NP-MRD: Showing NP-Card for (1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one (NP0169995)

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Record Information

Version

2.0

Created at

2022-09-03 06:03:01 UTC

Updated at

2022-09-03 06:03:01 UTC

NP-MRD ID

NP0169995

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one

Description

Cilistol d belongs to the class of organic compounds known as pregnane steroids. These are steroids with a structure based on the 21-carbon pregnane skeleton. (1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one is found in Solanum capsicoides. Based on a literature review very few articles have been published on Cilistol d.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032208032D          

 34 39  0  0  1  0            999 V2000
    5.6144   -2.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3289   -3.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7578   -5.5020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7578   -6.3270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4723   -5.0895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   11.4003   -2.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2019   -5.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3 33  1  0  0  0  0
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 33 34  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032208032D          

 34 39  0  0  1  0            999 V2000
    5.6144   -2.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  6  0  0  0
  8  6  1  1  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 12 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  1  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0169995

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1O[C@H](C[C@]2(C)O[C@@]12C)[C@@H](C)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4CC=CC(=O)[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O5/c1-17(22-16-26(3)28(5,34-26)24(32-6)33-22)29(31)15-13-20-19-11-10-18-8-7-9-23(30)27(18,4)21(19)12-14-25(20,29)2/h7,9-10,17,19-22,24,31H,8,11-16H2,1-6H3/t17-,19+,20+,21+,22-,24-,25+,26+,27+,28+,29+/m1/s1

> <INCHI_KEY>
JLPRPCIHUJESQL-UPDDYATBSA-N

> <FORMULA>
C29H42O5

> <MOLECULAR_WEIGHT>
470.65

> <EXACT_MASS>
470.303224452

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
53.93339466356483

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,10S,11S,14S,15S)-14-hydroxy-14-[(1R)-1-[(1R,2R,4R,6S)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7-dien-3-one

> <ALOGPS_LOGP>
5.19

> <JCHEM_LOGP>
4.6208039613333325

> <ALOGPS_LOGS>
-5.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.05086968790526

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.110898586992867

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1876907768260194

> <JCHEM_POLAR_SURFACE_AREA>
68.28999999999999

> <JCHEM_REFRACTIVITY>
131.85209999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.57e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,10S,11S,14S,15S)-14-hydroxy-14-[(1R)-1-[(1R,2R,4R,6S)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7-dien-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.480  -4.880   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.814  -5.650   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.814  -7.190   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      13.148  -7.960   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      13.148  -9.500   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.481 -10.270   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.481 -11.810   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.815  -9.500   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      16.441 -10.907   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      14.910  -8.255   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.815  -7.009   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.280  -7.485   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.613  -6.715   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.613  -5.175   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.947  -4.405   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.281  -5.175   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.614  -4.405   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.948  -5.175   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      23.948  -6.715   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.614  -7.485   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      22.614  -9.025   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      21.281  -6.715   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.281  -8.255   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.947  -7.485   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.947  -9.025   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      18.613  -9.795   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.280  -9.025   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.119 -10.556   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.814 -10.270   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.480  -9.500   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.710 -10.834   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.147  -8.730   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.480  -7.960   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.710  -6.627   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   27                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   27                                                  
CONECT   13   12   14   24                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   16   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   13   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   12    8   28                                             
CONECT   28   27                                                            
CONECT   29    5   30                                                       
CONECT   30   29   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32    3   30   34                                             
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₂O₅

Average Mass

470.6500 Da

Monoisotopic Mass

470.30322 Da

IUPAC Name

(1S,2R,10S,11S,14S,15S)-14-hydroxy-14-[(1R)-1-[(1R,2R,4R,6S)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7-dien-3-one

Traditional Name

(1S,2R,10S,11S,14S,15S)-14-hydroxy-14-[(1R)-1-[(1R,2R,4R,6S)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7-dien-3-one

CAS Registry Number

Not Available

SMILES

CO[C@@H]1O[C@H](C[C@]2(C)O[C@@]12C)[C@@H](C)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4CC=CC(=O)[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C29H42O5/c1-17(22-16-26(3)28(5,34-26)24(32-6)33-22)29(31)15-13-20-19-11-10-18-8-7-9-23(30)27(18,4)21(19)12-14-25(20,29)2/h7,9-10,17,19-22,24,31H,8,11-16H2,1-6H3/t17-,19+,20+,21+,22-,24-,25+,26+,27+,28+,29+/m1/s1

InChI Key

JLPRPCIHUJESQL-UPDDYATBSA-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
Solanum capsicoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pregnane steroids. These are steroids with a structure based on the 21-carbon pregnane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Pregnane steroids

Direct Parent

Pregnane steroids

Alternative Parents

Substituents

Pregnane-skeleton
17-hydroxysteroid
Oxosteroid
1-oxosteroid
Hydroxysteroid
Cyclohexenone
Dioxepane
1,4-dioxepane
Oxane
Tertiary alcohol
Cyclic alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	5.19	ALOGPS
logP	4.62	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	14.11	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	131.85 m³·mol⁻¹	ChemAxon
Polarizability	53.93 Å³	ChemAxon
Number of Rings	6	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

101114279

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one (NP0169995)

MOL for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D MOL for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D SDF for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D-SDF for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

PDB for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D PDB for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

SMILES for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

INCHI for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

Structure for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D Structure for NP0169995 ((1s,3as,3bs,9ar,9bs,11as)-1-hydroxy-1-[(1r)-1-[(1r,2r,4r,6s)-2-methoxy-1,6-dimethyl-3,7-dioxabicyclo[4.1.0]heptan-4-yl]ethyl]-9a,11a-dimethyl-2h,3h,3ah,3bh,4h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)