NP-MRD: Showing NP-Card for 5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole (NP0230908)

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Record Information

Version

2.0

Created at

2022-09-06 11:31:31 UTC

Updated at

2022-09-06 11:31:31 UTC

NP-MRD ID

NP0230908

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole

Description

5-Chloro-3-[4-(5-chloro-1,3-dimethyl-2,3-dihydro-1H-indol-3-yl)-1-methyl-1H-pyrrol-3-yl]-1H-indole 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. Based on a literature review very few articles have been published on 5-chloro-3-[4-(5-chloro-1,3-dimethyl-2,3-dihydro-1H-indol-3-yl)-1-methyl-1H-pyrrol-3-yl]-1H-indole.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062213312D          

 28 32  0  0  0  0            999 V2000
    2.4462    3.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7011    2.4415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2162    1.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7011    1.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866    0.6942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0367    0.3530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8436    0.1815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299   -0.6390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6443   -1.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242   -0.3615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8037   -0.4477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5842   -0.9907    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4980   -0.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1695    0.3147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0832    1.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6705    1.4708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7567    2.2912    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3379    0.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2517    0.1654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    1.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002    0.9491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9147    1.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6291    0.9491    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.9147    2.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002    2.5991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    2.1866    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
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 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
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 21  1  0  0  0  0
 15 21  1  0  0  0  0
  4 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
 22 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
   -4.3054   -0.7494   -0.6792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0808   -0.0751   -1.0357 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2154   -0.4916   -2.1241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8155   -0.1166   -1.6889 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0645    0.2133   -2.9336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2492   -1.1939   -0.8592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728   -2.4084   -0.6620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1297   -3.1716    0.1763 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4993   -4.5297    0.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9392   -2.4650    0.5060 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8968   -1.2382   -0.1179 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2571   -0.0154 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6766    0.3338   -1.0068 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5814    1.1878   -0.4802 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284    1.1639    0.8775 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1078    1.8651    1.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7849    1.7014    3.2115 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7676    0.8153    3.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3428    0.5940    5.2060 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.1118    0.1336    2.5055 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4137    0.2796    1.1587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1029    1.1096   -0.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3648    2.1719   -0.4300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042    3.1864    0.3505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047    4.5182    0.8683 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.2299    3.1514    0.7186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9925    2.0823    0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4420    1.0717   -0.4954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1201   -0.4613   -1.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6140   -0.4983    0.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2208   -1.8487   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3005   -1.5109   -2.4476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5262    0.1629   -2.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7291    0.3759   -3.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -0.6325   -3.2162 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4951    1.1690   -2.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8266   -2.7850   -1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0361   -4.4238    1.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1511   -4.9843   -0.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4660   -5.0671    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7196   -2.8493    1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6227    0.1873   -2.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2801    1.7714   -0.9867 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8884    2.5391    1.5597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3126    2.2483    3.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3278   -0.5464    2.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6683    2.2780   -0.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6469    3.9395    1.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0279    2.0535    0.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8 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  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 11  6  1  0
  6  7  2  0
  6  4  1  0
  4  5  1  6
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 28  1  0
 28 27  2  0
 27 26  1  0
 26 24  2  0
 24 25  1  0
 24 23  1  0
 23 22  2  0
  7  8  1  0
 22  4  1  0
 21 12  1  0
 22 28  1  0
 21 15  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 13 42  1  0
 14 43  1  0
 16 44  1  0
 17 45  1  0
 20 46  1  0
  7 37  1  0
  5 34  1  0
  5 35  1  0
  5 36  1  0
  3 32  1  0
  3 33  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 27 49  1  0
 26 48  1  0
 23 47  1  0
M  END


  Mrv1652309062213312D          

 28 32  0  0  0  0            999 V2000
    2.4462    3.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7011    2.4415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2162    1.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7011    1.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866    0.6942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0367    0.3530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8436    0.1815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9299   -0.6390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6443   -1.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242   -0.3615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8037   -0.4477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3912   -1.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5842   -0.9907    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4980   -0.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1695    0.3147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0832    1.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6705    1.4708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7567    2.2912    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3379    0.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2517    0.1654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    1.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002    0.9491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9147    1.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6291    0.9491    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.9147    2.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002    2.5991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    2.1866    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
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 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
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 21  1  0  0  0  0
 15 21  1  0  0  0  0
  4 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
 22 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230908

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C=C(C2=CNC3=CC=C(Cl)C=C23)C(=C1)C1(C)CN(C)C2=CC=C(Cl)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C23H21Cl2N3/c1-23(13-28(3)22-7-5-15(25)9-19(22)23)20-12-27(2)11-18(20)17-10-26-21-6-4-14(24)8-16(17)21/h4-12,26H,13H2,1-3H3

> <INCHI_KEY>
CMOISPAWONHXEH-UHFFFAOYSA-N

> <FORMULA>
C23H21Cl2N3

> <MOLECULAR_WEIGHT>
410.34

> <EXACT_MASS>
409.1112531

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
44.23686994818773

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-chloro-3-[4-(5-chloro-1,3-dimethyl-2,3-dihydro-1H-indol-3-yl)-1-methyl-1H-pyrrol-3-yl]-1H-indole

> <JCHEM_LOGP>
6.255592716

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.609545881207907

> <JCHEM_PKA_STRONGEST_BASIC>
3.356327844383608

> <JCHEM_POLAR_SURFACE_AREA>
23.96

> <JCHEM_REFRACTIVITY>
128.7431

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-chloro-3-[4-(5-chloro-1,3-dimethyl-2H-indol-3-yl)-1-methylpyrrol-3-yl]-1H-indole

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.566   6.022   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       5.042   4.558   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       4.137   3.312   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.042   2.066   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.708   1.296   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.668   0.659   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.175   0.339   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       7.336  -1.193   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       8.669  -1.963   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.929  -1.819   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.898  -0.675   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.367  -0.836   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.597  -2.169   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       1.091  -1.849   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       0.930  -0.318   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.316   0.587   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.155   2.119   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.252   2.745   0.000  0.00  0.00           C+0
HETATM   19 Cl   UNK     0       1.412   4.277   0.000  0.00  0.00          Cl+0
HETATM   20  C   UNK     0       2.497   1.840   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.336   0.309   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.507   2.542   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.840   1.772   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.174   2.542   0.000  0.00  0.00           C+0
HETATM   25 Cl   UNK     0      10.508   1.772   0.000  0.00  0.00          Cl+0
HETATM   26  C   UNK     0       9.174   4.082   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.840   4.852   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.507   4.082   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   22                                             
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   12   15                                                  
CONECT   22    4   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   22    2                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₁Cl₂N₃

Average Mass

410.3400 Da

Monoisotopic Mass

409.11125 Da

IUPAC Name

5-chloro-3-[4-(5-chloro-1,3-dimethyl-2,3-dihydro-1H-indol-3-yl)-1-methyl-1H-pyrrol-3-yl]-1H-indole

Traditional Name

5-chloro-3-[4-(5-chloro-1,3-dimethyl-2H-indol-3-yl)-1-methylpyrrol-3-yl]-1H-indole

CAS Registry Number

Not Available

SMILES

CN1C=C(C2=CNC3=CC=C(Cl)C=C23)C(=C1)C1(C)CN(C)C2=CC=C(Cl)C=C12

InChI Identifier

InChI=1S/C23H21Cl2N3/c1-23(13-28(3)22-7-5-15(25)9-19(22)23)20-12-27(2)11-18(20)17-10-26-21-6-4-14(24)8-16(17)21/h4-12,26H,13H2,1-3H3

InChI Key

CMOISPAWONHXEH-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
Tertiary aliphatic/aromatic amine
Dialkylarylamine
Aralkylamine
Aryl chloride
Aryl halide
N-methylpyrrole
Substituted pyrrole
Benzenoid
Pyrrole
Heteroaromatic compound
Tertiary amine
Azacycle
Organonitrogen compound
Organochloride
Organohalogen compound
Amine
Hydrocarbon derivative
Organic nitrogen 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	6.26	ChemAxon
pKa (Strongest Acidic)	15.61	ChemAxon
pKa (Strongest Basic)	3.36	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	23.96 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	128.74 m³·mol⁻¹	ChemAxon
Polarizability	44.24 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

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

101914680

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole (NP0230908)

MOL for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

3D MOL for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

3D SDF for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

3D-SDF for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

PDB for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

3D PDB for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

SMILES for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

INCHI for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

Structure for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)

3D Structure for NP0230908 (5-chloro-3-[4-(5-chloro-1,3-dimethyl-2h-indol-3-yl)-1-methylpyrrol-3-yl]-1h-indole)