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Catalog NoChemical NameCAS NumberPurityChemical Structure
20576STX-7212765525-82-2≧98.0%
STX-721 is a next-generation, orally delivered therapy, designed with potential best-
20639SOP1812 (QN-302)2546091-70-5≧98.0%
QN-302 is a G-quadruplex (G4)-selective transcription inhibitor.
20640FLAG-0031614235-14-1≧98.0%
FLAG-003 is a multi-acting, water-soluable small molecule therapeutic designed to tar
20641KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS )2082765-42-0≧98.0%
KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) is a small molecule inhibitor of protein
20642OATD-022146132-73-0≧98.0%
OATD-02, an orally available dual arginase inhibitor (ARG1 and ARG2), is in phase I c
262401MRTX17192630904-45-7≧96.0%
MRTX1719 is a potent and selective binder to the PRMT5•MTA complex and selectively
24004T-1095209746-59-8≧96.0%
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).
24008RNK-050472503036-46-0≧98.0%
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
24009Asengeprast (FT011)1001288-58-9≧98.0%
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
24010Zasocitinib2272904-53-5≧98.0%
Zasocitinib is under development for the treatment of moderate to severe plaque psori
24011Zongertinib2728667-27-2≧98.0%
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
24012Zunsemetinib1640282-42-3≧98.0%
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr