NP-MRD: Showing NP-Card for (1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate (NP0147497)

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Record Information

Version

2.0

Created at

2022-09-02 03:06:53 UTC

Updated at

2022-09-02 03:06:54 UTC

NP-MRD ID

NP0147497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate

Description

Taxusecone belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate is found in Taxus cuspidata. (1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate was first documented in 2009 (PMID: 19270408). Based on a literature review very few articles have been published on Taxusecone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205062D          

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M  END

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M  END


  Mrv1652309022205062D          

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    4.4643   -0.5696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4989   -1.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1146   -2.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1187   -2.2937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4344   -3.0559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -3.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7546   -2.5091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5681   -3.9258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3860   -4.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0658   -4.5803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2937   -2.2937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9780   -3.0559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4802   -3.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1645   -4.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2982   -3.6027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7103   -1.7103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  1  0  0  0
 28 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 35 40  1  0  0  0  0
 40  2  1  6  0  0  0
 11 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147497

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](O)C(=O)C[C@H]1[C@@H](OC(C)=O)[C@@H]2C(=C)[C@@H](O)C[C@H](OC(C)=O)[C@@]2(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C(=O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O12/c1-12-19(34)11-21(37-14(3)30)28(9)22(12)23(38-15(4)31)18(10-20(35)13(2)29)27(7,8)25(36)24(39-16(5)32)26(28)40-17(6)33/h13,18-19,21-24,26,29,34H,1,10-11H2,2-9H3/t13-,18+,19+,21+,22+,23-,24-,26+,28-/m1/s1

> <INCHI_KEY>
JKJCHWRPJSEJKT-MUAKEAJSSA-N

> <FORMULA>
C28H40O12

> <MOLECULAR_WEIGHT>
568.616

> <EXACT_MASS>
568.251976728

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
57.21518674861639

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,4aR,5R,6R,9S,10R,10aS)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3R)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-dodecahydrobenzo[8]annulen-1-yl acetate

> <ALOGPS_LOGP>
0.67

> <JCHEM_LOGP>
0.41690228233333354

> <ALOGPS_LOGS>
-3.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.401603434268601

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.61880381277927

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0025124436911277

> <JCHEM_POLAR_SURFACE_AREA>
179.79999999999998

> <JCHEM_REFRACTIVITY>
136.1939

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.62e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4aR,5R,6R,9S,10R,10aS)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3R)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.859  -5.503   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.859  -3.963   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.525  -3.193   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.808  -3.963   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.525  -1.653   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.859  -0.883   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.859   0.657   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.525   1.427   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.525   2.967   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.808   0.657   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.193  -1.653   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.992  -0.126   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.282  -0.564   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.692   0.859   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.630   2.081   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.040   3.504   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.157   1.880   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.822  -0.564   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.411   0.859   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.938   1.060   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.527   2.483   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.875  -0.162   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.911  -1.653   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.333  -1.063   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.911  -3.193   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.398  -2.794   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.681  -4.526   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.822  -4.282   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.411  -5.704   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.938  -5.905   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.875  -4.684   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.527  -7.328   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.054  -7.529   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.590  -8.550   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.282  -4.282   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.692  -5.704   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.630  -6.926   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.040  -8.349   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.157  -6.725   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.193  -3.193   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   40                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   40                                             
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   28   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   35    2   11                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₄₀O₁₂

Average Mass

568.6160 Da

Monoisotopic Mass

568.25198 Da

IUPAC Name

(1S,3S,4aR,5R,6R,9S,10R,10aS)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3R)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-dodecahydrobenzo[8]annulen-1-yl acetate

Traditional Name

(1S,3S,4aR,5R,6R,9S,10R,10aS)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3R)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H](O)C(=O)C[C@H]1[C@@H](OC(C)=O)[C@@H]2C(=C)[C@@H](O)C[C@H](OC(C)=O)[C@@]2(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C(=O)C1(C)C

InChI Identifier

InChI=1S/C28H40O12/c1-12-19(34)11-21(37-14(3)30)28(9)22(12)23(38-15(4)31)18(10-20(35)13(2)29)27(7,8)25(36)24(39-16(5)32)26(28)40-17(6)33/h13,18-19,21-24,26,29,34H,1,10-11H2,2-9H3/t13-,18+,19+,21+,22+,23-,24-,26+,28-/m1/s1

InChI Key

JKJCHWRPJSEJKT-MUAKEAJSSA-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
Taxus cuspidata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Alpha-acyloxy ketone
Acyloin
Alpha-hydroxy ketone
Cyclic alcohol
Carboxylic acid ester
Cyclic ketone
Secondary alcohol
Ketone
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alcohol
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	0.67	ALOGPS
logP	0.42	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	179.8 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	136.19 m³·mol⁻¹	ChemAxon
Polarizability	57.22 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	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

102285370

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yu SH, Ni ZY, Zhang J, Dong M, Sauriol F, Huo CH, Shi QW, Gu YC, Kiyota H, Cong B: Taxusecone, a novel taxane with an unprecedented 11,12-secotaxane skeleton, from Taxus cuspidata needles. Biosci Biotechnol Biochem. 2009 Mar 23;73(3):756-8. doi: 10.1271/bbb.80698. Epub 2009 Mar 7. [PubMed:19270408 ]
LOTUS database [Link]

Showing NP-Card for (1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate (NP0147497)

MOL for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

3D MOL for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

3D SDF for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

3D-SDF for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

PDB for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

3D PDB for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

SMILES for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

INCHI for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

Structure for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)

3D Structure for NP0147497 ((1s,3s,4ar,5r,6r,9s,10r,10as)-5,9,10-tris(acetyloxy)-3-hydroxy-6-[(3r)-3-hydroxy-2-oxobutyl]-7,7,10a-trimethyl-4-methylidene-8-oxo-octahydrobenzo[8]annulen-1-yl acetate)