NP-MRD: Showing NP-Card for (3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate (NP0335643)

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Record Information

Version

2.0

Created at

2024-09-11 02:33:27 UTC

Updated at

2024-09-11 02:33:28 UTC

NP-MRD ID

NP0335643

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate

Description

(3B,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on (3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262305052D          

 37 42  0  0  0  0            999 V2000
   -2.1574   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4429   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4429   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436    2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0305   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2242   -0.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    1.6499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4311    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4349    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9163   -2.0884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4349   -2.0884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -0.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2 34  1  0  0  0  0
  3  4  1  0  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 23  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
  9 11  1  0  0  0  0
  9 26  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 27  1  0  0  0  0
 12 13  1  0  0  0  0
 12 18  1  0  0  0  0
 12 28  1  0  0  0  0
 13 14  1  0  0  0  0
 13 29  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 32  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 30  1  0  0  0  0
 21 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END


  Mrv2104 05262305052D          

 37 42  0  0  0  0            999 V2000
   -2.1574   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1574   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4429   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4429   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0140    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290   -0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436   -0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    0.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8436    2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7285    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8554   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0305   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2242   -0.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7001    1.6499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4311    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4349    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9163   -2.0884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4349   -2.0884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -0.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2 34  1  0  0  0  0
  3  4  1  0  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 23  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
  9 11  1  0  0  0  0
  9 26  1  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 11 15  1  0  0  0  0
 11 27  1  0  0  0  0
 12 13  1  0  0  0  0
 12 18  1  0  0  0  0
 12 28  1  0  0  0  0
 13 14  1  0  0  0  0
 13 29  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 32  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 30  1  0  0  0  0
 21 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0335643

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CCC2(C)C(CCC3(C)C2CC(=O)C24OC(=O)C5(CCC(C)(C)CC25)CCC34C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1/C32H48O5/c1-19(33)36-24-10-11-28(6)20(27(24,4)5)9-12-29(7)21(28)17-23(34)32-22-18-26(2,3)13-15-31(22,25(35)37-32)16-14-30(29,32)8/h20-22,24H,9-18H2,1-8H3

> <INCHI_KEY>
CWTOUABHZIFLIH-UHFFFAOYNA-N

> <FORMULA>
C32H48O5

> <MOLECULAR_WEIGHT>
512.731

> <EXACT_MASS>
512.350174646

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
59.29455269333802

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,9,9,13,20,20-heptamethyl-16,23-dioxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosan-10-yl acetate

> <JCHEM_LOGP>
6.5132875133333314

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.827938165908282

> <JCHEM_PKA_STRONGEST_BASIC>
-6.748814425010033

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
140.42409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4,5,9,9,13,20,20-heptamethyl-16,23-dioxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosan-10-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0      -4.027  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.027  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.693  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.360  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.360  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.693  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.026  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.307  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.307  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.026  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.641  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.641   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.307   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.026   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.974  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.308  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.308   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.974   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.642   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.642   3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.308   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.974   3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.360   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.463  -5.184   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.924  -5.184   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.307   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.641  -2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.152  -0.066   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.307   3.080   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.538   5.184   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.078   5.184   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.642   0.000   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.278   0.000   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -5.444  -3.898   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -6.861  -3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -8.278  -3.898   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -6.861  -1.443   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   34                                                  
CONECT    3    2    4   24   25                                             
CONECT    4    3    5    7                                                  
CONECT    5    4    6   10   23                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   26                                             
CONECT   10    5    9   14                                                  
CONECT   11    9   12   15   27                                             
CONECT   12   11   13   18   28                                             
CONECT   13   12   14   29                                                  
CONECT   14   10   13                                                       
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   32                                             
CONECT   18   12   17   22                                                  
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30   31                                             
CONECT   22   18   21                                                       
CONECT   23    5                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    9                                                            
CONECT   27   11                                                            
CONECT   28   12   32                                                       
CONECT   29   13                                                            
CONECT   30   21                                                            
CONECT   31   21                                                            
CONECT   32   17   28   33                                                  
CONECT   33   32                                                            
CONECT   34    2   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Value	Source
(3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetic acid	Generator

Chemical Formula

C₃₂H₄₈O₅

Average Mass

512.7310 Da

Monoisotopic Mass

512.35017 Da

IUPAC Name

4,5,9,9,13,20,20-heptamethyl-16,23-dioxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosan-10-yl acetate

Traditional Name

4,5,9,9,13,20,20-heptamethyl-16,23-dioxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosan-10-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CCC2(C)C(CCC3(C)C2CC(=O)C24OC(=O)C5(CCC(C)(C)CC25)CCC34C)C1(C)C

InChI Identifier

InChI=1/C32H48O5/c1-19(33)36-24-10-11-28(6)20(27(24,4)5)9-12-29(7)21(28)17-23(34)32-22-18-26(2,3)13-15-31(22,25(35)37-32)16-14-30(29,32)8/h20-22,24H,9-18H2,1-8H3

InChI Key

CWTOUABHZIFLIH-UHFFFAOYNA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

This compound 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
Caprolactone
Oxepane
Alpha-acyloxy ketone
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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	6.51	ChemAxon
pKa (Strongest Acidic)	19.83	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	140.42 m³·mol⁻¹	ChemAxon
Polarizability	59.29 Å³	ChemAxon
Number of Rings	6	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate (NP0335643)

MOL for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

3D MOL for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

3D SDF for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

3D-SDF for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

PDB for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

3D PDB for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

SMILES for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

INCHI for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

Structure for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)

3D Structure for NP0335643 ((3b,12a,13b)-3-Hydroxy-12-oxo-28,13-oleanolide 3-acetate)