NP-MRD: Showing NP-Card for 12-Desacetylhaperforine A (NP0080973)

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Record Information

Version

2.0

Created at

2022-04-29 01:57:17 UTC

Updated at

2022-04-29 01:57:17 UTC

NP-MRD ID

NP0080973

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-Desacetylhaperforine A

Description

Methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0²,⁴.0²,⁸.0¹³,¹⁷]Heptadecan-12-yl]prop-2-enoate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 12-Desacetylhaperforine A is found in Harrisonia perforata . Based on a literature review very few articles have been published on methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0²,⁴.0²,⁸.0¹³,¹⁷]Heptadecan-12-yl]prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203572D          

 42 47  0  0  1  0            999 V2000
    1.8115   -1.4746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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 39 40  1  0  0  0  0
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 40 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292203572D          

 42 47  0  0  1  0            999 V2000
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    3.8631   -2.6827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -2.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1284   -2.0185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0709   -3.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8952   -3.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911   -0.4246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3214    0.1166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2155    0.0514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1631    0.9263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3441    1.0259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9792    1.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    1.2321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3267    0.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7841   -2.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710   -3.2016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8145   -3.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5468   -3.2378    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  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  1  0  0  0
  4 13  1  1  0  0  0
  8 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 14 18  1  0  0  0  0
  5 19  1  6  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 21 30  1  1  0  0  0
 21 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 20 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 20 37  1  1  0  0  0
  3 38  1  1  0  0  0
  1 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080973

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C/[C@@]1(C)[C@H]2[C@@H](OC(C)=O)[C@@H](O)[C@@]3(C)[C@@H](OC(=O)[C@H]4O[C@@]34[C@]2(C)[C@]2(O)OC(C)(C)C(=O)[C@]12O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H34O13/c1-13(30)39-16-17-24(4,10-8-15(31)37-7)27(35)22(34)23(2,3)42-29(27,36)26(17,6)28-20(41-28)21(33)40-19(14-9-11-38-12-14)25(28,5)18(16)32/h8-12,16-20,32,35-36H,1-7H3/b10-8-/t16-,17-,18-,19+,20-,24+,25+,26-,27+,28-,29+/m1/s1

> <INCHI_KEY>
LFADSCVXFWOCJP-MCXBSYLSSA-N

> <FORMULA>
C29H34O13

> <MOLECULAR_WEIGHT>
590.578

> <EXACT_MASS>
590.199941155

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
57.370057705788724

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0^{2,4}.0^{2,8}.0^{13,17}]heptadecan-12-yl]prop-2-enoate

> <ALOGPS_LOGP>
1.30

> <JCHEM_LOGP>
1.2166257256666673

> <ALOGPS_LOGS>
-3.07

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.734288802457877

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.23977386214516

> <JCHEM_PKA_STRONGEST_BASIC>
-2.861495605263893

> <JCHEM_POLAR_SURFACE_AREA>
191.55999999999997

> <JCHEM_REFRACTIVITY>
136.9128

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.99e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0^{2,4}.0^{2,8}.0^{13,17}]heptadecan-12-yl]prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.381  -2.753   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.543  -1.741   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.247  -0.230   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.790   0.270   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.629  -0.741   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.925  -2.253   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.397  -3.817   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.173  -0.242   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.123   1.270   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.038   2.281   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.553   3.819   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.495   1.782   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.560   1.090   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.989  -1.253   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.853  -2.787   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.270  -3.391   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.281  -2.229   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.489  -0.909   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.853  -1.942   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.593   0.519   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.721  -0.530   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.071  -1.927   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.591  -2.577   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.450  -3.558   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.211  -5.008   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.750  -5.070   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.573  -3.768   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.466  -6.433   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      11.004  -6.495   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.383  -0.793   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.067   0.218   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.736   0.096   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.771   1.729   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.242   1.915   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.295   2.445   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.621   3.181   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.371   2.300   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.343   1.740   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.330  -4.494   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.559  -5.976   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.387  -7.275   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       1.021  -6.044   0.000  0.00  0.00           C+0
CONECT    1    2    6   39                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   20   38                                             
CONECT    4    3    5   12   13                                             
CONECT    5    4    6    8   19                                             
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    4   13                                                  
CONECT   13   12    4                                                       
CONECT   14    8   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   14                                                       
CONECT   19    5                                                            
CONECT   20    3   21   34   37                                             
CONECT   21   20   22   30   31                                             
CONECT   22   21    2   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28                                                            
CONECT   30   21                                                            
CONECT   31   21   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35   36                                             
CONECT   34   33   20                                                       
CONECT   35   33                                                            
CONECT   36   33                                                            
CONECT   37   20                                                            
CONECT   38    3                                                            
CONECT   39    1   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0,.0,.0,]heptadecan-12-yl]prop-2-enoic acid	Generator

Chemical Formula

C₂₉H₃₄O₁₃

Average Mass

590.5780 Da

Monoisotopic Mass

590.19994 Da

IUPAC Name

methyl (2Z)-3-[(1R,2R,4S,7R,8S,9S,10R,11R,12S,13R,17S)-10-(acetyloxy)-7-(furan-3-yl)-9,13,17-trihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.0^{2,4}.0^{2,8}.0^{13,17}]heptadecan-12-yl]prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C/[C@@]1(C)[C@H]2[C@@H](OC(C)=O)[C@@H](O)[C@@]3(C)[C@@H](OC(=O)[C@H]4O[C@@]34[C@]2(C)[C@]2(O)OC(C)(C)C(=O)[C@]12O)C1=COC=C1

InChI Identifier

InChI=1S/C29H34O13/c1-13(30)39-16-17-24(4,10-8-15(31)37-7)27(35)22(34)23(2,3)42-29(27,36)26(17,6)28-20(41-28)21(33)40-19(14-9-11-38-12-14)25(28,5)18(16)32/h8-12,16-20,32,35-36H,1-7H3/b10-8-/t16-,17-,18-,19+,20-,24+,25+,26-,27+,28-,29+/m1/s1

InChI Key

LFADSCVXFWOCJP-MCXBSYLSSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Harrisonia perforata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Tricarboxylic acid or derivatives
Delta_valerolactone
Fatty acid ester
Dioxepane
Delta valerolactone
1,4-dioxepane
Fatty acyl
Oxane
3-furanone
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tetrahydrofuran
Tertiary alcohol
Furan
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.3	ALOGPS
logP	1.22	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	10.24	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	191.56 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	136.91 m³·mol⁻¹	ChemAxon
Polarizability	57.37 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	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

154495950

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 12-Desacetylhaperforine A (NP0080973)

MOL for NP0080973 (12-Desacetylhaperforine A)

3D MOL for NP0080973 (12-Desacetylhaperforine A)

3D SDF for NP0080973 (12-Desacetylhaperforine A)

3D-SDF for NP0080973 (12-Desacetylhaperforine A)

PDB for NP0080973 (12-Desacetylhaperforine A)

3D PDB for NP0080973 (12-Desacetylhaperforine A)

SMILES for NP0080973 (12-Desacetylhaperforine A)

INCHI for NP0080973 (12-Desacetylhaperforine A)

Structure for NP0080973 (12-Desacetylhaperforine A)

3D Structure for NP0080973 (12-Desacetylhaperforine A)