NP-MRD: Showing NP-Card for Tryprostatin B (NP0023194)

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Record Information

Version

2.0

Created at

2021-01-06 08:18:33 UTC

Updated at

2021-07-15 17:41:05 UTC

NP-MRD ID

NP0023194

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tryprostatin B

Provided By

NPAtlas

Description

Tryprostatin b is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Tryprostatin B is found in Aspergillus, Neosartorya fischeri, Aspergillus fumigatus, Cordyceps tenuipes and Isaria tenuipes BCC12625. Tryprostatin B was first documented in 2000 (PMID: 10780915). Based on a literature review a small amount of articles have been published on tryprostatin b (PMID: 12946134) (PMID: 17047877).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105403D          

 51 54  0  0  0  0            999 V2000
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   -3.8518    1.8680   -0.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5590   -1.4236    1.3096 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1819   -2.6822    1.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242105403D          

 51 54  0  0  0  0            999 V2000
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    3.8535    3.1757   -0.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3811    1.7212    0.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1446    2.8293   -0.9629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8154    0.0111   -0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    1.1451   -2.0930 H   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  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  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  2  0  0  0  0
 14  6  2  0  0  0  0
 25 16  1  0  0  0  0
 13  8  1  0  0  0  0
 24 20  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  3 32  1  0  0  0  0
  4 33  1  0  0  0  0
  5 34  1  0  0  0  0
  5 35  1  0  0  0  0
  7 36  1  0  0  0  0
  9 37  1  0  0  0  0
 10 38  1  0  0  0  0
 11 39  1  0  0  0  0
 12 40  1  0  0  0  0
 15 41  1  0  0  0  0
 15 42  1  0  0  0  0
 16 43  1  1  0  0  0
 17 44  1  0  0  0  0
 20 45  1  1  0  0  0
 21 46  1  0  0  0  0
 21 47  1  0  0  0  0
 22 48  1  0  0  0  0
 22 49  1  0  0  0  0
 23 50  1  0  0  0  0
 23 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0023194

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N1C2=C([H])C([H])=C([H])C([H])=C2C(=C1C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])[C@]1([H])N([H])C(=O)[C@@]2([H])N(C1=O)C([H])([H])C([H])([H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H25N3O2/c1-13(2)9-10-17-15(14-6-3-4-7-16(14)22-17)12-18-21(26)24-11-5-8-19(24)20(25)23-18/h3-4,6-7,9,18-19,22H,5,8,10-12H2,1-2H3,(H,23,25)/t18-,19-/m0/s1

> <INCHI_KEY>
GLWYBXPXOSKQAW-OALUTQOASA-N

> <FORMULA>
C21H25N3O2

> <MOLECULAR_WEIGHT>
351.45

> <EXACT_MASS>
351.194677057

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.038571839163076

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,8aS)-3-{[2-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-octahydropyrrolo[1,2-a]pyrazine-1,4-dione

> <ALOGPS_LOGP>
2.87

> <JCHEM_LOGP>
2.4473766066666673

> <ALOGPS_LOGS>
-3.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.63562795054267

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.512815034120264

> <JCHEM_PKA_STRONGEST_BASIC>
-4.044497661720303

> <JCHEM_POLAR_SURFACE_AREA>
65.2

> <JCHEM_REFRACTIVITY>
102.26369999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,8aS)-3-{[2-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -4.5948    2.0830    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8518    1.8680   -0.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4708    2.2460   -1.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6546    1.3438   -0.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9756    0.9360    0.8182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7398   -0.5203    0.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5590   -1.4236    1.3096 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1819   -2.6822    1.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6972   -3.9067    1.4035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0519   -5.0314    0.9350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9368   -4.9540    0.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4577   -3.7212   -0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681   -2.5612    0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7815   -1.2170    0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3747   -0.7191   -0.7281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6277   -0.5029    0.0703 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4453    0.4311    1.1446 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3924    1.4846    1.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427    2.5420    1.8357 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806    1.3477    0.7951 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4318    2.6556    0.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6787    2.1064   -0.2996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299    0.8778   -1.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8264    0.6417   -0.4638 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6959   -0.0788   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424   -0.3991   -2.1259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6362    2.4319    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7028    1.0612    1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    2.7177    1.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2748    1.5229   -2.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1633    3.2396   -2.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5916    2.2353   -1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1008    1.1829   -1.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1031    1.5528    1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7068    1.1438    1.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3945   -1.2157    1.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5717   -4.0141    2.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4065   -6.0288    1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4288   -5.8563   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120   -3.5972   -0.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5993   -1.3888   -1.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0970    0.2528   -1.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9472   -1.4669    0.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6752    0.3483    1.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4126    0.8781    1.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7071    3.2721    1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8535    3.1757   -0.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3811    1.7212    0.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1446    2.8293   -0.9629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8154    0.0111   -0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    1.1451   -2.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 14  6  2  0
 25 16  1  0
 13  8  1  0
 24 20  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  7 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  1
 17 44  1  0
 20 45  1  1
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.595   2.083   0.769  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.852   1.868  -0.491  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.471   2.246  -1.778  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.655   1.344  -0.462  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.976   0.936   0.818  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.740  -0.520   0.719  0.00  0.00           C+0
HETATM    7  N   UNK     0      -2.559  -1.424   1.310  0.00  0.00           N+0
HETATM    8  C   UNK     0      -2.182  -2.682   1.033  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.697  -3.907   1.403  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.052  -5.031   0.935  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.937  -4.954   0.129  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.458  -3.721  -0.215  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.068  -2.561   0.229  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.782  -1.217   0.027  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.375  -0.719  -0.728  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.628  -0.503   0.070  0.00  0.00           C+0
HETATM   17  N   UNK     0       1.445   0.431   1.145  0.00  0.00           N+0
HETATM   18  C   UNK     0       2.392   1.485   1.286  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.043   2.542   1.836  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.781   1.348   0.795  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.432   2.656   0.416  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.679   2.106  -0.300  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.130   0.878  -1.024  0.00  0.00           C+0
HETATM   24  N   UNK     0       3.826   0.642  -0.464  0.00  0.00           N+0
HETATM   25  C   UNK     0       2.696  -0.079  -0.890  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.542  -0.399  -2.126  0.00  0.00           O+0
HETATM   27  H   UNK     0      -5.636   2.432   0.602  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.703   1.061   1.237  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.034   2.718   1.464  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.275   1.523  -2.594  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.163   3.240  -2.148  0.00  0.00           H+0
HETATM   32  H   UNK     0      -5.592   2.235  -1.647  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.101   1.183  -1.370  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.103   1.553   1.010  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.707   1.144   1.621  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.394  -1.216   1.915  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.572  -4.014   2.035  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.406  -6.029   1.190  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.429  -5.856  -0.239  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.412  -3.597  -0.843  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.599  -1.389  -1.616  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.097   0.253  -1.240  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.947  -1.467   0.581  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.675   0.348   1.810  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.413   0.878   1.567  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.707   3.272   1.288  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.853   3.176  -0.353  0.00  0.00           H+0
HETATM   48  H   UNK     0       6.381   1.721   0.470  0.00  0.00           H+0
HETATM   49  H   UNK     0       6.145   2.829  -0.963  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.815   0.011  -0.916  0.00  0.00           H+0
HETATM   51  H   UNK     0       5.123   1.145  -2.093  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   30   31   32                                             
CONECT    4    2    5   33                                                  
CONECT    5    4    6   34   35                                             
CONECT    6    5    7   14                                                  
CONECT    7    6    8   36                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10   37                                                  
CONECT   10    9   11   38                                                  
CONECT   11   10   12   39                                                  
CONECT   12   11   13   40                                                  
CONECT   13   12   14    8                                                  
CONECT   14   13   15    6                                                  
CONECT   15   14   16   41   42                                             
CONECT   16   15   17   25   43                                             
CONECT   17   16   18   44                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24   45                                             
CONECT   21   20   22   46   47                                             
CONECT   22   21   23   48   49                                             
CONECT   23   22   24   50   51                                             
CONECT   24   23   25   20                                                  
CONECT   25   24   26   16                                                  
CONECT   26   25                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    5                                                            
CONECT   36    7                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   16                                                            
CONECT   44   17                                                            
CONECT   45   20                                                            
CONECT   46   21                                                            
CONECT   47   21                                                            
CONECT   48   22                                                            
CONECT   49   22                                                            
CONECT   50   23                                                            
CONECT   51   23                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  108    0
END

RDKit          3D

51 54  0  0  0  0  0  0  0  0999 V2000
   -4.5948    2.0830    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8518    1.8680   -0.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4708    2.2460   -1.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6546    1.3438   -0.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9756    0.9360    0.8182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7398   -0.5203    0.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5590   -1.4236    1.3096 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1819   -2.6822    1.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6972   -3.9067    1.4035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0519   -5.0314    0.9350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9368   -4.9540    0.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4577   -3.7212   -0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681   -2.5612    0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7815   -1.2170    0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3747   -0.7191   -0.7281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6277   -0.5029    0.0703 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4453    0.4311    1.1446 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3924    1.4846    1.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427    2.5420    1.8357 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806    1.3477    0.7951 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4318    2.6556    0.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6787    2.1064   -0.2996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299    0.8778   -1.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8264    0.6417   -0.4638 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6959   -0.0788   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424   -0.3991   -2.1259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6362    2.4319    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7028    1.0612    1.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    2.7177    1.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2748    1.5229   -2.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1633    3.2396   -2.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5916    2.2353   -1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1008    1.1829   -1.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1031    1.5528    1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7068    1.1438    1.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3945   -1.2157    1.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5717   -4.0141    2.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4065   -6.0288    1.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4288   -5.8563   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120   -3.5972   -0.8432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5993   -1.3888   -1.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0970    0.2528   -1.2401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9472   -1.4669    0.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6752    0.3483    1.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4126    0.8781    1.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7071    3.2721    1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8535    3.1757   -0.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3811    1.7212    0.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1446    2.8293   -0.9629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8154    0.0111   -0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228    1.1451   -2.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 14  6  2  0
 25 16  1  0
 13  8  1  0
 24 20  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  7 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  1
 17 44  1  0
 20 45  1  1
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Triprostatin b	ChEBI

Chemical Formula

C₂₁H₂₅N₃O₂

Average Mass

351.4500 Da

Monoisotopic Mass

351.19468 Da

IUPAC Name

(3S,8aS)-3-{[2-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-octahydropyrrolo[1,2-a]pyrazine-1,4-dione

Traditional Name

(3S,8aS)-3-{[2-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(C[C@@H]2NC(=O)[C@@H]3CCCN3C2=O)C2=CC=CC=C2N1

InChI Identifier

InChI=1S/C21H25N3O2/c1-13(2)9-10-17-15(14-6-3-4-7-16(14)22-17)12-18-21(26)24-11-5-8-19(24)20(25)23-18/h3-4,6-7,9,18-19,22H,5,8,10-12H2,1-2H3,(H,23,25)/t18-,19-/m0/s1

InChI Key

GLWYBXPXOSKQAW-OALUTQOASA-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
Aspergillus	NPAtlas	8698635
Aspergillus fischeri	Fungi	KNApSAcK
Aspergillus fumigatus	Fungi	KNApSAcK
Cordyceps tenuipes	LOTUS Database	35616633
Isaria tenuipes BCC12625	-	KNApSAcK

Species Where Detected

Species Name	Source	Reference
Aspergillus fumigatus BM 939	KNApSAcK Database	22123792

Chemical Taxonomy

Classification

Not classified

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	2.87	ALOGPS
logP	2.45	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	11.51	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.2 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	102.26 m³·mol⁻¹	ChemAxon
Polarizability	40.04 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

NPAtlas ID

NPA010659

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00016084

Chemspider ID

8038977

KEGG Compound ID

C20512

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9863281

PDB ID

Not Available

ChEBI ID

72760

Good Scents ID

Not Available

References

General References

Wang H, Usui T, Osada H, Ganesan A: Synthesis and evaluation of tryprostatin B and demethoxyfumitremorgin C analogues. J Med Chem. 2000 Apr 20;43(8):1577-85. doi: 10.1021/jm9905662. [PubMed:10780915 ]
Caballero E, Avendano C, Menendez JC: Brief total synthesis of the cell cycle inhibitor tryprostatin B and related preparation of its alanine analogue. J Org Chem. 2003 Sep 5;68(18):6944-51. doi: 10.1021/jo034703l. [PubMed:12946134 ]
Cardoso AS, Marques MM, Srinivasan N, Prabhakar S, Lobo AM, Rzepa HS: Studies in sigmatropic rearrangements of N-prenylindole derivatives--a formal enantiomerically pure synthesis of tryprostatin B. Org Biomol Chem. 2006 Nov 7;4(21):3966-72. doi: 10.1039/b606457d. Epub 2006 Sep 28. [PubMed:17047877 ]

Showing NP-Card for Tryprostatin B (NP0023194)

MOL for NP0023194 (Tryprostatin B)

3D MOL for NP0023194 (Tryprostatin B)

3D SDF for NP0023194 (Tryprostatin B)

3D-SDF for NP0023194 (Tryprostatin B)

PDB for NP0023194 (Tryprostatin B)

3D PDB for NP0023194 (Tryprostatin B)

SMILES for NP0023194 (Tryprostatin B)

INCHI for NP0023194 (Tryprostatin B)

Structure for NP0023194 (Tryprostatin B)

3D Structure for NP0023194 (Tryprostatin B)