NP-MRD: Showing NP-Card for (4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol (NP0161040)

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Record Information

Version

2.0

Created at

2022-09-02 19:08:04 UTC

Updated at

2022-09-02 19:08:04 UTC

NP-MRD ID

NP0161040

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol

Description

(20Z)-4,4,8-Trimethyl-D(15),24-dinor-13,17-seco-5alpha-chola-13(18),20(22)-diene-1beta,6alpha,23-triol belongs to the class of organic compounds known as cheilanthane sesterterpenoids. These are sesterterpnoids with a structure based on the cheilanthane backbone. Cheilanthane is a tricyclic compound consisting of a tetradecahydrophenanthrene ring system that carries two methyl groups at the 1-position, one methyl group at the 4a-,7-, and 8a-positions, as well as a 3-methylpentyl group at the 8-position. (4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol is found in Aleuritopteris farinosa. Based on a literature review very few articles have been published on (20Z)-4,4,8-Trimethyl-D(15),24-dinor-13,17-seco-5alpha-chola-13(18),20(22)-diene-1beta,6alpha,23-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022221082D          

 28 30  0  0  1  0            999 V2000
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 11  9  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 11 19  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  1  0  0  0
  6 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 70 72  0  0  0  0  0  0  0  0999 V2000
    2.2770   -1.9004    1.9494 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5758   -1.6644    0.8602 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8648   -2.8052    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5278   -2.3898   -0.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8148   -0.9871    0.3297 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1357   -0.0596   -0.3348 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.6472    1.5682   -0.6396 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.4809    0.8530    0.3647 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9146    1.2562    0.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9520    2.6846    0.9120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4389    1.3940   -1.1028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8328    0.4333    1.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8870   -1.0834    1.6670 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6333   -2.4161    1.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2441   -0.6393    0.3368 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0327   -1.3500   -0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5055   -0.2813    0.3185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6265   -0.0065   -0.6156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9715   -0.1583    0.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0865    0.1072   -0.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1681   -0.8127   -2.0128 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9961    1.0367   -0.7146 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0243    1.9978    0.4031 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2447    1.8551    1.0940 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3234   -2.9109    2.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7902   -1.0842    2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8178   -3.6266    0.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3944   -3.2108   -0.6690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6734   -2.4391   -1.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2389   -3.1033    0.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4881   -1.0724    1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8588   -1.3074   -2.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0257    0.4473   -2.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536   -0.3314   -2.4188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4608    1.9773   -0.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1525    1.7106    0.8715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7208    1.1155   -1.6522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1559    3.4813   -0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0930    1.1829    1.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1005    3.4404    0.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8060    2.7992    1.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0477    2.9284    1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6610    2.4502   -1.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7354    1.0267   -1.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4422    0.8776   -1.1801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7666    0.2412    0.5391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2488    0.9986    2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7212   -1.0856    2.6904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8017   -1.7284    1.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4002   -0.4354    2.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4965   -2.5868    2.8961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0470   -2.4448   -0.4382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0904   -1.0523   -0.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6441   -1.2806   -1.7253 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5867    0.4202    1.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6960   -0.6687   -1.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6375    1.0282   -1.0119 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1015   -1.2216    0.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9457    0.4300    1.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2013   -0.8627   -2.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8693   -1.8405   -1.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5198   -0.4403   -2.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7715    1.1023   -1.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9583    2.3654    0.6369 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
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 17 18  1  0
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 19 20  1  6
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  6 21  1  0
 19 11  1  0
 19  5  1  0
 25 64  1  0
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 23 62  1  0
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 22 61  1  0
 21 59  1  1
  1 29  1  0
  1 30  1  0
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  9 41  1  6
 10 42  1  0
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 26 67  1  0
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 27 69  1  0
 28 70  1  0
M  END


  Mrv1652309022221082D          

 28 30  0  0  1  0            999 V2000
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
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 17 19  1  0  0  0  0
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 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161040

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CC[C@@H]1C(=C)CC[C@H]2[C@@]1(C)C[C@H](O)[C@H]1C(C)(C)CC[C@@H](O)[C@]21C)=C\CO

> <INCHI_IDENTIFIER>
InChI=1S/C25H42O3/c1-16(12-14-26)7-9-18-17(2)8-10-20-24(18,5)15-19(27)22-23(3,4)13-11-21(28)25(20,22)6/h12,18-22,26-28H,2,7-11,13-15H2,1,3-6H3/b16-12-/t18-,19+,20+,21-,22+,24+,25+/m1/s1

> <INCHI_KEY>
XUMCBOHALFECLC-KXARRXHNSA-N

> <FORMULA>
C25H42O3

> <MOLECULAR_WEIGHT>
390.608

> <EXACT_MASS>
390.313395212

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
46.83165359739955

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,4aR,4bS,8R,8aS,10S,10aS)-8-[(3Z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-tetradecahydrophenanthrene-4,10-diol

> <ALOGPS_LOGP>
4.03

> <JCHEM_LOGP>
3.919231322333334

> <ALOGPS_LOGS>
-4.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.09039242163098

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.471460172093213

> <JCHEM_PKA_STRONGEST_BASIC>
-2.217044720353715

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
116.13389999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.55e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,4aR,4bS,8R,8aS,10S,10aS)-8-[(3Z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.954  -1.897   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.874   3.437   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.804  -3.231   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.034  -4.565   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.344  -3.231   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.114  -1.897   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.344  -0.564   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7    8   21                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   19                                                  
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   11    5   20                                             
CONECT   20   19                                                            
CONECT   21    6    2   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
(20Z)-4,4,8-Trimethyl-D(15),24-dinor-13,17-seco-5a-chola-13(18),20(22)-diene-1b,6a,23-triol	Generator
(20Z)-4,4,8-Trimethyl-D(15),24-dinor-13,17-seco-5α-chola-13(18),20(22)-diene-1β,6α,23-triol	Generator

Chemical Formula

C₂₅H₄₂O₃

Average Mass

390.6080 Da

Monoisotopic Mass

390.31340 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C(CC[C@@H]1C(=C)CC[C@H]2[C@@]1(C)C[C@H](O)[C@H]1C(C)(C)CC[C@@H](O)[C@]21C)=C\CO

InChI Identifier

InChI=1S/C25H42O3/c1-16(12-14-26)7-9-18-17(2)8-10-20-24(18,5)15-19(27)22-23(3,4)13-11-21(28)25(20,22)6/h12,18-22,26-28H,2,7-11,13-15H2,1,3-6H3/b16-12-/t18-,19+,20+,21-,22+,24+,25+/m1/s1

InChI Key

XUMCBOHALFECLC-KXARRXHNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Aleuritopteris farinosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cheilanthane sesterterpenoids. These are sesterterpnoids with a structure based on the cheilanthane backbone. Cheilanthane is a tricyclic compound consisting of a tetradecahydrophenanthrene ring system that carries two methyl groups at the 1-position, one methyl group at the 4a-,7-, and 8a-positions, as well as a 3-methylpentyl group at the 8-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Cheilanthane sesterterpenoids

Alternative Parents

Substituents

Cheilanthane sesterterpenoid
1-hydroxysteroid
6-hydroxysteroid
Hydroxysteroid
Steroid
Hydrophenanthrene
Phenanthrene
Fatty alcohol
Fatty acyl
Cyclic alcohol
Secondary alcohol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.03	ALOGPS
logP	3.92	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	14.47	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15767749

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol (NP0161040)

MOL for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

3D MOL for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

3D SDF for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

3D-SDF for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

PDB for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

3D PDB for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

SMILES for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

INCHI for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

Structure for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)

3D Structure for NP0161040 ((4r,4ar,4bs,8r,8as,10s,10as)-8-[(3z)-5-hydroxy-3-methylpent-3-en-1-yl]-1,1,4a,8a-tetramethyl-7-methylidene-decahydrophenanthrene-4,10-diol)