NP-MRD: Showing NP-Card for {1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate (NP0217907)

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Record Information

Version

2.0

Created at

2022-09-05 18:24:01 UTC

Updated at

2022-09-05 18:24:01 UTC

NP-MRD ID

NP0217907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate

Description

{14-[1-(4,5-Dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-4,11-dien-15-yl}methyl acetate belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring. {1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate is found in Physalis chenopodifolia. {14-[1-(4,5-Dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-4,11-dien-15-yl}methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171512332D          

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M  END

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M  END


  Mrv1533004171512332D          

 39 43  0  0  0  0            999 V2000
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    4.1731   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218   -1.2340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0683   -2.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9469   -3.3055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3074   -2.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6263   -3.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5465   -3.1272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9885   -2.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1701   -1.9432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8512   -1.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3508   -0.5257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0319    0.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1691   -0.6300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6686    0.0266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880   -1.3909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0329   -1.0780    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  9 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 10 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  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
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 31 38  1  0  0  0  0
 33 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217907

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC12CCC3C(CC(O)C4(O)CC=CC(=O)C34C)C1=CCC2(O)C(C)(O)C1CC(C)=C(C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O9/c1-16-13-24(39-25(34)17(16)2)27(5,35)30(37)12-9-21-19-14-23(33)29(36)10-6-7-22(32)26(29,4)20(19)8-11-28(21,30)15-38-18(3)31/h6-7,9,19-20,23-24,33,35-37H,8,10-15H2,1-5H3

> <INCHI_KEY>
QJTIYAVENVBOSV-UHFFFAOYSA-N

> <FORMULA>
C30H40O9

> <MOLECULAR_WEIGHT>
544.641

> <EXACT_MASS>
544.267232868

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
58.029903873968216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{14-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-4,11-dien-15-yl}methyl acetate

> <ALOGPS_LOGP>
1.72

> <JCHEM_LOGP>
1.3680280079999996

> <ALOGPS_LOGS>
-3.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.20560494143988

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.543430479886801

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2626998391046813

> <JCHEM_POLAR_SURFACE_AREA>
150.59

> <JCHEM_REFRACTIVITY>
142.24700000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.45e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{14-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-4,11-dien-15-yl}methyl acetate

> <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       7.652 -10.018   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.787  -8.743   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.251  -8.854   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.459  -7.358   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.868   0.190   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.861  -0.987   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.284  -6.510   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.501  -6.170   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.307  -5.242   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.902  -6.663   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.887  -5.838   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.712  -3.822   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.184  -3.627   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.589  -2.207   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.521  -0.981   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.926   0.439   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.049  -1.176   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.981   0.050   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       4.644  -2.596   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.061  -2.012   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                                                       
CONECT    6    5    7   23   26                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   21                                                  
CONECT   10    9   11   23                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   21                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    9   14   22                                             
CONECT   22   21                                                            
CONECT   23   10    6   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    6   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32   38                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   39                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   31                                                       
CONECT   39   33                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
{14-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0,.0,]heptadeca-4,11-dien-15-yl}methyl acetic acid	Generator
{14-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-4,11-dien-15-yl}methyl acetic acid	Generator

Chemical Formula

C₃₀H₄₀O₉

Average Mass

544.6410 Da

Monoisotopic Mass

544.26723 Da

IUPAC Name

{14-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-4,11-dien-15-yl}methyl acetate

Traditional Name

{14-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-7,8,14-trihydroxy-2-methyl-3-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-4,11-dien-15-yl}methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC12CCC3C(CC(O)C4(O)CC=CC(=O)C34C)C1=CCC2(O)C(C)(O)C1CC(C)=C(C)C(=O)O1

InChI Identifier

InChI=1S/C30H40O9/c1-16-13-24(39-25(34)17(16)2)27(5,35)30(37)12-9-21-19-14-23(33)29(36)10-6-7-22(32)26(29,4)20(19)8-11-28(21,30)15-38-18(3)31/h6-7,9,19-20,23-24,33,35-37H,8,10-15H2,1-5H3

InChI Key

QJTIYAVENVBOSV-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
Physalis chenopodiifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Withanolides and derivatives

Alternative Parents

Substituents

Withanolide-skeleton
20-hydroxysteroid
Steroid ester
6-hydroxysteroid
5-hydroxysteroid
Hydroxysteroid
1-oxosteroid
Oxosteroid
17-hydroxysteroid
Cyclohexenone
Dihydropyranone
Pyran
Dicarboxylic acid or derivatives
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Polyol
Organoheterocyclic compound
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
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
logP	1.72	ALOGPS
logP	1.37	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	12.54	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	150.59 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	142.25 m³·mol⁻¹	ChemAxon
Polarizability	58.03 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate (NP0217907)

MOL for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

3D MOL for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

3D SDF for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

3D-SDF for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

PDB for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

3D PDB for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

SMILES for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

INCHI for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

Structure for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)

3D Structure for NP0217907 ({1-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-1,5,5a-trihydroxy-9a-methyl-9-oxo-2h,3bh,4h,5h,6h,9bh,10h,11h-cyclopenta[a]phenanthren-11a-yl}methyl acetate)