NP-MRD: Showing NP-Card for Thapsigargicin (NP0063817)

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Record Information

Version

1.0

Created at

2022-04-28 08:09:38 UTC

Updated at

2022-04-28 08:09:38 UTC

NP-MRD ID

NP0063817

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Thapsigargicin

Description

Thapsigargicin belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. Thapsigargicin is found in Thapsia garganica. It was first documented in 2009 (PMID: 20017396). Based on a literature review a significant number of articles have been published on thapsigargicin (PMID: 35483916) (PMID: 35483915) (PMID: 35483914) (PMID: 19914344).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282210092D          

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M  END

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M  END


  Mrv1652304282210092D          

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    0.7597   -0.6886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4742   -1.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4159   -1.8380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1365   -2.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8999   -1.9269    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1312   -1.1350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6563   -0.4604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1512    0.1997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9319   -0.0669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6065    0.4080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9196   -0.8918    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.7376   -0.9989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2517   -1.6470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7189   -1.7140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5130   -2.4789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3414   -3.2859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9545   -3.8379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5568   -3.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3853   -4.3478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6007   -4.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -2.5674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5992   -1.9548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2921   -2.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4754   -2.8374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8016   -3.3694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7559    1.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0002    0.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1718    1.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9564    1.7458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5587    2.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7302    2.8499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5148    3.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7741    1.7880    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  1  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  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
  3 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 17 25  1  1  0  0  0
 16 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 32  1  6  0  0  0
 14 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
  2 37  1  0  0  0  0
  1 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0063817

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(=O)O[C@@H]1[C@@H](OC(=O)C(\C)=C/C)C(C)=C2[C@@H]3OC(=O)[C@@](C)(O)[C@@]3(O)[C@H](C[C@](C)(OC(C)=O)[C@@H]12)OC(=O)CCC

> <INCHI_IDENTIFIER>
InChI=1S/C32H46O12/c1-9-12-13-15-22(35)41-26-24-23(18(5)25(26)42-28(36)17(4)11-3)27-32(39,31(8,38)29(37)43-27)20(40-21(34)14-10-2)16-30(24,7)44-19(6)33/h11,20,24-27,38-39H,9-10,12-16H2,1-8H3/b17-11-/t20-,24+,25-,26-,27-,30-,31+,32+/m0/s1

> <INCHI_KEY>
LXWLOFYIORKNSA-FFOGNQQCSA-N

> <FORMULA>
C32H46O12

> <MOLECULAR_WEIGHT>
622.708

> <EXACT_MASS>
622.298926921

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
66.63115384617873

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,3aR,4S,6S,6aR,7S,8S,9bS)-6-(acetyloxy)-4-(butanoyloxy)-3,3a-dihydroxy-3,6,9-trimethyl-8-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-7-yl hexanoate

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
3.4953881656666645

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.498704796841494

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.135565750741481

> <JCHEM_PKA_STRONGEST_BASIC>
-4.307623186172571

> <JCHEM_POLAR_SURFACE_AREA>
171.95999999999998

> <JCHEM_REFRACTIVITY>
154.61380000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3aR,4S,6S,6aR,7S,8S,9bS)-6-(acetyloxy)-4-(butanoyloxy)-3,3a-dihydroxy-3,6,9-trimethyl-8-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-4H,5H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-7-yl hexanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -6.745   0.246   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.251   0.566   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.021  -0.767   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.991  -1.912   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.584  -1.285   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.250  -2.055   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -3.917  -1.285   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.917   0.255   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.583  -2.055   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.249  -1.285   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.084  -2.055   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.418  -1.285   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.752  -2.055   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.243  -3.431   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.588  -4.181   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -11.013  -3.597   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -11.445  -2.119   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -10.558  -0.859   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0     -11.482   0.373   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0     -12.940  -0.125   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -14.199   0.762   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -12.917  -1.665   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -14.443  -1.865   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0     -13.537  -3.074   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0     -12.542  -3.199   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0     -12.158  -4.627   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -11.837  -6.134   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -12.982  -7.164   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -10.373  -6.610   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -10.053  -8.116   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.588  -8.592   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -7.523  -4.792   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -6.719  -3.649   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -6.145  -5.078   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -4.621  -5.296   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -7.096  -6.290   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -8.878   1.973   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -5.600   1.277   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -5.921   2.783   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -7.385   3.259   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -4.776   3.813   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -5.096   5.320   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -6.561   5.796   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -3.312   3.338   0.000  0.00  0.00           C+0
CONECT    1    2    5   38                                                  
CONECT    2    1    3   37                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    4   15   32   33                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   22   25                                             
CONECT   18   17    3   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   17   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   17                                                            
CONECT   26   16   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   14                                                            
CONECT   33   14   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37    2                                                            
CONECT   38    1   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₆O₁₂

Average Mass

622.7080 Da

Monoisotopic Mass

622.29893 Da

IUPAC Name

(3S,3aR,4S,6S,6aR,7S,8S,9bS)-6-(acetyloxy)-4-(butanoyloxy)-3,3a-dihydroxy-3,6,9-trimethyl-8-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-7-yl hexanoate

Traditional Name

(3S,3aR,4S,6S,6aR,7S,8S,9bS)-6-(acetyloxy)-4-(butanoyloxy)-3,3a-dihydroxy-3,6,9-trimethyl-8-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-4H,5H,6aH,7H,8H,9bH-azuleno[4,5-b]furan-7-yl hexanoate

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)O[C@@H]1[C@@H](OC(=O)C(\C)=C/C)C(C)=C2[C@@H]3OC(=O)[C@@](C)(O)[C@@]3(O)[C@H](C[C@](C)(OC(C)=O)[C@@H]12)OC(=O)CCC

InChI Identifier

InChI=1S/C32H46O12/c1-9-12-13-15-22(35)41-26-24-23(18(5)25(26)42-28(36)17(4)11-3)27-32(39,31(8,38)29(37)43-27)20(40-21(34)14-10-2)16-30(24,7)44-19(6)33/h11,20,24-27,38-39H,9-10,12-16H2,1-8H3/b17-11-/t20-,24+,25-,26-,27-,30-,31+,32+/m0/s1

InChI Key

LXWLOFYIORKNSA-FFOGNQQCSA-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
Thapsia garganica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Fatty acid ester
Gamma butyrolactone
Fatty acyl
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
1,2-diol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.18	ALOGPS
logP	3.5	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	11.14	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	171.96 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	154.61 m³·mol⁻¹	ChemAxon
Polarizability	66.63 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	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

C00020715

Chemspider ID

8433846

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10258363

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

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Oztetik E: [Effects of thapsigargicin on Ca2+ movements in L1210 cells permeabilized with digitonin]. Biomed Khim. 2009 Sep-Oct;55(5):651-62. [PubMed:20017396 ]
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Showing NP-Card for Thapsigargicin (NP0063817)

MOL for NP0063817 (Thapsigargicin)

3D MOL for NP0063817 (Thapsigargicin)

3D SDF for NP0063817 (Thapsigargicin)

3D-SDF for NP0063817 (Thapsigargicin)

PDB for NP0063817 (Thapsigargicin)

3D PDB for NP0063817 (Thapsigargicin)

SMILES for NP0063817 (Thapsigargicin)

INCHI for NP0063817 (Thapsigargicin)

Structure for NP0063817 (Thapsigargicin)

3D Structure for NP0063817 (Thapsigargicin)