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Chemical Structure Cat. No. Product Name CAS No.
JMS-17-2 Chemical Structure
BCP31312 JMS-17-2 1380392-05-1
JMS-17-2 is a potent and selective antagonist of CX3CR1.
Elubrixin hydrochloride Chemical Structure
BCP23554 Elubrixin hydrochloride 688763-65-7
Elubrixin is a interleukin 8 inhibitor and CXCR2 selective antagonist, which is potentially useful for Inflammatory bowel disease therapies.
Baohuoside I Chemical Structure
BCP30977 Baohuoside I 113558-15-9
Baohuoside I, a flavonoid isolated from Epimedium koreanum Nakai, acts as an inhibitor of CXCR4, downregulates CXCR4 expression, induces apoptosis and shows anti-tumor activity.
ML339 Chemical Structure
BCP30789 ML339 2080300-49-6
ML-339 is a potent and selective hCXCR6 antagonist (IC50 = 140 nM).
MSX-130 Chemical Structure
BCP30792 MSX-130 4051-59-6
MSX-130 is CXCR4 Antagonist.
ATI-2341 Chemical Structure
BCP30749 ATI-2341 1337878-62-2
ATI-2341 is a CXCR4 agonist, induces CXCR4-dependent calcium flux, with an EC50 of 194 nM in CCRF-CEM cells. ATI-2341 is also a potent and efficacious mobilizer of bone marrow hematopoietic cells.
Repertaxin L-lysine salt Chemical Structure
BCP30625 Repertaxin L-lysine salt 266359-93-7
Reparixin is an inhibitor of CXCR1 and CXCR2 chemokine receptors. Functions as an agent that blocks a range of activities including leukocyte recruitment and IL-8 signaling.
Plerixafor Octahydrobromide Chemical Structure
BCP14117 Plerixafor Octahydrobromide 155148-32-6
VUF11207 Chemical Structure
BCP07780 VUF11207 1378524-41-4
VUF11207 is a highly potent CXCR7 agonist.
NSC-23026 Chemical Structure
BCP29974 NSC-23026 6616-56-4
NSC-23026, also known as MSX-127, is a CXCR4 receptor modulator.
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