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首页 > 产品展示 > GPCR & G Protein
目录号 产品名称 产品描述
R10066 Dapagliflozin; BMS512148 Dapagliflozin is a potent and selective hSGLT2 inhibitor with EC50 of 1.1 nM, ex
R10067 EGT1442 EGT1442 is a potent and selective SGLT2 inhibitor.
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 Sotagliflozin (LX-4211) 是SGLT1/2抑制剂,是抗糖尿病剂。 
R10406 AMD3465 hexahydrobromide AMD 3465 6HBr(GENZ-644494) is a potent, selective CXCR4 antagonist; exhibits 8-f
R10436 Ambrisentan; BSF208075; LU208075 Ambrisentan 是一种选择性的ET A型受体 (ETAR) 拮抗剂。 
R10488 Empagliflozin Empagliflozin是一种选择性钠葡萄糖协同转运蛋白-2 (SGLT-2) 抑制剂,抑制人SGLT-2的IC50 为3.1 nM。 
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 是一种ATP-竞争性的 Aurora kinase 抑制剂,作用于 Aurora A,Aurora B 和 Aurora C,IC50 分别
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
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