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Catalog NoChemical NameCAS NumberPurityChemical Structure
1711223Asciminib HCl2119669-71-3≧98.0%
Asciminib, also known as ABL001, is a potent allosteric inhibitor of BCR-ABL.
822221IACS-139092160546-07-4≧98.0%
IACS-13909 is a specific and potent allosteric inhibitor of SHP2, that suppresses sig
171462MRTX09022654743-22-1≧98.0%
MRTX0902is a potent SOS1 inhibitor which can be used for the therapeutic intervention
171652EZM04142411748-50-8≧98.0%
EZM0414 is a potent, selective, and orally bioavailable inhibitor of SETD2.
122622CNS004695205-24-4≧98.0%
CNS004 is a novel compound that potentiates NMDA receptor currents based on glutamate
52014NXY-059 ( Disufenton Sodium )168021-79-2≧98.0%
NXY-059 ( Disufenton Sodium ) is a disulfonyl derivative of phenyl-tert-butyl nitrone
232251Brepocitinib ( PF-06700841 )1883299-62-4≧98.0%
Brepocitinib is a potential first-in-class dual, selective inhibitor of TYK2 and JAK1
20460Ro5-333530195-30-3≧98.0%
Ro5-3335 is a lipophilic small molecule RUNX1 inhibitor.
233901RRX-001925206-65-1≧98.0%
RRx-001 is a highly selective NLRP3 inhibitor with vascular normalization and tumor a
20474Tinlarebant ( LBS-008 )1821327-95-0≧98.0%
Tinlarebant (LBS-008) is a small-molecule inhibitor of retinol binding protein 4 (RBP
230401Glycerol phenylbutyrate ( HPN-100 )611168-24-2≧98.0%
Glycerol phenylbutyrate, also known as HPN-100, is under trials in the treatment of c
232252Brepocitinib Tosylate2140301-96-6≧98.0%
Brepocitinib ( PF-06700841 ) is an orally available, selective inhibitor of non-recep