General Information of the Compound
Compound ID
CP0875996
Compound Name
3-(1H-imidazol-4-yl)propyl N-benzyl-N'-(4-chlorobenzyl)carbamimidothioate dihydrobromide
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Structure
Formula
C21H24BrClN4S
Molecular Weight
479.875
Canonical SMILES
Br.Clc1ccc(C/N=C(/NCc2ccccc2)SCCCc2c[nH]cn2)cc1
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InChI
InChI=1S/C21H23ClN4S.BrH/c22-19-10-8-18(9-11-19)14-25-21(24-13-17-5-2-1-3-6-17)27-12-4-7-20-15-23-16-26-20;/h1-3,5-6,8-11,15-16H,4,7,12-14H2,(H,23,26)(H,24,25);1H
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InChIKey
SBJSQILUNRNHEF-UHFFFAOYSA-N
Physicochemical Property
logP
5.6528
Rotatable Bonds
8
Heavy Atom Count
28
Polar Areas
53.07
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Complexity
28

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 57401301
ChEMBL ID
CHEMBL1923028
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01194, Histamine H3 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 16.98 nM
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   LI
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   TS
Protein ID: PT01711, Histamine H4 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 229.09 nM
   TI
   LI
   LO
   TS