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CCR

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CCR

Chemical Structure Cat. No. Product Name CAS No.
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).
UCB 35625 Chemical Structure
BCP27911 UCB 35625 301648-08-8
UCB35625 is a potent chemokine CKR-1 (CCR1) and CKR-3 (CCR3) receptor antagonist.
ZK-756326 Chemical Structure
BCP20725 ZK-756326 874911-96-3
ZK-756326 is a potent, selective and non-peptide CCR8 chemokine receptor agonist.
ZK756326 dihydrochloride Chemical Structure
BCP29859 ZK756326 dihydrochloride 1780259-94-0
ZK756326 dihydrochloride is a nonpeptide chemokine receptor agonist for the CC chemokine receptor CCR8.
SB-297006 Chemical Structure
BCP29726 SB-297006 58816-69-6
SB-297006 is a potent and selective CCR3 antagonist (IC50 = 39 nM).
GSK2239633A Chemical Structure
BCP29621 GSK2239633A 1240516-71-5
GSK2239633A is a CC-chemokine receptor 4 (CCR4) antagonist, which inhibits the binding of [125I]-TARC to human CCR4 with a pIC50 of 7.96 ± 0.11.
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