RECHEM
Welcome to our website!|Hot Line: 86-21-61417495|E-mail: sales@rechemscience.com
Products Category
Contact Us
Tel: +86-21-61417495
Fax: +86-21-61417495
Email: sales@rechemscience.com
  info@rechemscience.com
QQ: 1369748377
Skype: sales@rechemscience.com
Home > Products > GPCR & G Protein
Cat.No. Product name Product Description
R10066 Dapagliflozin; BMS512148 Dapagliflozin is a potent and selective hSGLT2 inhibitor with EC50 of 1.1 nM, ex
R10123 Bosetan Bosentan is an endothelin (ET) receptor antagonist for ET-A and ET-B with Ki of
R10128 SRT3109 SRT3109 is a CXCR2 ligand for use in the treatment of chemokine mediated disease
R10132 Canagliflozin Canagliflozin is a highly potent and selective SGLT2 inhibitor for hSGLT2 with I
R10133 PF04971729; Ertugliflozin PF-04971729(Ertugliflozin) is a potent and selective inhibitor of the sodium-dep
R10185 CP945598 HCL Otenabant (CP-945598) HCl is a potent and selective cannabinoid receptor CB1 ant
R10186 CP945598 free base Otenabant (CP945598) is a recently discovered selective, high affinity, competit
R10242 AMG073 Cinacalcet HCl represents a new class of compounds for the treatment of hyperpar
R10260 Sotagliflozin; LP802034; LX4211 LX-4211 is a potent dual SGLT2/1 inhibitor; Antidiabetic agents.
R10406 AMD3465 hexahydrobromide AMD 3465 6HBr(GENZ-644494) is a potent, selective CXCR4 antagonist; exhibits 8-f
R10436 Ambrisentan; BSF208075; LU208075 Ambrisentan is a highly selective antagonist of the endothelin-1 type A receptor
R10488 Empagliflozin Empagliflozin (BI-10773) is a potent and selective SGLT-2 inhibitor with IC50 of
R10489 Canagliflozin hemihydrate Canagliflozin 0.5 H2O(JNJ 28431754; TA 7284) is a highly potent and selective SG
R10491 Ipragliflozin Ipragliflozin (ASP1941) is a highly potent and selective SGLT2 inhibitor with IC
R10492 Tofogliflozin Tofogliflozin(CSG-452) hydrate is a potent and highly specific sodium/glucose co
R10543 Plerixafor; AMD310 Plerixafor (AMD3100) is a chemokine receptor antagonist for CXCR4 and CXCL12-med
R10609 Reversine Reversine is a potent human A3 adenosine receptor antagonist with Ki of 0.66 μM,
R10725 CYM5442 CYM 5442 HCl is a potent and selective EDG-1 (S1P1) agonist in vitro (EC50 = 1.3
R10794 Capadenoson; BAY 68-4986 Capadenoson (BAY 68-4986) is a new adenosine A1 receptor agonist.
R10795 Preladenant; SCH420814 Preladenant (SCH 420814) is a potent and selective antagonist at the adenosine A
R10851 AM966 AM966 is a high affinity, selective, oral LPA1 (lysophosphatidic acid receptor,
R10848 Ki16198 Ki16198 is the methyl ester of Ki16425, which is a LPA antagonist and inhibits L
R10847 Ki16425 Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA
R10887 NPS-2143; SB 262470A NPS-2143 is a novel potent and selective antagonist of Ca(2+) receptor with IC50
R10950 ozanimod Ozanimod (RPC1063) is a selective oral S1P Receptor 1 modulator. Phase 3.
Page 1 / Total 2 FirstPrevNextLastGoto