NP-MRD: Showing NP-Card for 1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione (NP0214706)

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Record Information

Version

2.0

Created at

2022-09-05 14:05:13 UTC

Updated at

2022-09-05 14:05:13 UTC

NP-MRD ID

NP0214706

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione

Description

14-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-ene-12,17-dione belongs to the class of organic compounds known as cucurbitacins. These are polycyclic compounds containing the tetracyclic cucurbitane nucleus skeleton, 19-(10->9b)-abeo-10alanost-5-ene (also known as 9b-methyl-19-nor lanosta-5-ene), with a variety of oxygenation functionalities at different positions. 14-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-ene-12,17-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191516102D          

 38 41  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004191516102D          

 38 41  0  0  0  0            999 V2000
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   -0.3035   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086   -3.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2920   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1041   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6359   -0.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1965   -2.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4643   -3.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358   -3.5281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520   -1.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4798   -1.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -0.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1995   -0.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0361   -0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 23 32  1  0  0  0  0
 19 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 12 37  1  0  0  0  0
 17 37  1  0  0  0  0
 37 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214706

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)CCC(=O)C(C)(O)C1C(O)C(=O)C2(C)C3CC=C4C(CC(O)C(O)C4(C)C)C3(C)C(=O)CC12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O8/c1-25(2,37)12-11-19(32)30(8,38)22-21(34)24(36)29(7)18-10-9-15-16(13-17(31)23(35)26(15,3)4)28(18,6)20(33)14-27(22,29)5/h9,16-18,21-23,31,34-35,37-38H,10-14H2,1-8H3

> <INCHI_KEY>
JXOVARVKBWXWKT-UHFFFAOYSA-N

> <FORMULA>
C30H46O8

> <MOLECULAR_WEIGHT>
534.69

> <EXACT_MASS>
534.319268441

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
59.315920189769784

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-12,17-dione

> <ALOGPS_LOGP>
2.45

> <JCHEM_LOGP>
1.6192324923333323

> <ALOGPS_LOGS>
-3.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.213632532511344

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.618083967816876

> <JCHEM_PKA_STRONGEST_BASIC>
-2.632720971678876

> <JCHEM_POLAR_SURFACE_AREA>
152.36

> <JCHEM_REFRACTIVITY>
142.16000000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-12,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0     -12.080   0.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.555   0.648   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.344  -0.878   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -10.765   2.173   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -9.029   0.858   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.084  -0.358   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.559  -0.147   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -5.978   1.280   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.613  -1.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.829  -2.308   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.398  -0.418   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.668  -2.579   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.096  -4.058   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.545  -4.581   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.822  -4.922   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.771  -6.461   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.606  -3.977   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.237  -5.472   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.090  -4.248   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.567  -5.696   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.949  -5.967   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.942  -4.790   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.419  -3.342   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.412  -2.164   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.928  -2.436   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.920  -1.258   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.451  -3.884   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.967  -4.155   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.458  -5.061   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.600  -6.094   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.240  -6.586   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.097  -3.071   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.896  -1.893   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.620  -1.622   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.372  -0.445   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -2.136  -1.351   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.129  -2.529   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.801  -1.143   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   37                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   37                                             
CONECT   18   17                                                            
CONECT   19   17   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   23   19   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   12   17   38                                             
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₆O₈

Average Mass

534.6900 Da

Monoisotopic Mass

534.31927 Da

IUPAC Name

14-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-12,17-dione

Traditional Name

14-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-4,5,13-trihydroxy-1,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-12,17-dione

CAS Registry Number

Not Available

SMILES

CC(C)(O)CCC(=O)C(C)(O)C1C(O)C(=O)C2(C)C3CC=C4C(CC(O)C(O)C4(C)C)C3(C)C(=O)CC12C

InChI Identifier

InChI=1S/C30H46O8/c1-25(2,37)12-11-19(32)30(8,38)22-21(34)24(36)29(7)18-10-9-15-16(13-17(31)23(35)26(15,3)4)28(18,6)20(33)14-27(22,29)5/h9,16-18,21-23,31,34-35,37-38H,10-14H2,1-8H3

InChI Key

JXOVARVKBWXWKT-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cucurbitacins. These are polycyclic compounds containing the tetracyclic cucurbitane nucleus skeleton, 19-(10->9b)-abeo-10alanost-5-ene (also known as 9b-methyl-19-nor lanosta-5-ene), with a variety of oxygenation functionalities at different positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cucurbitacins

Direct Parent

Cucurbitacins

Alternative Parents

Substituents

Triterpenoid
Cucurbitacin skeleton
25-hydroxysteroid
22-oxosteroid
21-oxosteroid
20-hydroxysteroid
3-hydroxy-delta-5-steroid
3-hydroxysteroid
16-hydroxysteroid
2-hydroxysteroid
Oxosteroid
15-oxosteroid
11-oxosteroid
Hydroxysteroid
Delta-5-steroid
Acyloin
Cyclic alcohol
Alpha-hydroxy ketone
Tertiary alcohol
Secondary alcohol
Ketone
Polyol
Carbonyl group
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	2.45	ALOGPS
logP	1.62	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	12.62	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	152.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	142.16 m³·mol⁻¹	ChemAxon
Polarizability	59.32 Å³	ChemAxon
Number of Rings	4	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

74346959

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione (NP0214706)

MOL for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

3D MOL for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

3D SDF for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

3D-SDF for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

PDB for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

3D PDB for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

SMILES for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

INCHI for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

Structure for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)

3D Structure for NP0214706 (1-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8-trihydroxy-3a,6,6,9b,11a-pentamethyl-1h,2h,3bh,4h,7h,8h,9h,9ah,11h-cyclopenta[a]phenanthrene-3,10-dione)