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Catalog NoChemical NameCAS NumberPurityChemical Structure
20517HM432392569527-64-498% Min.
HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
20516(S)-3-AMINO-3-(4-CHLORO-PHENYL)-PROPIONIC ACID131690-60-398% Min.
205153-AMINO-3-(4-CHLOROPHENYL)PROPIONIC ACID19947-39-898% Min.
20511PDD40911373651-41-2≧98.0%
PDD4091 is a novel G6PD inhibitor.
20508AZD59912143061-81-6≧98.0%
AZD5991 is a potent and selective Mcl-1 inhibitor for treatment of hematologic cancer
1710901Netarsudil (AR-13324) 2HCl1253952-02-1≧98.0%
Netarsudil (a.k.a. AR-13324) is ROCK inhibitor with Ki value of 0.2-10.3 nM. It is cu
208191OATD-01 (GLPG-4716)2088453-21-6≧98.0%
OATD-01 (GLPG-4716), a dual inhibitor of acidic mammalian chitinase (AMCase) and chit
237071Flavopiridol ( Alvocidib )146426-40-6≧98.0%
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
2073108PF-06802861 ( ARRY 371797 ; ARRY-797 )1034189-82-6≧98.0%
ARRY 797 (also known as ARRY 371797 or PF 06802861) is an orally active, selective p3
011813Avoralstat918407-35-995.0% 
Avoralstat (formerly BCX4161) is a potent small-molecule oral plasma kallikrein inhib
20318Zotizalkib ( TPX-0131 )2648641-36-3≧98.0%
TPX-0131 is a next-generation ALK inhibitor drug candidate currently being evaluated
822221IACS-139092160546-07-4≧98.0%
IACS-13909 is a specific and potent allosteric inhibitor of SHP2, that suppresses sig