Cat.No. | Product Name | Information | Area |
---|---|---|---|
T4344 | ALW-II-41-27 | ALW-II-41-27, an Eph receptor tyrosine kinase inhibitor, is used for cancer therapy. | |
T4291 | (+)-Isocorydine hydrochloride | (+)-Isocorydine is a eukaryote protein kinases Inhibitor. | others |
T4257 | Belizatinib | Belizatinib is an effective, oral and dual inhibitor of ALK (IC50: 0.7?nM, wild-type ... | |
T3962 | TPI-1 | TPI-1 is a SHP-1 inhibitor. | |
T3569 | SU 5214 | SU 5214 is a modulator of tyrosine kinase signal transduction. | Others |
T3710 | XMD16-5 | XMD16-5 is a TNK2 inhibitor. TNK2 genomic amplification has been associated with late... | Cancer |
T3709 | XMD8-87 | XMD8-87 is a TNK2 inhibitor with activity in the inhibition of TNK2 phosphorylation. ... | Cancer |
T3160 | HUHS015 | HUHS015 is a potent PCA-1/ALKBH3 inhibitor. | Others |
T3312 | AM-2394 | AM-2394 is an effective and specific Glucokinase agonist (GKA, EC50: 60 nM), which ca... | Others |
T3403 | Glabridinnew | Glabridin may serve as an anti-inflammatory agent in diabetes-related vascular dysfun... | |
T3337 | Ddr1-In-1 | DDR1-IN-1 is an effective and specific?DDR1?receptor tyrosine kinase inhibitor (IC50:... | |
T3209 | AMG-337 | AMG-337 is an effective and highly specific ATP-competitive MET kinase inhibitor. ... |
Cancer |
T2709 | TAK901 | TAK-901 has been used in trials studying the treatment of Lymphoma, Myelofibrosis, Mu... | Cancer |
T2659 | GW 2580 | GW2580 is a specific, oral-bioavailable CSF-1R inhibitor for c-FMS. | Cancer |
T2457 | IRAK-1/4 Inhibitor | IRAK-1-4 Inhibitor I is a dual inhibitor of IRAK4 and IRAK1. | Cancer |
T2328 | Radotinib | Radotinib, and sometimes referred to by its investigational name IY5511, is a drug fo... | Cancer |
T2281 | GSK-2256098 | GSK-2256098 is a small molecule FAK kinase inhibitor. | Cancer |
T2153 | 1 nM-PP1 | 1 nM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor... | Cancer |
T2037 | TH588 | TH588 is nudix hydrolase family inhibitor that effectively and selectively engages an... | Cancer |
T2005 | TP0903 | TP-0903 is a potent and selective Axl kinase inhibitor. | Cancer |
T1991 | ZM 323881 hydrochloride | ZZZM 323881 hydrochloride is a potent and selective VEGFR2 inhibitor. | Other |
T1812 | KX1-004 | KX1-004, a potential protective drug for NIHL, is an effective small molecule inhibit... | Cancer |
T1803 | GNF-5 | GNF-5 is a specific non-ATP competitive inhibitor of Bcr-Abl (IC50: 0.22±0.1 uM, Wild... | Other |
T1606 | Fasudil | Fasudil is a potent inhibitor of ROCK1, PKA, PKC, and MLCK. | Nervous system |
T1527 | Gliclazide | Gliclazide, an oral antihyperglycemic agent, belongs to the sulfonylurea class of ins... | Metabolism system |
T1448L | Dasatinib monohydrate | Dasatinib is an orally bioavailable synthetic small molecule-inhibitor of SRC-family ... | Cancer |
T0979 | Dequalinium chloride | Dequalinium Chloride, a topical bacteriostat, is a selective blocker of apamin-sensit... | Respiratory system |
T6348 | NVP-BHG712 | NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates betwee... | others |