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CCR

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CCR

Chemical Structure Cat. No. Product Name CAS No.
Nifeviroc Chemical Structure
 BCP39005 Nifeviroc 934740-33-7
Nifeviroc is a CCR5 antagonist potentially for treatment of inflammatory responses to HIV type-1 infection
R243 Chemical Structure
 BCP37891 R243 688352-84-3
R243 is an inhibitor of CCR8 signaling and chemotaxis.
TAK-220 Chemical Structure
 BCP37344 TAK-220 333994-00-6
TAK-220 is an orally bioavailable small-molecule CCR5 antagonist
TAK-220 Hydrochloride Chemical Structure
 BCP37346 TAK-220 Hydrochloride 674782-27-5
TAK-220 is a selective and orally bioavailable CCR5 antagonist.
AZ084 Chemical Structure
 BCP34891 AZ084 929300-19-6
AZ084 is a potent, selective, allosteric, orally available CCR8 antagonist with Ki of 0.9 nM.
BX471 hydrochloride Chemical Structure
 BCP32594 BX471 hydrochloride 288262-96-4
BX471 hydrochloride is a potent, selective non-peptide CCR1 antagonist with Ki of 1 nM for human CCR1, and exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4.
J-113863, trans- Chemical Structure
 BCP27912 J-113863, trans- 353791-85-2
J 113863 is a potent CCR1 antagonist
CCX140-B Chemical Structure
 BCP25695 CCX140-B 1100318-47-5
CCX140-B is a potent CCR2 antagonist.
CP 481715 Chemical Structure
 BCP18399 CP 481715 212790-31-3
CP 481715 a potent and selective CCR1 antagonist with potential therapeutic implications for inflammatory diseases.
BX 513 hydrochloride Chemical Structure
 BCP27909 BX 513 hydrochloride 1216540-18-9
BX-513 hydrochloride inhibits MIP-1α-induced intracellular calcium mobilization (IC50 = 2.5 μM).
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