NP-MRD: Showing NP-Card for (1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate (NP0261251)

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Record Information

Version

2.0

Created at

2022-09-08 03:38:59 UTC

Updated at

2022-09-08 03:38:59 UTC

NP-MRD ID

NP0261251

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate

Description

Perulactone C belongs to the class of organic compounds known as tetrahydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears four hydroxyl groups. (1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate is found in Physalis peruviana. Based on a literature review very few articles have been published on Perulactone C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082205392D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309082205392D          

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    6.7859   -2.5367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0886   -1.5240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9436   -2.6817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6327   -3.4459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1391   -4.0972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9637   -4.0704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2440   -4.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5926   -5.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6194   -6.1773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9098   -4.8897    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3714   -5.5148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0962   -4.7530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  6  0  0  0
 18 20  1  6  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  6  0  0  0
 17 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 36 35  1  6  0  0  0
 13 36  1  0  0  0  0
 36 37  1  0  0  0  0
 10 37  1  0  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0261251

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@H](O)CC2=CC[C@H]3[C@@H]4CC[C@H]([C@@](C)(O)[C@H](O)C[C@@H]5COC(=O)[C@]5(C)O)[C@@]4(C)CC[C@@H]3[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O8/c1-16(31)38-25-14-19(32)12-17-6-7-20-21-8-9-23(27(21,2)11-10-22(20)28(17,25)3)30(5,36)24(33)13-18-15-37-26(34)29(18,4)35/h6,18-25,32-33,35-36H,7-15H2,1-5H3/t18-,19-,20+,21+,22+,23+,24-,25+,27+,28+,29-,30-/m1/s1

> <INCHI_KEY>
JTTNXCPQWKBGNX-PKZWWPHUSA-N

> <FORMULA>
C30H46O8

> <MOLECULAR_WEIGHT>
534.69

> <EXACT_MASS>
534.319268441

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
58.812091340671216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,5R,10S,11S,14S,15S)-14-[(2R,3R)-2,3-dihydroxy-4-[(3R,4R)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-3-yl acetate

> <JCHEM_LOGP>
1.4490597013333315

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.606953122422585

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.274770012413502

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7508940283269254

> <JCHEM_POLAR_SURFACE_AREA>
133.52

> <JCHEM_REFRACTIVITY>
140.41510000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,5R,10S,11S,14S,15S)-14-[(2R,3R)-2,3-dihydroxy-4-[(3R,4R)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-3-yl acetate

> <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       5.912  -7.062   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.388  -5.614   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.872  -5.343   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.381  -4.437   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.303  -0.998   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.366  -1.095   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.883  -3.790   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.667  -4.735   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      15.099  -2.845   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      14.828  -5.006   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      16.354  -4.795   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.248  -6.432   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      15.193  -7.648   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.732  -7.598   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      17.255  -9.047   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      16.040  -9.992   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.090 -11.531   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.765  -9.127   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.760 -10.294   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      13.246  -8.872   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.070  -4.010   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   37                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   37                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   36                                                  
CONECT   14   13   15   32                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   32                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   24   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   17   14   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   13   37                                                  
CONECT   37   36   10    5   38                                             
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₆O₈

Average Mass

534.6900 Da

Monoisotopic Mass

534.31927 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@H](O)CC2=CC[C@H]3[C@@H]4CC[C@H]([C@@](C)(O)[C@H](O)C[C@@H]5COC(=O)[C@]5(C)O)[C@@]4(C)CC[C@@H]3[C@@]12C

InChI Identifier

InChI=1S/C30H46O8/c1-16(31)38-25-14-19(32)12-17-6-7-20-21-8-9-23(27(21,2)11-10-22(20)28(17,25)3)30(5,36)24(33)13-18-15-37-26(34)29(18,4)35/h6,18-25,32-33,35-36H,7-15H2,1-5H3/t18-,19-,20+,21+,22+,23+,24-,25+,27+,28+,29-,30-/m1/s1

InChI Key

JTTNXCPQWKBGNX-PKZWWPHUSA-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
Physalis peruviana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears four hydroxyl 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

Tetrahydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Cholesterol-skeleton
Cholestane-skeleton
Tetrahydroxy bile acid, alcohol, or derivatives
25-hydroxysteroid
Steroid lactone
22-hydroxysteroid
20-hydroxysteroid
Steroid ester
3-hydroxy-delta-5-steroid
3-hydroxysteroid
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
Hydroxysteroid
Delta-5-steroid
Dicarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00056906

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

101482733

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,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate (NP0261251)

MOL for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

3D MOL for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

3D SDF for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

3D-SDF for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

PDB for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

3D PDB for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

SMILES for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

INCHI for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

Structure for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)

3D Structure for NP0261251 ((1s,3as,3bs,7r,9s,9ar,9bs,11as)-1-[(2r,3r)-2,3-dihydroxy-4-[(3r,4r)-4-hydroxy-4-methyl-5-oxooxolan-3-yl]butan-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-9-yl acetate)