NP-MRD: Showing NP-Card for 3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol (NP0322970)

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Record Information

Version

2.0

Created at

2022-09-12 02:05:26 UTC

Updated at

2022-09-12 02:05:26 UTC

NP-MRD ID

NP0322970

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol

Description

Rhopaladin A belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. Indolecarboxylic acids and derivatives are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole. Based on a literature review very few articles have been published on Rhopaladin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122204052D          

 29 33  0  0  0  0            999 V2000
    1.4358   -2.7631    0.0000 O   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
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   -3.0752    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -2.9890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6313   -3.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -2.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0044   -1.8464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6719   -2.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6719   -3.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4565   -3.4113    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9414   -2.7439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7619   -2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0975   -1.9040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9179   -1.8177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6125   -1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7920   -1.3227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4565   -2.0764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -1.7695    0.0000 N   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
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 Br  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  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  8  7  1  4  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
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
  9 18  1  0  0  0  0
  7 19  1  0  0  0  0
  3 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 20 29  1  0  0  0  0
 23 29  1  0  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -3.1746   -1.3840    1.6718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4507   -0.7637    0.8367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.2101    0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3517   -1.8266    1.6873 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8770   -2.0927    1.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8800   -2.7181    1.9828 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881   -1.6363   -0.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1260   -1.6972   -0.9258 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3270   -1.2162   -0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4170   -1.3738   -1.7921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4573   -0.7572   -1.3805 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2572   -0.1343   -0.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0985    0.6405    0.6599 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6341    1.1519    1.8453 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4588    1.9363    2.6708 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3375    0.8844    2.2198 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5040    0.1180    1.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9439   -0.4070    0.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2410   -1.1032   -0.3276 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0298    0.3244    0.0725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4026    1.3387   -0.6309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3523    2.1236   -1.1807 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5803    1.6762   -0.8744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8682    2.0833   -1.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9655    1.4034   -0.6905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7591    0.2927    0.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2370   -0.6893    0.7640 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -5.4936   -0.1198    0.3732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3833    0.5537   -0.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.6720    1.7351 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9063   -2.2584   -1.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3139   -1.9270   -2.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1261    0.8430    0.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4563    2.9355    2.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9731    1.2912    3.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4921   -0.0645    1.7238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4446   -0.6840   -1.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3399    1.4688   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2139    2.9880   -1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0313    2.9641   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9964    1.7143   -0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3674   -0.9966    0.9836 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  7  2  0
  7 19  1  0
 19  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  0
  2 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  2  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
 14 16  2  0
 16 17  1  0
 17 18  2  0
  4  5  1  0
 29 20  1  0
 18  9  1  0
 29 23  1  0
 18 12  1  0
  6 30  1  0
 19 37  1  0
 21 38  1  0
 22 39  1  0
 24 40  1  0
 25 41  1  0
 28 42  1  0
  8 31  1  0
 10 32  1  0
 13 33  1  0
 15 34  1  0
 16 35  1  0
 17 36  1  0
M  END


  Mrv1652309122204052D          

 29 33  0  0  0  0            999 V2000
    1.4358   -2.7631    0.0000 O   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
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   -3.0752    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -2.9890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6313   -3.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -2.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0044   -1.8464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6719   -2.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6719   -3.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4565   -3.4113    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9414   -2.7439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7619   -2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0975   -1.9040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9179   -1.8177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6125   -1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7920   -1.3227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4565   -2.0764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -1.7695    0.0000 N   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
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 Br  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  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  8  7  1  4  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
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
  9 18  1  0  0  0  0
  7 19  1  0  0  0  0
  3 19  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 20 29  1  0  0  0  0
 23 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322970

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=C(NC(=N1)C(=O)C1=CNC2=CC=C(Br)C=C12)C=C1C=NC2=CC(O)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C21H13BrN4O3/c22-11-1-4-16-14(6-11)15(9-24-16)19(28)20-25-18(21(29)26-20)5-10-8-23-17-7-12(27)2-3-13(10)17/h1-9,24,27,29H,(H,25,26)

> <INCHI_KEY>
ZNEDGUYAWZIBJL-UHFFFAOYSA-N

> <FORMULA>
C21H13BrN4O3

> <MOLECULAR_WEIGHT>
449.264

> <EXACT_MASS>
448.017103

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
42.54751668337026

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[2-(5-bromo-1H-indole-3-carbonyl)-4-hydroxy-1H-imidazol-5-yl]methylidene}-3H-indol-6-ol

> <JCHEM_LOGP>
4.327341085333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.213442398875507

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.612592492044769

> <JCHEM_PKA_STRONGEST_BASIC>
3.504541176982228

> <JCHEM_POLAR_SURFACE_AREA>
114.35999999999999

> <JCHEM_REFRACTIVITY>
115.14380000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-{[2-(5-bromo-1H-indole-3-carbonyl)-5-hydroxy-3H-imidazol-4-yl]methylidene}indol-6-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  O   UNK     0       2.680  -5.158   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -0.483  -5.740   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -2.015  -5.579   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.045  -6.724   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.335  -4.073   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.742  -3.447   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.987  -4.352   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.987  -5.892   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -6.452  -6.368   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -7.357  -5.122   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -8.889  -4.961   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.515  -3.554   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -11.047  -3.393   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -8.610  -2.308   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.078  -2.469   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.452  -3.876   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      -1.001  -3.303   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   27 Br   UNK     0       7.591  -2.843   0.000  0.00  0.00          Br+0
HETATM   28  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12    9                                                  
CONECT   19    7    3                                                       
CONECT   20    2   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   20   23                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₃BrN₄O₃

Average Mass

449.2640 Da

Monoisotopic Mass

448.01710 Da

IUPAC Name

3-{[2-(5-bromo-1H-indole-3-carbonyl)-4-hydroxy-1H-imidazol-5-yl]methylidene}-3H-indol-6-ol

Traditional Name

3-{[2-(5-bromo-1H-indole-3-carbonyl)-5-hydroxy-3H-imidazol-4-yl]methylidene}indol-6-ol

CAS Registry Number

Not Available

SMILES

OC1=C(NC(=N1)C(=O)C1=CNC2=CC=C(Br)C=C12)C=C1C=NC2=CC(O)=CC=C12

InChI Identifier

InChI=1S/C21H13BrN4O3/c22-11-1-4-16-14(6-11)15(9-24-16)19(28)20-25-18(21(29)26-20)5-10-8-23-17-7-12(27)2-3-13(10)17/h1-9,24,27,29H,(H,25,26)

InChI Key

ZNEDGUYAWZIBJL-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 indolecarboxylic acids and derivatives. Indolecarboxylic acids and derivatives are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolecarboxylic acids and derivatives

Direct Parent

Indolecarboxylic acids and derivatives

Alternative Parents

Substituents

Indolecarboxylic acid derivative
Indole
Aryl ketone
Trisubstituted imidazole
2,4,5-trisubstituted-imidazole
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Substituted pyrrole
Aryl halide
Aryl bromide
Heteroaromatic compound
Vinylogous amide
Pyrrole
Imidazole
Azole
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organobromide
Organohalogen compound
Imine
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	4.33	ChemAxon
pKa (Strongest Acidic)	8.61	ChemAxon
pKa (Strongest Basic)	3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	114.36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	115.14 m³·mol⁻¹	ChemAxon
Polarizability	42.55 Å³	ChemAxon
Number of Rings	5	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00026866

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

136691194

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol (NP0322970)

MOL for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

3D MOL for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

3D SDF for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

3D-SDF for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

PDB for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

3D PDB for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

SMILES for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

INCHI for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

Structure for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)

3D Structure for NP0322970 (3-{[2-(5-bromo-1h-indole-3-carbonyl)-5-hydroxy-3h-imidazol-4-yl]methylidene}indol-6-ol)