NP-MRD: Showing NP-Card for 2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate (NP0175410)

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Record Information

Version

2.0

Created at

2022-09-03 12:52:18 UTC

Updated at

2022-09-03 12:52:18 UTC

NP-MRD ID

NP0175410

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate

Description

(1AS)-1abeta-Acetyloxymethyl-3beta,9beta-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5beta-ethanol acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate is found in Laurencia dendroidea. Based on a literature review very few articles have been published on (1aS)-1abeta-Acetyloxymethyl-3beta,9beta-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5beta-ethanol acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032214522D          

 36 39  0  0  1  0            999 V2000
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    2.0413   -0.7071    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.3475   -1.4732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309032214522D          

 36 39  0  0  1  0            999 V2000
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    7.2468   -2.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0426   -3.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -1.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4910   -1.0607    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9806   -1.7089    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
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 12 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
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 21 27  1  0  0  0  0
 28 27  1  1  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 11 35  1  0  0  0  0
 20 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0175410

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC[C@@]1(C)CC=C2[C@@H](C1)[C@@H](C[C@@H]1[C@@]3(COC(C)=O)C[C@H]3[C@@H](C[C@@]21C)OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O8/c1-16(29)33-10-9-26(5)8-7-21-20(12-26)23(35-18(3)31)11-25-27(21,6)14-24(36-19(4)32)22-13-28(22,25)15-34-17(2)30/h7,20,22-25H,8-15H2,1-6H3/t20-,22+,23-,24-,25+,26-,27+,28-/m1/s1

> <INCHI_KEY>
WVBOJYUDWBVSPA-RXSBWWHVSA-N

> <FORMULA>
C28H40O8

> <MOLECULAR_WEIGHT>
504.62

> <EXACT_MASS>
504.272318248

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
55.20255177804132

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1R,5S,7R,8R,10S,11S,13R,14R)-8,14-bis(acetyloxy)-11-[(acetyloxy)methyl]-1,5-dimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]ethyl acetate

> <ALOGPS_LOGP>
4.03

> <JCHEM_LOGP>
1.9877267690000002

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.396948162321494

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
130.2133

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.34e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,5S,7R,8R,10S,11S,13R,14R)-8,14-bis(acetyloxy)-11-[(acetyloxy)methyl]-1,5-dimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]ethyl acetate

> <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      -2.831  -2.298   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.522  -1.486   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.570   0.053   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.165  -2.214   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.144  -1.403   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.501  -2.131   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.811  -1.320   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.784  -0.172   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.382  -2.750   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.906  -2.970   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.859  -1.760   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.287  -0.330   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.763  -0.110   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.240   0.880   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.144   2.530   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.192   1.320   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.573   3.960   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.764   0.660   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.860  -0.990   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.080   0.534   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.870   1.487   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.090   3.011   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.520   3.583   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.880   3.964   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.384  -1.210   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.432  -2.420   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.479  -3.630   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.050  -5.060   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.575  -5.280   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.527  -4.070   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      13.146  -6.710   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.955  -3.410   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.383  -1.980   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.430  -3.190   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                                                       
CONECT    7    6    8    9   13                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   35                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12    7                                                       
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20                                                       
CONECT   20   19   21   35                                                  
CONECT   21   20   22   27   28                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21   28                                                       
CONECT   28   27   21   29                                                  
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35                                                       
CONECT   35   34   11   20   36                                             
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1AS)-1abeta-acetyloxymethyl-3b,9b-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5b-ethanol acetate	Generator
(1AS)-1abeta-acetyloxymethyl-3b,9b-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5b-ethanol acetic acid	Generator
(1AS)-1abeta-acetyloxymethyl-3beta,9beta-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5beta-ethanol acetic acid	Generator
(1AS)-1abeta-acetyloxymethyl-3β,9β-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5β-ethanol acetate	Generator
(1AS)-1abeta-acetyloxymethyl-3β,9β-bis(acetyloxy)-5,7bbeta-dimethyl-1a,1balpha,2,3,3abeta,4,5,6,7b,8,9,9abeta-dodecahydro-1H-cyclopropa[a]phenanthrene-5β-ethanol acetic acid	Generator

Chemical Formula

C₂₈H₄₀O₈

Average Mass

504.6200 Da

Monoisotopic Mass

504.27232 Da

IUPAC Name

2-[(1R,5S,7R,8R,10S,11S,13R,14R)-8,14-bis(acetyloxy)-11-[(acetyloxy)methyl]-1,5-dimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]ethyl acetate

Traditional Name

2-[(1R,5S,7R,8R,10S,11S,13R,14R)-8,14-bis(acetyloxy)-11-[(acetyloxy)methyl]-1,5-dimethyltetracyclo[8.5.0.0^{2,7}.0^{11,13}]pentadec-2-en-5-yl]ethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC[C@@]1(C)CC=C2[C@@H](C1)[C@@H](C[C@@H]1[C@@]3(COC(C)=O)C[C@H]3[C@@H](C[C@@]21C)OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C28H40O8/c1-16(29)33-10-9-26(5)8-7-21-20(12-26)23(35-18(3)31)11-25-27(21,6)14-24(36-19(4)32)22-13-28(22,25)15-34-17(2)30/h7,20,22-25H,8-15H2,1-6H3/t20-,22+,23-,24-,25+,26-,27+,28-/m1/s1

InChI Key

WVBOJYUDWBVSPA-RXSBWWHVSA-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
Laurencia dendroidea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Tetracarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.03	ALOGPS
logP	1.99	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	105.2 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	130.21 m³·mol⁻¹	ChemAxon
Polarizability	55.2 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

101588999

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate (NP0175410)

MOL for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

3D MOL for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

3D SDF for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

3D-SDF for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

PDB for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

3D PDB for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

SMILES for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

INCHI for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

Structure for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)

3D Structure for NP0175410 (2-[(1as,1bs,3r,3ar,5s,7br,9r,9ar)-3,9-bis(acetyloxy)-1a-[(acetyloxy)methyl]-5,7b-dimethyl-1h,1bh,2h,3h,3ah,4h,6h,8h,9h,9ah-cyclopropa[a]phenanthren-5-yl]ethyl acetate)