Asenapine maleate(Org 5222 maleate) inhibits adrenergic receptor (α1, α2A, α2B, α2C) with Ki of 0.25-1.2 nM and also inhibits 5-HT receptor (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) with Ki of 0.03-4.0 nM.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 10:14:21 ]
AT13387 is a synthetic, orally bioavailable, small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity. Hsp90 inhibitor AT13387 selectively binds to Hsp90, thereby inhibiting its chaperone function and promoting the degradation of oncogenic
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 10:10:11 ]
AT9283 is a small molecule a multi-targeted inhibitor with IC50s of 4, 1.2, 1.1 and approximate 3 nM for Bcr-Abl(T3151), JAK2 and JAK3, Aurora A and Aurora B, respectively.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 10:06:37 ]
AVL-292 is a covalent, highly selective, orally active small molecule inhibitor of Btk with IC50 value of 0.5 nM; >1400-fold selectivity over the other kinases assayed.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 10:01:57 ]
Axitinib is a multi-target inhibitor of VEGFR1 , VEGFR2 , VEGFR3 , PDGFRβ and c-Kit with IC50 of 0.1 nM, 0.2 nM, 0.1-0.3 nM, 1.6 nM and 1.7 nM in Porcine aorta endothelial cells, respectively.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:57:37 ]
LY2835219 is an orally available cyclin-dependent kinase (CDK) inhibitor that targets the CDK4 (cyclin D1) and CDK6 (cyclin D3) cell cycle pathway, with potential antineoplastic activity. LY2835219 specifically inhibits CDK4 and 6, thereby inhibiting retinoblastoma (Rb) protein p
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:51:30 ]
Nintedanib esylate (BIBF 1120 esylate) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50 of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:46:36 ]
ARRY-438162 (625 nM) inhibits in vitro osteoclast differentiation with IC50 of 39 nM. ARRY-438162 (10 μM) inhibits in vitro osteoclast resorption with IC50 of 625 nM. ARRY-438162 (2 μM) weakly affects osteoblast differentiation. ARRY-438162 is a recently disclosed potent and se
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:37:50 ]
BKM120 is a n orally bioavailable specific oral inhibitor of the pan-class I phosphatidylinositol 3 kinase (PI3K) family of lipid kinases with potential antineoplastic activity. Buparlisib specifically inhibits class I PIK3 in the PI3K/AKT kinase (or protein kinase B) signaling p
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:32:15 ]
Daclatasvir (BMS-790052; EBP 883) is a first-in-class, highly-selective oral HCV NS5A inhibitor. We do not have so much in stock right now. If you are in need of them, please hurry up.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:28:35 ]
Cabozantinib is a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-1/3/4, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM/11.3 nM/6 nM, 14.3 nM and 7 nM, respectively .
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:18:31 ]
Cabozantinib S-malate is a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-1/3/4, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM/11.3 nM/6 nM, 14.3 nM and 7 nM, respectively.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-03 09:14:30 ]
Cediranib (AZD2171) is a highly potent VEGFR(KDR) inhibitor with IC50 of <1 nM, also inhibits Flt1/4 with IC50 of 5 nM/≤3 nM, similar activity against c-Kit and PDGFRβ, 36-, 110-fold and >1000-fold selective more for VEGFR than PDGFR-α, CSF-1R and Flt3.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 15:00:50 ]
Cerdulatinib (PRT-062070) is an oral active, multi-targeted tyrosine kinase inhibitor with IC50 of 12 nM/6 nM/8 nM/0.5 nM and 32 nM for JAK1/JAK2/JAK3/TYK2 and Syk , respectively. Also inhibits 19 other tested kinases with IC50 less than 200 nM
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:58:25 ]
Chenodeoxycholic Acid (CDCA), is a hydrophobic primary bile acid that activates nuclear receptors(FXR) involved in cholesterol metabolism.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:55:33 ]
Coluracetam(MKC-231) is a new choline uptake enhancer.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:52:15 ]
Crizotinib is inhibitor of the c-Met kinase and the NPM-ALK.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:47:48 ]
Eletriptan hydrobromide is a orally active, selective 5-HT1B/1D receptor agonist Eletriptan hydrobromide produces a dose-dependent reduction in carotid artery blood flow in vivo. Displays antimigraine activity.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:44:43 ]
EMD 1214063 is a potent and selective c-Met inhibitor with IC50 of 4 nM, >200-fold selective for c-Met than IRAK4, TrkA, Axl, IRAK1, and Mer
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:41:33 ]
LGX818 is an orally available mutated BRaf V600E inhibitor(IC50=0.3 nM) with potential antineoplastic activity.
Shanghai Sun-shine bio-technology Co., Ltd [2015-06-02 14:38:51 ]
