NP-MRD: Showing NP-Card for 3-methyl-2-butenoylpyrrothine (NP0004360)

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Record Information

Version

2.0

Created at

2020-12-09 01:50:52 UTC

Updated at

2021-07-15 16:48:58 UTC

NP-MRD ID

NP0004360

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-methyl-2-butenoylpyrrothine

Provided By

NPAtlas

Description

Senecioyl-pyrrothine belongs to the class of organic compounds known as n-arylamides. These are organic compounds that contain a carboxamide group that is N-linked to a aryl group. They have the generic structure RC(=O)N(R')H, R = organyl group and R'= aryl group. 3-methyl-2-butenoylpyrrothine is found in Saccharothrix. 3-methyl-2-butenoylpyrrothine was first documented in 2002 (PMID: 12374383). Based on a literature review very few articles have been published on senecioyl-pyrrothine.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118063D          

 29 30  0  0  0  0            999 V2000
    3.6049    1.0169    0.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -0.1359    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9772   -0.7375   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860   -0.6681   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2431   -0.1493   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    0.8095    0.6659 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1195   -0.7653   -0.6696 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -0.3658   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3436   -1.0020   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6412   -2.3268   -2.0960 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -2.1537   -2.0777 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419   -0.8311   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -0.3649   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    0.6378    0.2745 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000    1.5954    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461    0.6233    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0885    1.4592    1.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    1.8973    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6512    1.3510    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776    0.7016    1.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8613   -1.8207   -0.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7463   -0.5803    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495   -0.2262   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363   -1.5162   -1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2681   -1.5951   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7321   -0.3999   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0359    2.4903    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8695    1.1571    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    1.8997    1.9316 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  2  0  0  0  0
  5  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  1  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
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16  8  1  0  0  0  0
 13  9  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
 12 26  1  0  0  0  0
 15 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
M  END

     RDKit          3D

 29 30  0  0  0  0  0  0  0  0999 V2000
    3.6049    1.0169    0.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -0.1359    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9772   -0.7375   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860   -0.6681   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2431   -0.1493   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    0.8095    0.6659 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1195   -0.7653   -0.6696 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -0.3658   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3436   -1.0020   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6412   -2.3268   -2.0960 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -2.1537   -2.0777 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419   -0.8311   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -0.3649   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    0.6378    0.2745 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000    1.5954    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461    0.6233    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0885    1.4592    1.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    1.8973    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6512    1.3510    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776    0.7016    1.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8613   -1.8207   -0.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7463   -0.5803    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495   -0.2262   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363   -1.5162   -1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2681   -1.5951   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7321   -0.3999   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0359    2.4903    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8695    1.1571    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    1.8997    1.9316 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 16  8  1  0
 13  9  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  7 25  1  0
 12 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
M  END


  Mrv1652306242118063D          

 29 30  0  0  0  0            999 V2000
    3.6049    1.0169    0.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -0.1359    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9772   -0.7375   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860   -0.6681   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2431   -0.1493   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    0.8095    0.6659 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1195   -0.7653   -0.6696 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -0.3658   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3436   -1.0020   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6412   -2.3268   -2.0960 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -2.1537   -2.0777 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419   -0.8311   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -0.3649   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    0.6378    0.2745 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000    1.5954    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461    0.6233    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0885    1.4592    1.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    1.8973    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6512    1.3510    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776    0.7016    1.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8613   -1.8207   -0.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7463   -0.5803    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495   -0.2262   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363   -1.5162   -1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2681   -1.5951   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7321   -0.3999   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0359    2.4903    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8695    1.1571    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    1.8997    1.9316 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  2  0  0  0  0
  5  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  1  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
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16  8  1  0  0  0  0
 13  9  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  7 25  1  0  0  0  0
 12 26  1  0  0  0  0
 15 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004360

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N(C(=O)C([H])=C(C([H])([H])[H])C([H])([H])[H])C1=C2SSC([H])=C2N(C1=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H12N2O2S2/c1-6(2)4-8(14)12-9-10-7(5-16-17-10)13(3)11(9)15/h4-5H,1-3H3,(H,12,14)

> <INCHI_KEY>
JFEBCAJATWCFMT-UHFFFAOYSA-N

> <FORMULA>
C11H12N2O2S2

> <MOLECULAR_WEIGHT>
268.35

> <EXACT_MASS>
268.034019982

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
27.653678633084006

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methyl-N-{4-methyl-5-oxo-4H,5H-[1,2]dithiolo[4,3-b]pyrrol-6-yl}but-2-enamide

> <ALOGPS_LOGP>
1.61

> <JCHEM_LOGP>
0.8588026580000003

> <ALOGPS_LOGS>
-2.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.548284971730151

> <JCHEM_PKA_STRONGEST_BASIC>
-4.103982198597427

> <JCHEM_POLAR_SURFACE_AREA>
49.410000000000004

> <JCHEM_REFRACTIVITY>
74.9497

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.18e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methyl-N-{4-methyl-5-oxo-[1,2]dithiolo[4,3-b]pyrrol-6-yl}but-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 29 30  0  0  0  0  0  0  0  0999 V2000
    3.6049    1.0169    0.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -0.1359    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9772   -0.7375   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860   -0.6681   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2431   -0.1493   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    0.8095    0.6659 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1195   -0.7653   -0.6696 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -0.3658   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3436   -1.0020   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6412   -2.3268   -2.0960 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -2.1537   -2.0777 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419   -0.8311   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -0.3649   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    0.6378    0.2745 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000    1.5954    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461    0.6233    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0885    1.4592    1.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    1.8973    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6512    1.3510    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776    0.7016    1.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8613   -1.8207   -0.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7463   -0.5803    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495   -0.2262   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363   -1.5162   -1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2681   -1.5951   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7321   -0.3999   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0359    2.4903    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8695    1.1571    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    1.8997    1.9316 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 16  8  1  0
 13  9  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  7 25  1  0
 12 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  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       3.605   1.017   0.979  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.651  -0.136   0.049  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.977  -0.738  -0.359  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.586  -0.668  -0.445  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.243  -0.149  -0.105  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.163   0.810   0.666  0.00  0.00           O+0
HETATM    7  N   UNK     0       0.120  -0.765  -0.670  0.00  0.00           N+0
HETATM    8  C   UNK     0      -1.206  -0.366  -0.425  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.344  -1.002  -1.007  0.00  0.00           C+0
HETATM   10  S   UNK     0      -2.641  -2.327  -2.096  0.00  0.00           S+0
HETATM   11  S   UNK     0      -4.691  -2.154  -2.078  0.00  0.00           S+0
HETATM   12  C   UNK     0      -4.742  -0.831  -1.011  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.530  -0.365  -0.562  0.00  0.00           C+0
HETATM   14  N   UNK     0      -3.092   0.638   0.275  0.00  0.00           N+0
HETATM   15  C   UNK     0      -3.900   1.595   1.001  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.746   0.623   0.343  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.089   1.459   1.058  0.00  0.00           O+0
HETATM   18  H   UNK     0       3.162   1.897   0.494  0.00  0.00           H+0
HETATM   19  H   UNK     0       4.651   1.351   1.241  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.078   0.702   1.908  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.861  -1.821  -0.503  0.00  0.00           H+0
HETATM   22  H   UNK     0       5.746  -0.580   0.401  0.00  0.00           H+0
HETATM   23  H   UNK     0       5.250  -0.226  -1.319  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.636  -1.516  -1.127  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.268  -1.595  -1.332  0.00  0.00           H+0
HETATM   26  H   UNK     0      -5.732  -0.400  -0.721  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.036   2.490   0.348  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.870   1.157   1.326  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.378   1.900   1.932  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   21   22   23                                             
CONECT    4    2    5   24                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   25                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14    9                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   27   28   29                                             
CONECT   16   14   17    8                                                  
CONECT   17   16                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    7                                                            
CONECT   26   12                                                            
CONECT   27   15                                                            
CONECT   28   15                                                            
CONECT   29   15                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

RDKit          3D

29 30  0  0  0  0  0  0  0  0999 V2000
    3.6049    1.0169    0.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -0.1359    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9772   -0.7375   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860   -0.6681   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2431   -0.1493   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    0.8095    0.6659 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1195   -0.7653   -0.6696 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -0.3658   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3436   -1.0020   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6412   -2.3268   -2.0960 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6915   -2.1537   -2.0777 S   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7419   -0.8311   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5298   -0.3649   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    0.6378    0.2745 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000    1.5954    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461    0.6233    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0885    1.4592    1.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1621    1.8973    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6512    1.3510    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0776    0.7016    1.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8613   -1.8207   -0.5032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7463   -0.5803    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2495   -0.2262   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6363   -1.5162   -1.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2681   -1.5951   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7321   -0.3999   -0.7213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0359    2.4903    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8695    1.1571    1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    1.8997    1.9316 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 16  8  1  0
 13  9  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  7 25  1  0
 12 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-Methyl-2-butenoylpyrrothine	MeSH
3-Methyl-N-{4-methyl-5-oxo-4H,5H-[1,2]dithiolo[4,3-b]pyrrol-6-yl}but-2-enimidate	Generator

Chemical Formula

C₁₁H₁₂N₂O₂S₂

Average Mass

268.3500 Da

Monoisotopic Mass

268.03402 Da

IUPAC Name

3-methyl-N-{4-methyl-5-oxo-4H,5H-[1,2]dithiolo[4,3-b]pyrrol-6-yl}but-2-enamide

Traditional Name

3-methyl-N-{4-methyl-5-oxo-[1,2]dithiolo[4,3-b]pyrrol-6-yl}but-2-enamide

CAS Registry Number

Not Available

SMILES

CN1C(=O)C(NC(=O)C=C(C)C)=C2SSC=C12

InChI Identifier

InChI=1S/C11H12N2O2S2/c1-6(2)4-8(14)12-9-10-7(5-16-17-10)13(3)11(9)15/h4-5H,1-3H3,(H,12,14)

InChI Key

JFEBCAJATWCFMT-UHFFFAOYSA-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
Saccharothrix	NPAtlas	12374383

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-arylamides. These are organic compounds that contain a carboxamide group that is N-linked to a aryl group. They have the generic structure RC(=O)N(R')H, R = organyl group and R'= aryl group.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

N-arylamides

Direct Parent

N-arylamides

Alternative Parents

Substituents

N-arylamide
N-methylpyrrole
Substituted pyrrole
Pyrrole
Heteroaromatic compound
1,2-dithiole
Dithiole
Carboxamide group
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Carbonyl group
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
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	1.61	ALOGPS
logP	0.86	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	12.55	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.41 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	74.95 m³·mol⁻¹	ChemAxon
Polarizability	27.65 Å³	ChemAxon
Number of Rings	2	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

NPA016903

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

435689

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

497680

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lamari L, Zitouni A, Dob T, Sabaou N, Lebrihi A, Germain P, Seguin E, Tillequin F: New dithiolopyrrolone antibiotics from Saccharothrix sp. SA 233. II. Physicochemical properties and structure elucidation. J Antibiot (Tokyo). 2002 Aug;55(8):702-6. doi: 10.7164/antibiotics.55.702. [PubMed:12374383 ]

Showing NP-Card for 3-methyl-2-butenoylpyrrothine (NP0004360)

MOL for NP0004360 (3-methyl-2-butenoylpyrrothine)

3D MOL for NP0004360 (3-methyl-2-butenoylpyrrothine)

3D SDF for NP0004360 (3-methyl-2-butenoylpyrrothine)

3D-SDF for NP0004360 (3-methyl-2-butenoylpyrrothine)

PDB for NP0004360 (3-methyl-2-butenoylpyrrothine)

3D PDB for NP0004360 (3-methyl-2-butenoylpyrrothine)

SMILES for NP0004360 (3-methyl-2-butenoylpyrrothine)

INCHI for NP0004360 (3-methyl-2-butenoylpyrrothine)

Structure for NP0004360 (3-methyl-2-butenoylpyrrothine)

3D Structure for NP0004360 (3-methyl-2-butenoylpyrrothine)