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重点产品

编号化学名称Cas号纯度化学结构
92802SAG912545-86-999.03%
SAG is a potent Smoothened (Smo) receptor agonist (Kd = 59 nM); antagonizes Cyclopami
102703AZD-88351620576-64-8≧98.0%
AZD8835 is a potent and selective inhibitor ofPI3KαandPI3KδwithIC50s of 6.2 and 5.7
111013MGCD-265-analog875337-44-3≧98.0%
MGCD-265-analogis a tyrosine kinase inhibitor that selectively targets MET and Axl.MG
112101AV-412451492-95-899.38%
AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact
120103AGI-51981355326-35-098% 
AGI-5198 is a novel R132H-IDH1 inhibitor, identified through a high-throughput screen
122203Dalcetrapib211513-37-098% 
Dalcetrapib is a rhCETP inhibitor with IC50 of 0.2 M that increases the plasma HDL ch
122518SB-742457 ( Intepirdine )607742-69-898% 
SB-742457(Intepirdine) is a highly selective 5-HT6 receptor antagonist with pKi of 9.
122524GW2580870483-87-798% 
GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited huma
122805Balipodect ( TAK-063 ) 1238697-26-198% 
Balipodect (TAK 063 )is a novel PDE10A inhibitor. It has shown high inhibitory activi
122919Tenapanor1234423-95-098% 
Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein
122941Pacritinib(SB1518)937272-79-2≧98.0%
Pacritinib (SB1518) 是一种高选择性激酶抑制剂,对 JAK2、FLT3、IRAK1 和
1662118MK-8931 ( Verubecestat )1286770-55-598% by HPLC/HNMR 
MK-8931(verubecestat)是一种BACE抑制剂,是由默沙东公司研制开发。主