ilacirnon   Click here for help

GtoPdb Ligand ID: 11185

Synonyms: CCX-140B | CCX140 | CCX140-B | CCX140B | Example 5 [WO2009009740A1]
Compound class: Synthetic organic
Comment: Ilacirnon (CCX140B) is a clinical stage, orally administered antagonist of the chemokine receptor CCR2 [3]. It was developed by Chemocentryx. The chemical structure of CCX140B matches that submitted to the WHO for the INN ilacirnon, and is one of those claimed in Chemocentryx's patent WO2009009740A1 [2]
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 7
Hydrogen bond donors 2
Rotatable bonds 6
Topological polar surface area 126.08
Molecular weight 495.04
XLogP 3.98
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES Cc1cnc(c(c1)NS(=O)(=O)c1ccc(c(c1)C(F)(F)F)Cl)C(=O)c1ncnc2c1cc[nH]2
Isomeric SMILES Cc1cnc(c(c1)NS(=O)(=O)c1ccc(c(c1)C(F)(F)F)Cl)C(=O)c1ncnc2c1cc[nH]2
InChI InChI=1S/C20H13ClF3N5O3S/c1-10-6-15(29-33(31,32)11-2-3-14(21)13(7-11)20(22,23)24)17(26-8-10)18(30)16-12-4-5-25-19(12)28-9-27-16/h2-9,29H,1H3,(H,25,27,28)
InChI Key LUUMLYXKTPBTQR-UHFFFAOYSA-N
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Summary of Clinical Use Click here for help
CCX140 was advanced to clinical evaluation, reaching Phase 2 for diabetic nephropathy and the rare kidney disorder focal segmental slomerulosclerosis (FSGS).
Clinical Trials
Clinical Trial ID Title Type Source Comment References
NCT01440257 A Study to Evaluate the Effect of CCX140-B on Urinary Albumin Excretion in Subjects With Type 2 Diabetes and Albuminuria Phase 2 Interventional ChemoCentryx
NCT03703908 A Study of CCX140-B in Subjects With Primary FSGS and Nephrotic Syndrome Phase 2 Interventional ChemoCentryx
NCT01447147 A Study to Evaluate the Safety and Efficacy of CCX140-B in Subjects With Diabetic Nephropathy Phase 2 Interventional ChemoCentryx 1
NCT03536754 A Study of CCX140-B in Subjects With FSGS Phase 2 Interventional ChemoCentryx This trial is known as the LUMINA-1 study. In mid-2020, Chemocentryx announced (on their company website) that this study had found no evidence of meaningful clinical efficacy in FSGS patients compared to placebo after 12 weeks of CCX140 treatment, and that the compound would not continue in FSGS.