NP-MRD: Showing NP-Card for 7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol (NP0316248)

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Record Information

Version

2.0

Created at

2022-09-11 15:18:57 UTC

Updated at

2022-09-11 15:18:58 UTC

NP-MRD ID

NP0316248

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol

Description

7,7-Bis(hydroxymethyl)-3',3',4a,4b,10a-pentamethyl-3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b,11-tetradecahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol belongs to the class of organic compounds known as 12-hydroxysteroids. These are steroids carrying a hydroxyl group at the 12-position of the steroid backbone. 7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol is found in Phlomis umbrosa. 7,7-Bis(hydroxymethyl)-3',3',4a,4b,10a-pentamethyl-3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b,11-tetradecahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004191518512D          

 34 38  0  0  0  0            999 V2000
    6.8995    1.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6205    0.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4218    0.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5091   -0.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6972   -0.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069    0.5073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9947    1.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1773    1.3825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6720    0.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3598    1.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4790   -0.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6615   -0.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3493    0.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5319    0.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8441   -0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0267   -0.3512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2092   -0.2397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2960   -0.8919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030    0.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9204    0.6354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023    1.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277    1.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3599    2.3849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6540    1.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0995    2.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2197    1.0647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7250    1.7169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424    1.6054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546    0.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8800    1.6663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8016   -0.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1138   -0.9085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8776    1.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 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  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 11 32  1  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 34  1  0  0  0  0
  2 34  1  0  0  0  0
M  END


  Mrv1533004191518512D          

 34 38  0  0  0  0            999 V2000
    6.8995    1.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6205    0.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4218    0.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5091   -0.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6972   -0.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3069    0.5073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9947    1.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1773    1.3825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6720    0.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3598    1.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4790   -0.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6615   -0.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3493    0.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5319    0.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8441   -0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0267   -0.3512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2092   -0.2397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2960   -0.8919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1030    0.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9204    0.6354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023    1.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277    1.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3599    2.3849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6540    1.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0995    2.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2197    1.0647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7250    1.7169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424    1.6054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546    0.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8800    1.6663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8016   -0.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1138   -0.9085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8776    1.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 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  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 11 32  1  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 34  1  0  0  0  0
  2 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316248

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC2(C1)CCC1(C)C(=CCC3C4(C)CC(O)C(O)C(CO)(CO)C4CCC13C)C2O

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O5/c1-24(2)10-12-28(15-24)13-11-26(4)18(22(28)33)6-7-20-25(3)14-19(32)23(34)29(16-30,17-31)21(25)8-9-27(20,26)5/h6,19-23,30-34H,7-17H2,1-5H3

> <INCHI_KEY>
KOXCHMHNDGJSRT-UHFFFAOYSA-N

> <FORMULA>
C29H48O5

> <MOLECULAR_WEIGHT>
476.698

> <EXACT_MASS>
476.350174646

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
55.52652878707899

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b,11-tetradecahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol

> <ALOGPS_LOGP>
3.24

> <JCHEM_LOGP>
2.404772210666667

> <ALOGPS_LOGS>
-4.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.596284827047135

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.4769832842827

> <JCHEM_PKA_STRONGEST_BASIC>
-0.38148115276243344

> <JCHEM_POLAR_SURFACE_AREA>
101.15

> <JCHEM_REFRACTIVITY>
133.6311

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      12.879   2.839   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.358   1.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.854   1.023   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.150  -0.136   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.635  -0.410   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.906   0.947   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.323   2.372   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.798   2.581   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.854   1.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.272   2.789   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.437  -0.062   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.494  -1.280   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.968  -1.072   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.385   0.354   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.860   0.562   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.442  -0.864   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.916  -0.655   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.391  -0.447   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.553  -1.665   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.192   0.978   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.718   1.186   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.751   2.195   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.612   2.913   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.672   4.452   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.221   3.662   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.186   4.802   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.277   1.987   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.220   3.205   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.746   2.997   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.329   1.571   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.376   3.111   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.963  -0.270   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.546  -1.696   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      10.971   2.059   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   34                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   32   34                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   30                                             
CONECT   10    9                                                            
CONECT   11    9   12   32                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   30                                                  
CONECT   15   14   16   17   27                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25   27                                             
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25                                                            
CONECT   27   22   15   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    9   14   31                                             
CONECT   31   30                                                            
CONECT   32   11    6   33                                                  
CONECT   33   32                                                            
CONECT   34    6    2                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₈O₅

Average Mass

476.6980 Da

Monoisotopic Mass

476.35017 Da

IUPAC Name

7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b,11-tetradecahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol

Traditional Name

7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol

CAS Registry Number

Not Available

SMILES

CC1(C)CCC2(C1)CCC1(C)C(=CCC3C4(C)CC(O)C(O)C(CO)(CO)C4CCC13C)C2O

InChI Identifier

InChI=1S/C29H48O5/c1-24(2)10-12-28(15-24)13-11-26(4)18(22(28)33)6-7-20-25(3)14-19(32)23(34)29(16-30,17-31)21(25)8-9-27(20,26)5/h6,19-23,30-34H,7-17H2,1-5H3

InChI Key

KOXCHMHNDGJSRT-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Phlomis umbrosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 12-hydroxysteroids. These are steroids carrying a hydroxyl group at the 12-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

12-hydroxysteroids

Alternative Parents

Substituents

12-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Polyol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
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	3.24	ALOGPS
logP	2.4	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	13.48	ChemAxon
pKa (Strongest Basic)	-0.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	101.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	133.63 m³·mol⁻¹	ChemAxon
Polarizability	55.53 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol (NP0316248)

MOL for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

3D MOL for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

3D SDF for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

3D-SDF for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

PDB for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

3D PDB for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

SMILES for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

INCHI for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

Structure for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)

3D Structure for NP0316248 (7,7-bis(hydroxymethyl)-4',4',4a,4b,10a-pentamethyl-3,4,5,6,6a,8,9,10,10b,11-decahydro-1h-spiro[chrysene-2,1'-cyclopentane]-1,8,9-triol)