NP-MRD: Showing NP-Card for (1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid (NP0270378)

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Record Information

Version

2.0

Created at

2022-09-08 16:14:48 UTC

Updated at

2022-09-08 16:14:49 UTC

NP-MRD ID

NP0270378

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid

Description

(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosane-5,18-dicarboxylic acid belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. (1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid is found in Schefflera heptaphylla. Based on a literature review very few articles have been published on (1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosane-5,18-dicarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082218142D          

 35 39  0  0  1  0            999 V2000
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    4.2522   -2.4226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 15 35  1  0  0  0  0
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  7 35  1  0  0  0  0
M  END

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M  END


  Mrv1652309082218142D          

 35 39  0  0  1  0            999 V2000
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    9.9241   -0.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8505   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9814   -0.2334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4905   -1.5685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5030   -2.0500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.3279   -2.0374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1014   -2.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2765   -2.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8532   -2.0750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4516   -2.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5536   -2.1252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  6  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  1  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 14 12  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  6  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 23 33  1  0  0  0  0
 18 33  1  0  0  0  0
 33 34  1  1  0  0  0
 15 35  1  0  0  0  0
 35  4  1  1  0  0  0
  7 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270378

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O5/c1-16(2)18-9-14-30(26(34)35)15-17(3)23-19(24(18)30)7-8-20-27(4)13-11-22(31)29(6,25(32)33)21(27)10-12-28(20,23)5/h17-24,31H,1,7-15H2,2-6H3,(H,32,33)(H,34,35)/t17-,18-,19-,20-,21-,22+,23+,24+,27+,28+,29-,30-/m0/s1

> <INCHI_KEY>
LZRAEABBGSAANR-OLWGDLAQSA-N

> <FORMULA>
C30H46O5

> <MOLECULAR_WEIGHT>
486.693

> <EXACT_MASS>
486.334524581

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
55.11387543452893

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

> <JCHEM_LOGP>
5.818403655333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.979672497851465

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.36431534028291

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0375459247194874

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
134.41619999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       8.568  -7.676   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.697  -6.628   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.168  -7.082   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.354  -5.127   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.937  -4.522   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.075  -2.988   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.576  -2.645   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.652  -1.413   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.257   0.003   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       7.123  -1.598   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.326  -1.300   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.866  -1.277   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.616   0.069   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.656  -2.598   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.906  -3.944   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.697  -5.265   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.236  -5.242   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.986  -3.897   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.196  -2.575   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.406  -1.253   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.946  -1.230   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.485  -1.206   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      17.276  -2.528   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.815  -2.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.525  -0.992   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      20.254  -1.956   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      20.499  -0.436   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      21.449  -2.928   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      19.606  -3.827   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      21.145  -3.803   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      18.856  -5.172   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      17.316  -5.195   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.526  -3.873   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.776  -5.219   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.367  -3.967   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   35                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11   35                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16   35                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   33                                                  
CONECT   19   18   14   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   33                                                  
CONECT   24   23   25   26   29                                             
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   23   18   34                                             
CONECT   34   33                                                            
CONECT   35   15    4    7                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-Hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0,.0,.0,]henicosane-5,18-dicarboxylate	Generator

Chemical Formula

C₃₀H₄₆O₅

Average Mass

486.6930 Da

Monoisotopic Mass

486.33452 Da

IUPAC Name

(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

Traditional Name

(1S,2R,3S,5S,8R,9S,10S,13R,14R,17R,18S,19S)-17-hydroxy-1,3,14,18-tetramethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C30H46O5/c1-16(2)18-9-14-30(26(34)35)15-17(3)23-19(24(18)30)7-8-20-27(4)13-11-22(31)29(6,25(32)33)21(27)10-12-28(20,23)5/h17-24,31H,1,7-15H2,2-6H3,(H,32,33)(H,34,35)/t17-,18-,19-,20-,21-,22+,23+,24+,27+,28+,29-,30-/m0/s1

InChI Key

LZRAEABBGSAANR-OLWGDLAQSA-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
Heptapleurum heptaphyllum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

18-hydroxysteroid
18-oxosteroid
Estrane-skeleton
Oxosteroid
Hydroxysteroid
15-hydroxysteroid
Beta-hydroxy acid
Dicarboxylic acid or derivatives
Hydroxy acid
Cyclic alcohol
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
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	5.82	ChemAxon
pKa (Strongest Acidic)	4.36	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	134.42 m³·mol⁻¹	ChemAxon
Polarizability	55.11 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

163043024

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid (NP0270378)

MOL for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D MOL for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D SDF for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D-SDF for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

PDB for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D PDB for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

SMILES for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

INCHI for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

Structure for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D Structure for NP0270378 ((1r,3as,5s,5ar,5bs,7as,8s,9r,11ar,11br,13as,13bs)-9-hydroxy-5,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydro-1h-cyclopenta[a]chrysene-3a,8-dicarboxylic acid)