NP-MRD: Showing NP-Card for 6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid (NP0209279)

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Record Information

Version

2.0

Created at

2022-09-05 06:37:34 UTC

Updated at

2022-09-05 06:37:34 UTC

NP-MRD ID

NP0209279

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid

Description

6-{10,12-Dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups. 6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid is found in Ganoderma applanatum. 6-{10,12-Dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171516022D          

 39 42  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171516022D          

 39 42  0  0  0  0            999 V2000
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    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  0  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
    2.5903   -4.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7351   -0.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5523   -0.3521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4242    0.5249    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  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  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 14 35  1  0  0  0  0
 21 35  1  0  0  0  0
 35 36  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209279

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC(=O)CC(C)(O)C1=CC(O)C2(C)C1(C)C(=O)C=C1C3(C)CCC(=O)C(C)(C)C3CC(=O)C21O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O9/c1-15(24(36)37)10-16(31)14-27(5,38)19-13-22(34)29(7)28(19,6)21(33)12-18-26(4)9-8-20(32)25(2,3)17(26)11-23(35)30(18,29)39/h12-13,15,17,22,34,38-39H,8-11,14H2,1-7H3,(H,36,37)

> <INCHI_KEY>
KSROOTXYLRZSJU-UHFFFAOYSA-N

> <FORMULA>
C30H40O9

> <MOLECULAR_WEIGHT>
544.641

> <EXACT_MASS>
544.267232868

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
57.26950109204812

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid

> <ALOGPS_LOGP>
2.06

> <JCHEM_LOGP>
2.0918096796666674

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.998909415677083

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.0071432936603335

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1390416005063653

> <JCHEM_POLAR_SURFACE_AREA>
166.26999999999995

> <JCHEM_REFRACTIVITY>
141.7175

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -4.741  -3.089   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.160  -1.662   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.635  -1.452   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      -2.270  -4.094   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.164  -2.457   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.997  -2.728   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.435  -4.618   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.623  -8.771   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.594  -3.453   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  O   UNK     0       3.735  -2.213   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+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  O   UNK     0       4.835  -9.184   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       4.724  -7.984   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -5.105  -0.447   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -6.631  -0.657   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -4.525   0.980   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   35                                             
CONECT   15   14                                                            
CONECT   16   14   10   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   35                                                  
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   35                                                  
CONECT   34   33                                                            
CONECT   35   33   14   21   36                                             
CONECT   36   35                                                            
CONECT   37    2   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Value	Source
6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0,.0,]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoate	Generator
6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoate	Generator

Chemical Formula

C₃₀H₄₀O₉

Average Mass

544.6410 Da

Monoisotopic Mass

544.26723 Da

IUPAC Name

6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid

Traditional Name

6-{10,12-dihydroxy-2,6,6,11,15-pentamethyl-5,9,16-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),13-dien-14-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid

CAS Registry Number

Not Available

SMILES

CC(CC(=O)CC(C)(O)C1=CC(O)C2(C)C1(C)C(=O)C=C1C3(C)CCC(=O)C(C)(C)C3CC(=O)C21O)C(O)=O

InChI Identifier

InChI=1S/C30H40O9/c1-15(24(36)37)10-16(31)14-27(5,38)19-13-22(34)29(7)28(19,6)21(33)12-18-26(4)9-8-20(32)25(2,3)17(26)11-23(35)30(18,29)39/h12-13,15,17,22,34,38-39H,8-11,14H2,1-7H3,(H,36,37)

InChI Key

KSROOTXYLRZSJU-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

Species Name	Source	Reference
Ganoderma applanatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Dihydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Dihydroxy bile acid, alcohol, or derivatives
23-oxosteroid
20-hydroxysteroid
Steroid acid
3-oxosteroid
7-oxosteroid
15-hydroxysteroid
Oxosteroid
12-oxosteroid
Hydroxysteroid
Medium-chain keto acid
Gamma-keto acid
Cyclohexenone
Beta-hydroxy ketone
Keto acid
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Cyclic ketone
Ketone
Carboxylic acid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
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	2.06	ALOGPS
logP	2.09	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	4.01	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	166.27 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	141.72 m³·mol⁻¹	ChemAxon
Polarizability	57.27 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

73197792

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid (NP0209279)

MOL for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

3D MOL for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

3D SDF for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

3D-SDF for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

PDB for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

3D PDB for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

SMILES for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

INCHI for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

Structure for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)

3D Structure for NP0209279 (6-{3,3b-dihydroxy-3a,6,6,9a,11a-pentamethyl-4,7,11-trioxo-3h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-1-yl}-6-hydroxy-2-methyl-4-oxoheptanoic acid)