NP-MRD: Showing NP-Card for 4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol (NP0256408)

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Record Information

Version

2.0

Created at

2022-09-07 21:13:39 UTC

Updated at

2022-09-07 21:13:39 UTC

NP-MRD ID

NP0256408

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol

Description

ACon1_000901 belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). Based on a literature review very few articles have been published on ACon1_000901.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223132D          

 27 30  0  0  0  0            999 V2000
    1.4460   -1.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335   -0.7783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085   -0.7783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2040   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2040    1.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8359    0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8359    1.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6112    1.6133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    2.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335    2.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4460    1.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8585    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4460   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2710   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9691    1.0632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    1.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    2.7132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125    1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8270    1.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8270    2.7132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    0.2382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980   -0.5868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    0.5283   -2.6255   -0.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3523   -1.6389   -0.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3822   -2.1694    0.5583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2755   -1.1965    1.2315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7089   -0.2163    0.1280 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5464    0.5487   -0.4072 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6964    0.6030   -1.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4475    1.9451    0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0172    2.0812    1.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3817    1.5427    1.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8301    0.5834    0.6715 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8183   -0.3885    1.3375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6526    1.3174   -0.3530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2482    0.4413   -1.2807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2125   -0.1818   -0.1758 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8482    0.2980   -1.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2401   -0.1439   -0.8213 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0877    0.5084   -1.8940 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1688   -0.8340   -1.5605 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4441   -1.1770   -0.8258 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3200   -2.2325    0.0401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0361    0.0412   -0.2062 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4573    0.4272   -0.3146 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2117   -0.6084    0.2420 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1717    0.7938    0.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7846    0.3332    0.5340 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6486   -0.7483    1.4332 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4807   -2.8049   -0.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7235   -2.3466   -1.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0310   -3.6394   -0.8480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5281   -3.2381    0.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7457   -0.7003    2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1489   -1.7438    1.5778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1341   -0.8895   -0.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0174    1.3676   -2.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7176    0.8949   -2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5233   -0.4027   -2.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8486    2.7191   -0.5549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3637    2.2184    0.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0281    3.1662    1.7749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2692    1.6412    2.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1534    2.3542    1.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4199    1.0221    2.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8379    0.1021    1.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5687   -0.5468    2.4050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9507   -1.2949    0.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5308    1.7411    0.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1668    2.1676   -0.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8311    1.0389   -1.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0893    0.1389    0.8669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5065    0.0248   -2.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8686    1.4181   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9247   -1.5951   -2.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1826   -1.4953   -1.6192 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2017   -2.7145    0.1182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7698    0.6309   -1.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6316    1.3134    0.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8680   -0.2786    0.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5028    1.7047    0.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624    1.1386    0.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4636   -0.4158    2.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  6
  6 15  1  0
 15 16  1  0
 17 16  1  6
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  2  0
 25 26  1  0
 26 27  1  0
 15  2  1  0
 19 17  1  0
  6  5  1  0
 26 17  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
 12 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 10 42  1  0
 10 43  1  0
  9 40  1  0
  9 41  1  0
  8 38  1  0
  8 39  1  0
  7 35  1  0
  7 36  1  0
  7 37  1  0
 15 50  1  1
 16 51  1  0
 16 52  1  0
 19 53  1  6
 20 54  1  6
 21 55  1  0
 23 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
 26 60  1  1
 27 61  1  0
M  END


  Mrv1652309072223132D          

 27 30  0  0  0  0            999 V2000
    1.4460   -1.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335   -0.7783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085   -0.7783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2040   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2040    1.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8359    0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8359    1.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6112    1.6133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    2.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335    2.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4460    1.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8585    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4460   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2710   -0.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9691    1.0632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    1.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    2.7132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125    1.4757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8270    1.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8270    2.7132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125    0.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980    0.2382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3980   -0.5868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256408

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CCC2C(C)(CO)CCCC2(C)C1CC12OC1C(O)C(CO)=CC2O

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O5/c1-13-5-6-16-20(2,12-24)7-4-8-21(16,3)15(13)10-22-17(25)9-14(11-23)18(26)19(22)27-22/h5,9,15-19,23-26H,4,6-8,10-12H2,1-3H3

> <INCHI_KEY>
ADIALAZTBGIRSN-UHFFFAOYSA-N

> <FORMULA>
C22H34O5

> <MOLECULAR_WEIGHT>
378.509

> <EXACT_MASS>
378.240624195

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
42.4718545382782

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol

> <JCHEM_LOGP>
1.0220679243333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.777727336572227

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.160593237577196

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2010084527307812

> <JCHEM_POLAR_SURFACE_AREA>
93.45

> <JCHEM_REFRACTIVITY>
104.19689999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       2.699  -2.786   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.929  -1.453   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.389  -1.453   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.381  -0.119   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.389   1.215   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.381   2.548   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.560   1.558   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.560   3.538   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.008   3.011   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.389   3.882   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.929   3.882   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.699   2.548   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.929   1.215   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.469   1.215   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.699  -0.119   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.239  -0.119   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.009   1.215   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.676   1.985   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.009   2.755   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.343   3.525   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.343   5.065   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.677   2.755   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.010   3.525   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.010   5.065   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.677   1.215   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.343   0.445   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.343  -1.095   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7    8   10                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8                                                            
CONECT   10    6   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    5   14   15                                             
CONECT   14   13                                                            
CONECT   15   13    2   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19   26                                             
CONECT   18   17   19                                                       
CONECT   19   18   17   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   17   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₅

Average Mass

378.5090 Da

Monoisotopic Mass

378.24062 Da

IUPAC Name

4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol

Traditional Name

4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol

CAS Registry Number

Not Available

SMILES

CC1=CCC2C(C)(CO)CCCC2(C)C1CC12OC1C(O)C(CO)=CC2O

InChI Identifier

InChI=1S/C22H34O5/c1-13-5-6-16-20(2,12-24)7-4-8-21(16,3)15(13)10-22-17(25)9-14(11-23)18(26)19(22)27-22/h5,9,15-19,23-26H,4,6-8,10-12H2,1-3H3

InChI Key

ADIALAZTBGIRSN-UHFFFAOYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Secondary alcohols

Alternative Parents

Substituents

Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Hydrocarbon derivative
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.02	ChemAxon
pKa (Strongest Acidic)	13.16	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	93.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	104.2 m³·mol⁻¹	ChemAxon
Polarizability	42.47 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

23550468

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23930356

PDB ID

Not Available

ChEBI ID

182483

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol (NP0256408)

MOL for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

3D MOL for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

3D SDF for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

3D-SDF for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

PDB for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

3D PDB for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

SMILES for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

INCHI for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

Structure for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)

3D Structure for NP0256408 (4-(hydroxymethyl)-1-{[5-(hydroxymethyl)-2,5,8a-trimethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl}-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol)