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SMILES: Clc1ccc(cc1)S(=O)(=O)N(Cc1ccc(cc1)C(=O)NCC1CC1)Cc1cccc(Cl)c1

InChI Key: InChIKey=PAFIBRJMINLFRJ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50320143   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kcal/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
C-X-C chemokine receptor type 3


(Homo sapiens (Human))		BDBM50320143
PNG
(4-((4-chloro-N-(3-chlorobenzyl)phenylsulfonamido)m...)
Show SMILES Clc1ccc(cc1)S(=O)(=O)N(Cc1ccc(cc1)C(=O)NCC1CC1)Cc1cccc(Cl)c1
Show InChI InChI=1S/C25H24Cl2N2O3S/c26-22-10-12-24(13-11-22)33(31,32)29(17-20-2-1-3-23(27)14-20)16-19-6-8-21(9-7-19)25(30)28-15-18-4-5-18/h1-3,6-14,18H,4-5,15-17H2,(H,28,30)
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Article
PubMed
n/an/a 940n/an/an/an/an/an/a



Merck Serono SA

Curated by ChEMBL


Assay Description
Antagonist activity at human CXCR3 expressed in mouse L1.2 cells assessed as inhibition of IP10-induced chemotaxis after 4 hrs

Bioorg Med Chem Lett 20: 3614-7 (2010)


Article DOI: 10.1016/j.bmcl.2010.04.113
BindingDB Entry DOI: 10.7270/Q2668DDX
More data for this
Ligand-Target Pair