NP-MRD: Showing NP-Card for (1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one (NP0281960)

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Record Information

Version

2.0

Created at

2022-09-09 08:36:25 UTC

Updated at

2022-09-09 08:36:26 UTC

NP-MRD ID

NP0281960

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one

Description

(1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0¹,¹³.0⁴,⁹]Hexadecan-2-one belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. (1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one is found in Huperzia chinensis and Huperzia serrata. Based on a literature review very few articles have been published on (1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0¹,¹³.0⁴,⁹]Hexadecan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 48  0  0  0  0  0  0  0  0999 V2000
    3.8246   -0.4347   -1.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9789   -0.1079    0.0845 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1346   -1.2793    0.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8061   -0.7758    0.9224 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1042   -1.7869    1.5137 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1051   -0.1104   -0.2257 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2413   -1.0466   -1.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2198   -2.0563   -0.8378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2615   -1.6305    0.0960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9975   -0.4935    0.9222 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2622    0.2423    1.0990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3527    1.2208   -0.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1296    0.8505   -0.8924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2170    0.4453    0.2143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8168    1.6543    0.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1267    2.0863    2.0348 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1511    2.3065   -0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8694    1.1069   -0.6071 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2771    1.1684   -0.1057 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0055    1.9327   -1.0506 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3437   -0.0454   -2.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    0.0587   -1.0914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0335   -1.5256   -1.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7518   -0.0034    0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5670   -1.8655    1.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0925   -2.0027   -0.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866    0.0107    1.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6035   -2.6357    1.6189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6036   -0.4454   -2.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423   -1.6111   -1.7346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7155   -2.4969   -1.7543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.9274   -0.4209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2531   -1.5043   -0.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4824   -2.4901    0.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1319    0.7712    2.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1273   -0.4377    1.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2856    1.1319   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1591    2.2435    0.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7933    1.6644   -1.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4728    0.0233   -1.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3691    2.9128   -0.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8014    2.9626    0.5671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8351    1.2313   -1.7031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3481    1.7625    0.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5633    1.9261   -1.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  6
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19  2  1  0
 14  6  1  0
 18  6  1  0
 14 10  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  1
  3 25  1  0
  3 26  1  0
  4 27  1  1
  5 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  6
 19 44  1  1
 20 45  1  0
M  END


  Mrv1652309092210362D          

 20 23  0  0  1  0            999 V2000
    3.2984    0.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.2102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1365   -0.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3797   -0.5242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9747   -1.3730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8352    0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1655   -0.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6760   -1.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1439   -1.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4742   -0.5230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2571   -0.2626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2513    0.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4650    0.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0153    0.1410    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1506    0.9492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9019    1.2900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5667    1.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1760    0.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9970    0.8810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3378    1.6323    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  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
 13 14  1  0  0  0  0
 14 10  1  1  0  0  0
  6 14  1  0  0  0  0
 14 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
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0281960

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C[C@H](O)C23CCCN4CCC[C@]24C(=O)CC3[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H25NO3/c1-10-8-12(18)15-4-2-6-17-7-3-5-16(15,17)13(19)9-11(15)14(10)20/h10-12,14,18,20H,2-9H2,1H3/t10?,11?,12-,14+,15?,16-/m0/s1

> <INCHI_KEY>
XPIVPCYGYLMOCY-LHXUHSBRSA-N

> <FORMULA>
C16H25NO3

> <MOLECULAR_WEIGHT>
279.38

> <EXACT_MASS>
279.183443669

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
30.691458020244312

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0^{1,13}.0^{4,9}]hexadecan-2-one

> <JCHEM_LOGP>
0.6148985556666657

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.924682847361495

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.22799045667967

> <JCHEM_PKA_STRONGEST_BASIC>
8.56314678629927

> <JCHEM_POLAR_SURFACE_AREA>
60.769999999999996

> <JCHEM_REFRACTIVITY>
75.63820000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0^{1,13}.0^{4,9}]hexadecan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.157   0.543   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.624   0.392   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.988  -1.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.575  -0.979   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.819  -2.563   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.559   0.092   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.176  -1.319   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.262  -2.559   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.269  -2.387   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.885  -0.976   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -2.347  -0.490   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.336   1.050   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.868   1.515   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.029   0.263   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.281   1.772   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.684   2.408   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.058   2.533   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.195   1.494   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.728   1.645   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.364   3.047   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   14   18                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   10    6   15                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18    2   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₅NO₃

Average Mass

279.3800 Da

Monoisotopic Mass

279.18344 Da

IUPAC Name

(1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0^{1,13}.0^{4,9}]hexadecan-2-one

Traditional Name

(1R,5R,8S)-5,8-dihydroxy-6-methyl-13-azatetracyclo[7.7.0.0^{1,13}.0^{4,9}]hexadecan-2-one

CAS Registry Number

Not Available

SMILES

CC1C[C@H](O)C23CCCN4CCC[C@]24C(=O)CC3[C@@H]1O

InChI Identifier

InChI=1S/C16H25NO3/c1-10-8-12(18)15-4-2-6-17-7-3-5-16(15,17)13(19)9-11(15)14(10)20/h10-12,14,18,20H,2-9H2,1H3/t10?,11?,12-,14+,15?,16-/m0/s1

InChI Key

XPIVPCYGYLMOCY-LHXUHSBRSA-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
Huperzia chinensis	LOTUS Database	35616633
Huperzia serrata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Azaspirodecane
Indolizidine
N-alkylpyrrolidine
Piperidine
Pyrrolidine
Cyclic alcohol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	0.61	ChemAxon
pKa (Strongest Acidic)	14.23	ChemAxon
pKa (Strongest Basic)	8.56	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	60.77 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	75.64 m³·mol⁻¹	ChemAxon
Polarizability	30.69 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

4885186

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

6326010

PDB ID

Not Available

ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one (NP0281960)

MOL for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

3D MOL for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

3D SDF for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

3D-SDF for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

PDB for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

3D PDB for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

SMILES for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

INCHI for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

Structure for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)

3D Structure for NP0281960 ((1r,4s,11ar)-1,4-dihydroxy-2-methyl-dodecahydroindeno[3a,3-i]indolizin-12-one)