1632118-69-4 | BAR-501 (Catalog# : 179821)BAR-501 is a selective GPBAR1 agonist devoid of any FXR agonistic activity. BAR501 effectively reduced hepatic perfusion pressure and counteracted the vasoconstriction activity o
1207293-36-4 | BI-847325 (Catalog# : 83101)BI-847325 is an orally bioavailable, and selective dual MEK/Aurora kinase inhibitor with IC50 of 3 nM, 15 nM, 25 nM, and 4 nM for Xenopus laevis Aurora B, human Aurora A and Auro
1703793-34-3 | BLU-285 (Catalog# : 1781003)BLU-285 is a potent and selective inhibitor of PDGFR D842V and KIT Exon 17 mutants and is being developed as a highly targeted therapy for SM, a disorder of the mast cells in whi
1799753-84-6 | BAY-876 (Catalog# : 17030604)BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stability in vitro and high oral bioavailability in vivo. GLUT1 overexpression has been reported
1821496-27-8 | BDA-366 (Catalog# : 17030305)BDA-366 is a BCL2-BH4 antagonist. BDA-366 suppresses human myeloma growth. BDA-366 induces robust apoptosis in MM cell lines and primary MM cells by inducing BCL2 conformational
1909226-00-1 | BDA-366 (Catalog# : 16122769)BDA-366 is a small-molecule Bcl2-BH4 domain antagonist and binds BH4 with high affinity and selectivity.BDA-366 induces robust apoptosis in MM(Multiple myeloma) cell lines and pr
1257213-50-5 | BMS-986020 (Catalog# : 61122)BMS-986020 is a lysophosphatidic acid 1 receptor antagonist. BMS-986020 is in Phase 2 clinical development for treating idiopathic pulmonary fibrosis. BMS-986020 selectively inhi
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