NP-MRD: Showing NP-Card for 7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate (NP0242675)

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Record Information

Version

2.0

Created at

2022-09-07 03:02:50 UTC

Updated at

2022-09-07 03:02:50 UTC

NP-MRD ID

NP0242675

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate

Description

5'-Hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]Heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-16'-yl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate is found in Cleome africana. 5'-Hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]Heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-16'-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502032D          

 38 43  0  0  0  0            999 V2000
    3.5743    2.5809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

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 38 90  1  6
M  END


  Mrv1533004181502032D          

 38 43  0  0  0  0            999 V2000
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    6.6366    0.6958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4585    0.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2876   -0.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0844   -0.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2153   -0.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4657   -0.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1166   -0.8708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2948   -0.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8219   -0.2662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4729   -1.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000   -0.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1570   -1.1476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5032   -0.9963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7232   -0.7273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    0.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8390    0.9163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804    1.4132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4208    1.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3199    0.2724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9785   -0.2244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8775   -1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2841    0.5691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814    2.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3823    3.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002    2.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4626    2.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5271    0.3383    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
  8 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
 14 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  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  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 28 33  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 26 38  1  0  0  0  0
  5 38  1  0  0  0  0
 22 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242675

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C3(C)CCC(O)C(C)(C)C3CCC2(C)C2(C)CCC3(OC4(CCC3(C)O4)C(C)(C)O)C12

> <INCHI_IDENTIFIER>
InChI=1S/C32H52O6/c1-19(33)36-20-18-22-27(6)12-11-23(34)25(2,3)21(27)10-13-28(22,7)29(8)14-16-31(24(20)29)30(9)15-17-32(37-30,38-31)26(4,5)35/h20-24,34-35H,10-18H2,1-9H3

> <INCHI_KEY>
SVYLRWXAPACCMH-UHFFFAOYSA-N

> <FORMULA>
C32H52O6

> <MOLECULAR_WEIGHT>
532.762

> <EXACT_MASS>
532.376389394

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
61.427943550295325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5'-hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-16'-yl acetate

> <ALOGPS_LOGP>
4.74

> <JCHEM_LOGP>
4.697856733666669

> <ALOGPS_LOGS>
-6.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.48943338721567

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.364970727765634

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8348952054989301

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
144.6448

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.09e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5'-hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-16'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0       6.672   4.818   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.138   4.684   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.255   5.946   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.486   3.289   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.369   2.027   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.903   2.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.786   0.898   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.320   1.032   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.437   2.294   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.971   2.427   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.506   2.561   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.388   1.299   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.923   1.432   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.737  -0.097   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.224  -0.496   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.602  -1.631   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.203  -0.230   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.551  -1.625   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.017  -1.759   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.134  -0.497   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.483  -1.892   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.600  -0.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.893  -2.142   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.673  -1.860   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.217  -1.358   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.244   0.182   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.433   1.710   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.203   2.638   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.786   2.037   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.597   0.508   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.827  -0.419   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.638  -1.947   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.397   1.062   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.392   4.166   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.580   5.695   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.920   3.978   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.863   4.355   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.717   0.632   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   38                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9   10   17                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    7   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   23   24   38                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   31   38                                             
CONECT   27   26   28                                                       
CONECT   28   27   29   33   34                                             
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   28                                                       
CONECT   34   28   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34                                                            
CONECT   38   26    5   22                                                  
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Value	Source
5'-Hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0,.0,]heptadecane]-16'-yl acetic acid	Generator
5'-Hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-16'-yl acetic acid	Generator

Chemical Formula

C₃₂H₅₂O₆

Average Mass

532.7620 Da

Monoisotopic Mass

532.37639 Da

IUPAC Name

5'-hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-16'-yl acetate

Traditional Name

5'-hydroxy-4-(2-hydroxypropan-2-yl)-1,2',6',6',10',11'-hexamethyl-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane]-16'-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C3(C)CCC(O)C(C)(C)C3CCC2(C)C2(C)CCC3(OC4(CCC3(C)O4)C(C)(C)O)C12

InChI Identifier

InChI=1S/C32H52O6/c1-19(33)36-20-18-22-27(6)12-11-23(34)25(2,3)21(27)10-13-28(22,7)29(8)14-16-31(24(20)29)30(9)15-17-32(37-30,38-31)26(4,5)35/h20-24,34-35H,10-18H2,1-9H3

InChI Key

SVYLRWXAPACCMH-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
Cleome africana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroid ester
3-hydroxysteroid
Hydroxysteroid
Steroid
Ketal
Oxane
Tetrahydrofuran
Tertiary alcohol
Meta-dioxolane
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Acetal
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Organooxygen compound
Organic oxygen 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	4.74	ALOGPS
logP	4.7	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	13.36	ChemAxon
pKa (Strongest Basic)	-0.83	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	144.64 m³·mol⁻¹	ChemAxon
Polarizability	61.43 Å³	ChemAxon
Number of Rings	6	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

85244934

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate (NP0242675)

MOL for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

3D MOL for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

3D SDF for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

3D-SDF for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

PDB for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

3D PDB for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

SMILES for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

INCHI for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

Structure for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)

3D Structure for NP0242675 (7'-hydroxy-4-(2-hydroxypropan-2-yl)-1,3'a,3'b,6',6',9'a-hexamethyl-dodecahydro-3,7-dioxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclopenta[a]phenanthren]-11'-yl acetate)