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Catalog NoChemical NameCAS NumberPurityChemical Structure
1811162PF-052310231037589-69-7>98%
PF-05231023 is a long-acting FGF21 mimetic. PF-05231023 decreases body weight and imp
17012102lumateperone(Tosylate)1187020-80-998%
Lumateperone (ITI-722/ITI-007) is a novel, first-in-class dual 5HT2A receptor antagon
S510901Cenicriviroc Mesylate497223-28-698% Min.
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che
S510902Cenicriviroc ( TAK-652 )497223-25-398% Min.
Cenicriviroc ( TAK-652, TBR-652) is an experimental drug candidate for the treatment
52105SNS-032 ( BMS-387032 )345627-80-798% 
SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
18722Fezolinetant1629229-37-3>98%
Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which
184321Ensartinib ( X396 )1370651-20-9>98%
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
512194Lazertinib1903008-80-998% Min.
Description:Lazertinib is a an orally available third-generation, selective inhibi
2623242-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane1350426-06-098% Min.
191146AR-9281913548-29-5>98%
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment
52026AMG-3191608125-21-898% 
AMG 319 is an investigational, highly selective, small molecule inhibitor of PI3K tha
2071401Pimodivir ( VX-787 )1629869-44-898% Min.
Pimodivir, also known as VX-787, JNJ-872, is a novel inhibitor of influenza virus rep