NP-MRD: Showing NP-Card for n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid (NP0272238)

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Record Information

Version

2.0

Created at

2022-09-08 18:47:42 UTC

Updated at

2022-09-08 18:47:42 UTC

NP-MRD ID

NP0272238

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid

Description

N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-4-(butan-2-yl)-5-oxo-2-(propan-2-yl)-2,5-dihydro-1H-imidazole-2-carboximidic acid belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-4-(butan-2-yl)-5-oxo-2-(propan-2-yl)-2,5-dihydro-1H-imidazole-2-carboximidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241505402D          

 28 30  0  0  0  0            999 V2000
   -3.0361   -5.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5582   -6.2161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369   -6.1385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2590   -6.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3935   -5.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7985   -4.6696    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4899   -4.4057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5847   -5.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225   -5.7837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7791   -3.4378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078   -2.6587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5895   -3.5924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0713   -2.4572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    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  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 19 28  1  0  0  0  0
 22 28  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -4.1638    1.6298    1.7771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7984    2.5777    0.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0584    2.0471   -0.6914 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5153    1.7373   -0.8481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1964    0.8331   -0.9325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622    0.3042   -0.1220 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6830   -0.8531   -0.6363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2184   -0.6319   -0.7600 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2742   -0.6016   -1.8904 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5136   -0.4715    0.4118 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9323   -0.2459    0.5699 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7634   -0.1576   -0.4183 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1996    0.0631   -0.4416 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9647    0.1381   -1.6274 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2229    0.3439   -1.2876 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3422    0.4100    0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4673    0.6120    0.8494 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3595    0.6442    2.2155 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8579    0.9157    3.3629 Br  0  0  0  0  0  0  0  0  0  0  0  0
    6.1181    0.4731    2.7671 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9962    0.2715    1.9527 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1040    0.2389    0.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0246   -2.0086    0.2587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4048   -3.3029   -0.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5281   -2.1893    0.2854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2344   -0.9919   -1.9615 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1723    0.0492   -2.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8619    0.2757   -3.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5463    1.7579    2.6969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2104    1.8313    2.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1462    0.5763    1.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7365    2.9091    0.8052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4061    3.5015    0.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7413    2.8091   -1.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8921    1.9848   -1.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0782    2.2486   -0.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6849    0.6472   -0.7217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0087   -0.5107    1.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3005   -0.1475    1.5769 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3374   -0.2658   -1.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5791    0.0433   -2.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0683    0.4509   -1.9268 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4410    0.7463    0.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0086    0.4946    3.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0545    0.1423    2.4034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7198   -1.7689    1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0666   -4.1842    0.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2521   -3.3980   -1.2388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4366   -3.5152    0.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8215   -3.2124    0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0403   -1.5043   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9642   -1.9970    1.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9491   -1.7493   -2.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7 26  1  0
 26 27  1  0
 27 28  2  0
  7 23  1  0
 23 24  1  0
 23 25  1  0
  7  8  1  6
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  2  0
 27  5  1  0
 22 13  1  0
 22 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  6
  4 35  1  0
  4 36  1  0
  4 37  1  0
 26 53  1  0
 23 46  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 14 41  1  0
 15 42  1  0
 17 43  1  0
 20 44  1  0
 21 45  1  0
M  END


  Mrv1533004241505402D          

 28 30  0  0  0  0            999 V2000
   -3.0361   -5.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5582   -6.2161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369   -6.1385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2590   -6.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3935   -5.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7985   -4.6696    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4899   -4.4057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5847   -5.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225   -5.7837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7791   -3.4378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078   -2.6587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5895   -3.5924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0713   -2.4572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    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  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 19 28  1  0  0  0  0
 22 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0272238

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C1=NC(NC1=O)(C(C)C)C(=O)NC=CC1=CNC2=CC(Br)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C21H25BrN4O2/c1-5-13(4)18-19(27)26-21(25-18,12(2)3)20(28)23-9-8-14-11-24-17-10-15(22)6-7-16(14)17/h6-13,24H,5H2,1-4H3,(H,23,28)(H,26,27)

> <INCHI_KEY>
BYSHQQIXWYAENH-UHFFFAOYSA-N

> <FORMULA>
C21H25BrN4O2

> <MOLECULAR_WEIGHT>
445.361

> <EXACT_MASS>
444.116089

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
44.71693606366662

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-4-(butan-2-yl)-5-oxo-2-(propan-2-yl)-2,5-dihydro-1H-imidazole-2-carboxamide

> <ALOGPS_LOGP>
4.19

> <JCHEM_LOGP>
5.100071496000001

> <ALOGPS_LOGS>
-5.39

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.648656708548415

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.52022697913392

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6257537262437447

> <JCHEM_POLAR_SURFACE_AREA>
86.35

> <JCHEM_REFRACTIVITY>
113.26410000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3H-imidazole-2-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.667 -10.348   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.775 -11.603   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.242 -11.458   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.350 -12.714   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.601 -10.058   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -3.357  -8.717   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -2.315  -7.583   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -0.915  -8.224   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -1.092  -9.754   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.042 -10.796   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.321  -6.417   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.815  -4.963   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.834  -6.706   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.000  -4.587   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0      -0.333  -5.798   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   25 Br   UNK     0       7.591   0.237   0.000  0.00  0.00          Br+0
HETATM   26  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11   14                                             
CONECT    8    7    9                                                       
CONECT    9    8    5   10                                                  
CONECT   10    9                                                            
CONECT   11    7   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    7   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   19   22                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
N-[2-(6-Bromo-1H-indol-3-yl)ethenyl]-4-(butan-2-yl)-5-oxo-2-(propan-2-yl)-2,5-dihydro-1H-imidazole-2-carboximidate	Generator

Chemical Formula

C₂₁H₂₅BrN₄O₂

Average Mass

445.3610 Da

Monoisotopic Mass

444.11609 Da

IUPAC Name

N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-4-(butan-2-yl)-5-oxo-2-(propan-2-yl)-2,5-dihydro-1H-imidazole-2-carboxamide

Traditional Name

N-[2-(6-bromo-1H-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3H-imidazole-2-carboxamide

CAS Registry Number

Not Available

SMILES

CCC(C)C1=NC(NC1=O)(C(C)C)C(=O)NC=CC1=CNC2=CC(Br)=CC=C12

InChI Identifier

InChI=1S/C21H25BrN4O2/c1-5-13(4)18-19(27)26-21(25-18,12(2)3)20(28)23-9-8-14-11-24-17-10-15(22)6-7-16(14)17/h6-13,24H,5H2,1-4H3,(H,23,28)(H,26,27)

InChI Key

BYSHQQIXWYAENH-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Aryl bromide
Aryl halide
Imidazolinone
Benzenoid
Substituted pyrrole
3-imidazoline
Heteroaromatic compound
Pyrrole
Carboxamide group
Ketimine
Secondary carboxylic acid amide
Lactam
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Imine
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Organooxygen compound
Organohalogen compound
Organobromide
Organonitrogen 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	4.19	ALOGPS
logP	5.1	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	10.52	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.35 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	113.26 m³·mol⁻¹	ChemAxon
Polarizability	44.72 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

85116006

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid (NP0272238)

MOL for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

3D MOL for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

3D SDF for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

3D-SDF for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

PDB for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

3D PDB for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

SMILES for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

INCHI for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

Structure for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)

3D Structure for NP0272238 (n-[2-(6-bromo-1h-indol-3-yl)ethenyl]-2-isopropyl-4-oxo-5-(sec-butyl)-3h-imidazole-2-carboximidic acid)