	FooDB	FooDB
Auricularia polytricha	FooDB	FooDB
Avena sativa L.	FooDB	FooDB
Averrhoa carambola	FooDB	FooDB
Axinella cannabina	LOTUS Database	35616633
Basella alba	FooDB	FooDB
Benincasa hispida	FooDB	FooDB
Bertholletia excelsa	FooDB	FooDB
Beta vulgaris	FooDB	FooDB
Beta vulgaris ssp. cicla	FooDB	FooDB
Bison bison	FooDB	FooDB
Bombyx mori	LOTUS Database	35616633
Borago officinalis	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Brassica alboglabra	FooDB	FooDB
Brassica juncea	FooDB	FooDB
Brassica napus	FooDB	FooDB
Brassica napus var. napus	FooDB	FooDB
Brassica oleracea	FooDB	FooDB
Brassica oleracea var. botrytis	FooDB	FooDB
Brassica oleracea var. capitata	FooDB	FooDB
Brassica oleracea var. gemmifera	FooDB	FooDB
Brassica oleracea var. gongylodes	FooDB	FooDB
Brassica oleracea var. italica	FooDB	FooDB
Brassica oleracea var. sabauda	FooDB	FooDB
Brassica oleracea var. viridis	FooDB	FooDB
Brassica rapa	FooDB	FooDB
Brassica rapa ssp. chinensis	FooDB	FooDB
Brassica rapa var. pekinensis	FooDB	FooDB
Brassica rapa var. rapa	FooDB	FooDB
Brassica ruvo	FooDB	FooDB
Brosimum alicastrum	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Byrsonima crassifolia	FooDB	FooDB
Cajanus cajan	FooDB	FooDB
Canarium ovatum	FooDB	FooDB
Cannabis sativa	CannabisDB	Not Available
Cantharellus cibarius	FooDB	FooDB
Capparis spinosa	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Capsicum annuum	FooDB	FooDB
Capsicum annuum L.	FooDB	FooDB
Capsicum annuum var. annuum	FooDB	FooDB
Capsicum chinense	FooDB	FooDB
Capsicum pubescens	FooDB	FooDB
Carica papaya L.	FooDB	FooDB
Carissa macrocarpa	FooDB	FooDB
Carthamus tinctorius	FooDB	FooDB
Carum carvi	FooDB	FooDB
Carya	FooDB	FooDB
Carya illinoinensis	FooDB	FooDB
Castanea	FooDB	FooDB
Castanea crenata	FooDB	FooDB
Castanea mollissima	FooDB	FooDB
Castanea sativa	FooDB	FooDB
Ceratonia siliqua	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Chamaemelum nobile	FooDB	FooDB
Chamerion angustifolium	FooDB	FooDB
Chenopodium album	FooDB	FooDB
Chenopodium quinoa	FooDB	FooDB
Chrysanthemum coronarium	FooDB	FooDB
Cicer arietinum	FooDB	FooDB
Cichorium endivia	FooDB	FooDB
Cichorium intybus	FooDB	FooDB
Cinnamomum	FooDB	FooDB
Cinnamomum aromaticum	FooDB	FooDB
Cinnamomum verum	FooDB	FooDB
Cirsium	FooDB	FooDB
Citrullus lanatus	FooDB	FooDB
Citrus ×limon (L.) Burm. f. (pro sp.)	FooDB	FooDB
Citrus aurantiifolia	FooDB	FooDB
Citrus latifolia	FooDB	FooDB
Citrus limon	FooDB	FooDB
Citrus maxima	FooDB	FooDB
Citrus paradisi	FooDB	FooDB
Citrus reticulata	FooDB	FooDB
Citrus X sinensis (L.) Osbeck (pro. sp.)	FooDB	FooDB
Cocos nucifera	FooDB	FooDB
Coffea arabica L.	FooDB	FooDB
Coffea canephora	FooDB	FooDB
Colocasia esculenta	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Corchorus olitorius	FooDB	FooDB
Coriandrum sativum L.	FooDB	FooDB
Corylus	FooDB	FooDB
Corylus avellana	FooDB	FooDB
Crateva religiosa	FooDB	FooDB
Crocus sativus	FooDB	FooDB
Cucumis melo	FooDB	FooDB
Cucumis metuliferus	FooDB	FooDB
Cucumis sativus L.	FooDB	FooDB
Cucurbita	FooDB	FooDB
Cucurbita maxima	FooDB	FooDB
Cucurbita moschata	FooDB	FooDB
Cuminum cyminum	FooDB	FooDB
Curcuma longa	FooDB	FooDB
Cydonia oblonga	FooDB	FooDB
Cymbopogon citratus	FooDB	FooDB
Cynara cardunculus	FooDB	FooDB
Cynara scolymus	FooDB	FooDB
Daucus carota	FooDB	FooDB
Daucus carota ssp. sativus	FooDB	FooDB
Dimocarpus longan	FooDB	FooDB
Dioscorea	FooDB	FooDB
Dioscorea pentaphylla	FooDB	FooDB
Diospyros	FooDB	FooDB
Diospyros kaki	FooDB	FooDB
Diospyros virginiana	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Durio zibethinus	FooDB	FooDB
Dysphania ambrosioides	FooDB	FooDB
Elaeis	FooDB	FooDB
Eleocharis dulcis	FooDB	FooDB
Elettaria cardamomum	FooDB	FooDB
Empetrum nigrum	FooDB	FooDB
Equus caballus	FooDB	FooDB
Eragrostis tef	FooDB	FooDB
Eriobotrya japonica	FooDB	FooDB
Eruca vesicaria subsp. Sativa	FooDB	FooDB
Eugenia javanica	FooDB	FooDB
Eugenia uniflora	FooDB	FooDB
Eutrema japonicum	FooDB	FooDB
Fagopyrum esculentum	FooDB	FooDB
Fagopyrum tataricum	FooDB	FooDB
Fagus	FooDB	FooDB
Feijoa sellowiana	FooDB	FooDB
Festuca argentina	LOTUS Database	35616633
Festuca hieronymi	LOTUS Database	35616633
Ficus carica	FooDB	FooDB
Flammulina velutipes	FooDB	FooDB
Foeniculum vulgare	FooDB	FooDB
Fragaria x ananassa	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Garcinia mangostana	FooDB	FooDB
Gaylussacia baccata	FooDB	FooDB
Ginkgo biloba	FooDB	FooDB
Glycine max	FooDB	FooDB
Gossypium	FooDB	FooDB
Grifola frondosa	FooDB	FooDB
Hedysarum alpinum	FooDB	FooDB
Helianthus annuus L.	FooDB	FooDB
Helianthus tuberosus	FooDB	FooDB
Hibiscus sabbariffa	FooDB	FooDB
Hippophae rhamnoides	FooDB	FooDB
Hordeum vulgare	FooDB	FooDB
Hyssopus officinalis L.	FooDB	FooDB
Illicium verum	FooDB	FooDB
Ipomoea aquatica	FooDB	FooDB
Ipomoea batatas	FooDB	FooDB
Juglans	FooDB	FooDB
Juglans ailanthifolia	FooDB	FooDB
Juglans cinerea	FooDB	FooDB
Juglans nigra L.	FooDB	FooDB
Juglans regia	FooDB	FooDB
Lablab purpureus	FooDB	FooDB
Lactuca sativa	FooDB	FooDB
Lagenaria siceraria	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Lathyrus sativus	FooDB	FooDB
Laurus nobilis L.	FooDB	FooDB
Lens culinaris	FooDB	FooDB
Lentinus edodes	FooDB	FooDB
Lepidium sativum	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Levisticum officinale	FooDB	FooDB
Linum usitatissimum	FooDB	FooDB
Litchi chinensis	FooDB	FooDB
Luffa aegyptiaca	FooDB	FooDB
Lupinus	FooDB	FooDB
Lupinus albus	FooDB	FooDB
Macadamia	FooDB	FooDB
Macadamia tetraphylla	FooDB	FooDB
Malpighia emarginata	FooDB	FooDB
Malus	FooDB	FooDB
Malus pumila	FooDB	FooDB
Mammea americana	FooDB	FooDB
Mangifera indica	FooDB	FooDB
Manihot esculenta	FooDB	FooDB
Manilkara zapota	FooDB	FooDB
Maranta arundinacea	FooDB	FooDB
Matricaria recutita	FooDB	FooDB
Matteuccia struthiopteris	FooDB	FooDB
Medicago sativa	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Melissa officinalis L.	FooDB	FooDB
Mentha	FooDB	FooDB
Mentha aquatica	FooDB	FooDB
Mentha arvensis	FooDB	FooDB
Mentha spicata	FooDB	FooDB
Mentha x piperita	FooDB	FooDB
Mespilus germanica	FooDB	FooDB
Metroxylon sagu	FooDB	FooDB
Momordica charantia	FooDB	FooDB
Morchellaceae	FooDB	FooDB
Morella rubra	FooDB	FooDB
Moringa oleifera	FooDB	FooDB
Morus	FooDB	FooDB
Morus nigra	FooDB	FooDB
Musa acuminata	FooDB	FooDB
Musa x paradisiaca	FooDB	FooDB
Myrica	FooDB	FooDB
Myristica fragrans	FooDB	FooDB
Mytilus edulis	LOTUS Database	35616633
Nelumbo	FooDB	FooDB
Nelumbo nucifera	FooDB	FooDB
Nephelium lappaceum	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Nuphar lutea	FooDB	FooDB
Ocimum basilicum	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oenothera biennis	FooDB	FooDB
Olea europaea	FooDB	FooDB
Opuntia	FooDB	FooDB
Opuntia cochenillifera	FooDB	FooDB
Opuntia macrorhiza	FooDB	FooDB
Origanum majorana	FooDB	FooDB
Origanum onites	FooDB	FooDB
Origanum vulgare	FooDB	FooDB
Origanum X majoricum	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Oryza rufipogon	FooDB	FooDB
Oryza sativa	FooDB	FooDB
Ovis aries	FooDB	FooDB
Pachyrhizus erosus	FooDB	FooDB
Panax ginseng	FooDB	FooDB
Pangium edule	FooDB	FooDB
Panicum miliaceum	FooDB	FooDB
Passiflora edulis	FooDB	FooDB
Pastinaca sativa	FooDB	FooDB
Pediomelum esculentum	FooDB	FooDB
Perideridia oregana	FooDB	FooDB
Persea americana	FooDB	FooDB
Petasites japonicus	FooDB	FooDB
Petroselinum crispum	FooDB	FooDB
Phaseolus coccineus	FooDB	FooDB
Phaseolus lunatus	FooDB	FooDB
Phaseolus vulgaris	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Phoenix dactylifera	FooDB	FooDB
Photinia melanocarpa	FooDB	FooDB
Phyllostachys edulis	FooDB	FooDB
Physalis	FooDB	FooDB
Physalis philadelphica var. immaculata	FooDB	FooDB
Phytolacca americana	FooDB	FooDB
Pimenta dioica	FooDB	FooDB
Pimpinella anisum	FooDB	FooDB
Pinus	FooDB	FooDB
Pinus edulis	FooDB	FooDB
Piper nigrum L.	FooDB	FooDB
Pistacia vera	FooDB	FooDB
Pisum sativum	FooDB	FooDB
Pleurotus ostreatus	FooDB	FooDB
Polygonum alpinum	FooDB	FooDB
Portulaca oleracea	FooDB	FooDB
Pouteria sapota	FooDB	FooDB
Prunus armeniaca	FooDB	FooDB
Prunus avium	FooDB	FooDB
Prunus avium L.	FooDB	FooDB
Prunus cerasus	FooDB	FooDB
Prunus domestica	FooDB	FooDB
Prunus dulcis	FooDB	FooDB
Prunus persica	FooDB	FooDB
Prunus persica var. nucipersica	FooDB	FooDB
Prunus persica var. persica	FooDB	FooDB
Prunus tomentosa	FooDB	FooDB
Prunus virginiana	FooDB	FooDB
Psidium cattleianum	FooDB	FooDB
Psidium guajava	FooDB	FooDB
Psophocarpus tetragonolobus	FooDB	FooDB
Punica granatum	FooDB	FooDB
Pyrus communis	FooDB	FooDB
Pyrus pyrifolia	FooDB	FooDB
Quercus	FooDB	FooDB
Raphanus sativus	FooDB	FooDB
Raphanus sativus var. longipinnatus	FooDB	FooDB
Raphanus sativus var. sativus	FooDB	FooDB
Rheum rhabarbarum	FooDB	FooDB
Ribes aureum	FooDB	FooDB
Ribes glandulosum	FooDB	FooDB
Ribes nigrum	FooDB	FooDB
Ribes rubrum	FooDB	FooDB
Ribes uva-crispa	FooDB	FooDB
Rosa	FooDB	FooDB
Rubus arcticus	FooDB	FooDB
Rubus chamaemorus	FooDB	FooDB
Rubus idaeus	FooDB	FooDB
Rubus occidentalis	FooDB	FooDB
Rubus spectabilis	FooDB	FooDB
Rumex	FooDB	FooDB
Rumex acetosa	FooDB	FooDB
Rumex articus	FooDB	FooDB
Sagittaria latifolia	FooDB	FooDB
Salix pulchra	FooDB	FooDB
Salvia elegans	FooDB	FooDB
Salvia hispanica	FooDB	FooDB
Salvia officinalis	FooDB	FooDB
Salvia rosmarinus	FooDB	FooDB
Sambucus nigra	FooDB	FooDB
Sambucus nigra L.	FooDB	FooDB
Satureja hortensis L.	FooDB	FooDB
Satureja montana	FooDB	FooDB
Scorzonera hispanica	FooDB	FooDB
Secale cereale	FooDB	FooDB
Sechium edule	FooDB	FooDB
Sesamum indicum	FooDB	FooDB
Sesbania bispinosa	FooDB	FooDB
Sinapis alba	FooDB	FooDB
Sisymbrium	FooDB	FooDB
Solanum glaucophyllum	LOTUS Database	35616633
Solanum lycopersicum	FooDB	FooDB
Solanum lycopersicum var. cerasiforme	FooDB	FooDB
Solanum lycopersicum var. lycopersicum	FooDB	FooDB
Solanum melongena	FooDB	FooDB
Solanum quitoense	FooDB	FooDB
Solanum tuberosum	FooDB	FooDB
Sorbus aucuparia	FooDB	FooDB
Sorghum bicolor	FooDB	FooDB
Spinacia oleracea	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB
Syzygium aromaticum	FooDB	FooDB
Syzygium cumini	FooDB	FooDB
Syzygium jambos	FooDB	FooDB
Tamarindus indica	FooDB	FooDB
Taraxacum officinale	FooDB	FooDB
Tetragonia tetragonioides	FooDB	FooDB
Thelesperma	FooDB	FooDB
Thymus pulegioides	FooDB	FooDB
Thymus vulgaris	FooDB	FooDB
Tilia cordata	FooDB	FooDB
Tilia L.	FooDB	FooDB
Tragopogon porrifolius	FooDB	FooDB
Trigonella foenum-graecum	FooDB	FooDB
Triticum	FooDB	FooDB
Triticum aestivum	FooDB	FooDB
Triticum durum	FooDB	FooDB
Triticum spelta	FooDB	FooDB
Triticum turanicum	FooDB	FooDB
Typha angustifolia	FooDB	FooDB
Vaccinium	FooDB	FooDB
Vaccinium angustifolium	FooDB	FooDB
Vaccinium angustifolium X Vaccinium corymbosum	FooDB	FooDB
Vaccinium arboreum	FooDB	FooDB
Vaccinium corymbosum	FooDB	FooDB
Vaccinium deliciosum	FooDB	FooDB
Vaccinium elliottii	FooDB	FooDB
Vaccinium macrocarpon	FooDB	FooDB
Vaccinium myrtilloides	FooDB	FooDB
Vaccinium myrtillus	FooDB	FooDB
Vaccinium ovalifolium	FooDB	FooDB
Vaccinium ovatum	FooDB	FooDB
Vaccinium oxycoccos	FooDB	FooDB
Vaccinium parvifolium	FooDB	FooDB
Vaccinium reticulatum	FooDB	FooDB
Vaccinium stamineum	FooDB	FooDB
Vaccinium uliginosum	FooDB	FooDB
Vaccinium vitis-idaea	FooDB	FooDB
Valerianella locusta	FooDB	FooDB
Vanilla	FooDB	FooDB
Verbena officinalis	FooDB	FooDB
Viburnum edule	FooDB	FooDB
Vicia faba	FooDB	FooDB
Vigna aconitifolia	FooDB	FooDB
Vigna angularis	FooDB	FooDB
Vigna mungo	FooDB	FooDB
Vigna radiata	FooDB	FooDB
Vigna umbellata	FooDB	FooDB
Vigna unguiculata	FooDB	FooDB
Vigna unguiculata ssp. cylindrica	FooDB	FooDB
Vigna unguiculata ssp. unguiculata	FooDB	FooDB
Vigna unguiculata var. sesquipedalis	FooDB	FooDB
Vitis	FooDB	FooDB
Vitis aestivalis	FooDB	FooDB
Vitis labrusca	FooDB	FooDB
Vitis rotundifolia	FooDB	FooDB
Vitis vinifera L.	FooDB	FooDB
Xanthosoma sagittifolium	FooDB	FooDB
Zea mays L.	FooDB	FooDB
Zingiber officinale	FooDB	FooDB
Zizania	FooDB	FooDB
Zizania aquatica	FooDB	FooDB
Ziziphus zizyphus	FooDB	FooDB

Species Where Detected

Species Name	Source	Reference
Lactarius sp.	KNApSAcK Database	22123792
Nectria galligena	KNApSAcK Database	22123792
Russula aeruginosa	KNApSAcK Database	22123792
Russula decolorans	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol
Cholesterol-skeleton
3-hydroxy-delta-5-steroid
3-hydroxy-delta-7-steroid
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
3-hydroxysteroid
Hydroxysteroid
Delta-7-steroid
Delta-5-steroid
Cyclic alcohol
Secondary alcohol
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

cholestanoid (CHEBI:17759 )
3beta-sterol (CHEBI:17759 )
Vitamin D3 and derivatives (C01164 )
Cholestane and derivatives (C01164 )
Cholesterol and derivatives (LMST01010069 )

Physical Properties

State

Solid

Experimental Properties

Property	Value	Reference
Melting Point	150.5 °C	Not Available
Boiling Point	493.70 °C. @ 760.00 mm Hg (est)	The Good Scents Company Information System
Water Solubility	1 mg/mL	Not Available
LogP	9.460 (est)	The Good Scents Company Information System

Predicted Properties

Property	Value	Source
Water Solubility	0.00015 g/L	ALOGPS
logP	7.3	ALOGPS
logP	6.71	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	18.27	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	121.47 m³·mol⁻¹	ChemAxon
Polarizability	50.01 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0000032

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

7-Dehydrocholesterol

METLIN ID

Not Available

PubChem Compound

439423

PDB ID

Not Available

ChEBI ID

17759

Good Scents ID

rw1136601

References

General References

Lehmann B, Genehr T, Knuschke P, Pietzsch J, Meurer M: UVB-induced conversion of 7-dehydrocholesterol to 1alpha,25-dihydroxyvitamin D3 in an in vitro human skin equivalent model. J Invest Dermatol. 2001 Nov;117(5):1179-85. [PubMed:11710930 ]
Muzzin KB, Harper LF: Smith-Lemli-Opitz syndrome: a review, case report and dental implications. Spec Care Dentist. 2003;23(1):22-7. [PubMed:12887150 ]
Paterson CR, Moody JP, Pennington CR: Skin content of 7-dehydrocholesterol in patients with malabsorption. Nutrition. 1997 Sep;13(9):771-3. [PubMed:9290088 ]
Jira PE, Wevers RA, de Jong J, Rubio-Gozalbo E, Janssen-Zijlstra FS, van Heyst AF, Sengers RC, Smeitink JA: Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndrome. J Lipid Res. 2000 Aug;41(8):1339-46. [PubMed:10946022 ]
Johnson DW, ten Brink HJ, Jakobs C: A rapid screening procedure for cholesterol and dehydrocholesterol by electrospray ionization tandem mass spectrometry. J Lipid Res. 2001 Oct;42(10):1699-705. [PubMed:11590227 ]
van Rooij A, Nijenhuis AA, Wijburg FA, Schutgens RB: Highly increased CSF concentrations of cholesterol precursors in Smith-Lemli-Opitz syndrome. J Inherit Metab Dis. 1997 Aug;20(4):578-80. [PubMed:9266395 ]
Andersson HC, Frentz J, Martinez JE, Tuck-Muller CM, Bellizaire J: Adrenal insufficiency in Smith-Lemli-Opitz syndrome. Am J Med Genet. 1999 Feb 19;82(5):382-4. [PubMed:10069708 ]
GarciaFuentes E, icioso Recio MV, del Castillo Acedo Del Olmo E, atas Jurado MM, Arana Aguera M, Lopez Lopez J: [Biochemical diagnosis of Smith-Lemli-Opitz syndrome in a patient with congenital adrenal hyperplasia]. An Esp Pediatr. 2000 Nov;53(5):482-7. [PubMed:11141372 ]
Jezela-Stanek A, Malunowicz EM, Ciara E, Popowska E, Goryluk-Kozakiewicz B, Spodar K, Czerwiecka M, Jezuita J, Nowaczyk MJ, Krajewska-Walasek M: Maternal urinary steroid profiles in prenatal diagnosis of Smith-Lemli-Opitz syndrome: first patient series comparing biochemical and molecular studies. Clin Genet. 2006 Jan;69(1):77-85. [PubMed:16451140 ]
Moody JP, Humphries CA, Allan SM, Paterson CR: Determination of 7-dehydrocholesterol in human skin by high-performance liquid chromatography. J Chromatogr. 1990 Aug 24;530(1):19-27. [PubMed:2277111 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
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Showing NP-Card for 7-Dehydrocholesterol (NP0000147)

MOL for NP0000147 (7-Dehydrocholesterol)

3D MOL for NP0000147 (7-Dehydrocholesterol)

3D SDF for NP0000147 (7-Dehydrocholesterol)

3D-SDF for NP0000147 (7-Dehydrocholesterol)

PDB for NP0000147 (7-Dehydrocholesterol)

3D PDB for NP0000147 (7-Dehydrocholesterol)

SMILES for NP0000147 (7-Dehydrocholesterol)

INCHI for NP0000147 (7-Dehydrocholesterol)

Structure for NP0000147 (7-Dehydrocholesterol)

3D Structure for NP0000147 (7-Dehydrocholesterol)