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SMILES: CC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)N1CCN(CC1)c1ncc(cn1)C(F)(F)F)C(=O)C2

InChI Key: InChIKey=LNRFZPWGNHLMFR-FZKQIMNGSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50412579   
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))		BDBM50412579
PNG
(CHEMBL479828)
Show SMILES CC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)N1CCN(CC1)c1ncc(cn1)C(F)(F)F)C(=O)C2 |r,THB:28:27:5.4:1|
Show InChI InChI=1S/C19H25F3N4O3S/c1-17(2)13-3-4-18(17,15(27)9-13)12-30(28,29)26-7-5-25(6-8-26)16-23-10-14(11-24-16)19(20,21)22/h10-11,13H,3-9,12H2,1-2H3/t13-,18-/m1/s1
UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem

Similars
Article
PubMed
n/an/a 316n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Antagonist activity at human recombinant CXCR3 receptor expressed in CHO-K1 cells assessed as human IP10-induced calcium flux by FLIPR assay

Bioorg Med Chem Lett 19: 114-8 (2008)


Article DOI: 10.1016/j.bmcl.2008.11.008
BindingDB Entry DOI: 10.7270/Q29Z94R0
More data for this
Ligand-Target Pair