NP-MRD: Showing NP-Card for (3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid (NP0303553)

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Record Information

Version

2.0

Created at

2022-09-10 18:00:30 UTC

Updated at

2022-09-10 18:00:31 UTC

NP-MRD ID

NP0303553

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid

Description

(3S,5R)-3-hydroxy-5-[(1S,2S,7R,10S,11R,14S,17S)-17-hydroxy-2,6,6,10,11-pentamethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-15-en-14-yl]-2,2-dimethylhexanoic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid is found in Alisma plantago-aquatica. Based on a literature review very few articles have been published on (3S,5R)-3-hydroxy-5-[(1S,2S,7R,10S,11R,14S,17S)-17-hydroxy-2,6,6,10,11-pentamethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-15-en-14-yl]-2,2-dimethylhexanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102220002D          

 35 38  0  0  1  0            999 V2000
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6095   -2.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 34 35  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102220002D          

 35 38  0  0  1  0            999 V2000
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    4.1858   -3.0277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12  2  1  1  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  6  0  0  0
 15 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 19  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 34  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0303553

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](C[C@H](O)C(C)(C)C(O)=O)[C@@H]1CC[C@@]2(C)C1=C[C@H](O)[C@H]1[C@@]3(C)CCC(=O)C(C)(C)[C@@H]3CC[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O5/c1-17(15-23(33)27(4,5)25(34)35)18-9-13-29(7)19(18)16-20(31)24-28(6)12-11-22(32)26(2,3)21(28)10-14-30(24,29)8/h16-18,20-21,23-24,31,33H,9-15H2,1-8H3,(H,34,35)/t17-,18+,20+,21+,23+,24+,28+,29+,30+/m1/s1

> <INCHI_KEY>
GVPJZRJIBZZEQZ-SZMJOBRLSA-N

> <FORMULA>
C30H48O5

> <MOLECULAR_WEIGHT>
488.709

> <EXACT_MASS>
488.350174646

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
56.54552761683671

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,5R)-3-hydroxy-5-[(1S,2S,7R,10S,11R,14S,17S)-17-hydroxy-2,6,6,10,11-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-15-en-14-yl]-2,2-dimethylhexanoic acid

> <JCHEM_LOGP>
5.382940182666669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.726454976280305

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.312999286093155

> <JCHEM_PKA_STRONGEST_BASIC>
-0.641796649688941

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
137.6843

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,5R)-3-hydroxy-5-[(1S,2S,7R,10S,11R,14S,17S)-17-hydroxy-2,6,6,10,11-pentamethyl-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-15-en-14-yl]-2,2-dimethylhexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.690  -2.668   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.109  -1.241   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.215  -2.878   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.004  -4.404   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.426  -1.353   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.741  -3.089   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -5.686  -1.873   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -5.321  -4.515   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.767  -2.755   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    2   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   34                                             
CONECT   16   15                                                            
CONECT   17   15   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   34                                                  
CONECT   22   21   23   24   31                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   22   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   21   15   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
(3S,5R)-3-Hydroxy-5-[(1S,2S,7R,10S,11R,14S,17S)-17-hydroxy-2,6,6,10,11-pentamethyl-5-oxotetracyclo[8.7.0.0,.0,]heptadec-15-en-14-yl]-2,2-dimethylhexanoate	Generator

Chemical Formula

C₃₀H₄₈O₅

Average Mass

488.7090 Da

Monoisotopic Mass

488.35017 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](C[C@H](O)C(C)(C)C(O)=O)[C@@H]1CC[C@@]2(C)C1=C[C@H](O)[C@H]1[C@@]3(C)CCC(=O)C(C)(C)[C@@H]3CC[C@]21C

InChI Identifier

InChI=1S/C30H48O5/c1-17(15-23(33)27(4,5)25(34)35)18-9-13-29(7)19(18)16-20(31)24-28(6)12-11-22(32)26(2,3)21(28)10-14-30(24,29)8/h16-18,20-21,23-24,31,33H,9-15H2,1-8H3,(H,34,35)/t17-,18+,20+,21+,23+,24+,28+,29+,30+/m1/s1

InChI Key

GVPJZRJIBZZEQZ-SZMJOBRLSA-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
Alisma plantago-aquatica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
23-hydroxysteroid
Steroid acid
3-oxosteroid
Hydroxysteroid
3-oxo-5-alpha-steroid
11-hydroxysteroid
11-beta-hydroxysteroid
Oxosteroid
Steroid
Medium-chain hydroxy acid
Medium-chain fatty acid
Beta-hydroxy acid
Branched fatty acid
Methyl-branched fatty acid
Hydroxy fatty acid
Fatty acyl
Hydroxy acid
Ketone
Secondary alcohol
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
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	5.38	ChemAxon
pKa (Strongest Acidic)	4.31	ChemAxon
pKa (Strongest Basic)	-0.64	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

163078911

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid (NP0303553)

MOL for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

3D MOL for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

3D SDF for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

3D-SDF for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

PDB for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

3D PDB for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

SMILES for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

INCHI for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

Structure for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)

3D Structure for NP0303553 ((3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid)