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Catalog NoChemical NameCAS NumberPurityChemical Structure
25197Bexobrutideg ( NX-5948 )2649400-34-8≧98.0%
Bexobrutideg (NX-5948) is a BTK degrader.
25198Bezuclastinib1616385-51-3≧98.0%
Bezuclastinib is an oral, small-molecule inhibitor of the kinase activity of the KIT
25199JX06729-46-4≧98.0%
JX06 is an effective, selective, covalent PDK inhibitor.
25194Oveporexton ( TAK-861 )2460722-04-5≧98.0%
Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
25201KL13331800405-30-4≧98.0%
KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
25202Flurpiridaz-Precursor863888-32-8≧98.0%
Flurpiridaz-Precursor in stock.
25204MAT2A inhibitor 52957874-18-7≧98.0%
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
25205AF710BN/A≧98.0% ; EE≧98.0%
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
25206MA242 TFA1049704-18-8≧98.0%
MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad
25207NSD1 inhibitor BT52351225-46-0≧98.0%
BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev
25208MK2562271348-04-8≧98.0%
MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg