|M9944||7,4'-Dihydroxyflavone||7,4'-Dihydroxyflavone, a flavonoid isolated from Glycyrrhiza uralensis, is an eotaxin/CCL11 inhibitor.|
|M9884||INCB3284||INCB3284 is a potent, selective, and orally bioavailable hCCR2 antagonist, exhibited an IC50 of 3.7 nM in antagonism of monocyte chemoattractant protein-1 binding to hCCR2.|
|M9444||Cenicriviroc Mesylate||Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, and it also inhibits both HIV-1 and HIV-2.|
|M9135||TAK-779||TAK-779 is a potent and selective nonpeptide antagonist of CCR5, with a Ki of 1.1 nM for CCR5.|
|M9131||ZK-756326 dihydrochloride||ZK-756326 dihydrochloride is a potent, selective and non-peptide CCR8 chemokine receptor agonist.|
|M9006||NSC5844||NSC5844 (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic properties.|
|M8986||CCX140||CCX140 is a potent CCR2 antagonist.|
|M8254||SB 297006||SB 297006 is an antagonist of CCR3 with IC50 of 39 nM.|
|M7224||RS 504393||RS 504393 is a highly selective CCR2 chemokine receptor antagonist.|
|M6547||BX 471||BX 471 is a potent, selective CCR1 antagonist.|
|M6263||INCB3284 dimesylate||INCB 3284 dimesylate is a potent, selective and orally bioavailable hCCR2 antagonist with IC50 of 3.7 nM.|
|M6249||BMS-813160||BMS-813160 is the first dual CCR2/CCR5 antagonist to enter clinical development for cardiovascular.|
|M2032||Vicriviroc Malate||Vicriviroc (SCH 417690) is a pyrimidine CCR5 entry inhibitor of HIV-1 with IC50 of 0.91 nM.|
|M1971||Maraviroc||Maraviroc (UK-427857) is a selective CCR5 antagonist with potent anti-human immunodeficiency virus type 1 (HIV-1) activity and favorable pharmacological properties.|
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