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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
24001Bomedemstat1990504-34-1≧98.0%
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
20620Brexpiprazole913611-97-998% Min.
Brexpiprazole, also known as OPC-34712, is a novel D2 dopamine partial agonist called
20619Berotralstat HCl1809010-52-398% Min.
Berotralstat HCl is a novel selective inhibitor of plasma kallikrein, blocking the en
20606Belzutifan1672668-24-498% Min.
Belzutifan, also known as PT2977 and MK-6482, is HIF-2alpha inhibitor. PT2977 binds t
20601BI-1467335 HCl1478364-68-998% Min.
BI-1467335, also known as PXS-4728A, is a SSAO/VAP inhibitor potentially for the trea
20599Bozitinib1440964-89-598% Min.
Bozitinib is a highly selective c-MET kinase inhibitor with blood-brain barrier perme
20597BMS-9861761815613-42-398% Min.
BMS-986176, also known as LX9211, is a highly selective, CNS penetrant, potent AAK1 i
20570BBT445000-45-398% Min.
BBT is an enhancer of impaired glucose-stimulated insulin secretion (GSIS).
205641,1'-Biphenyl, 2-iodo-2113-51-198% Min.
1,1'-Biphenyl, 2-iodo- is a biochemical.
20554BML-278120533-76-898% Min.
BML-278 is an activator of sirtuin 1 (SIRT1) that has an EC150 value (effective conce
20550BSJ-04-1222513289-74-098% Min.
20533brigimadlin2095116-40-698% Min.
Brigimadlin is an E3 ubiquitin-protein ligase Mdm2 inhibitor with potential as an ant
20519BMS-9861201478712-37-698% Min.
BMS-986120 is a potent and selective oral antagonist of protease-activated receptor-4
20518BMS-9861411478711-48-698% Min.
BMS-986141 is an Orally-Active Small-Molecule Antagonist of the Platelet Protease-Act
20512BDTX-15352607829-38-7≧98.0%
BDTX-1535 is a brain-penetrant and potent MasterKey inhibitor of oncogenic mutations
232252Brepocitinib Tosylate2140301-96-6≧98.0%
Brepocitinib ( PF-06700841 ) is an orally available, selective inhibitor of non-recep
20496BRD4 degrader AT12098836-45-298% Min.
BRD4 degrader AT1 is an analogue of MZ1. It shows improved selectivity for BRD4 degra
20492BJJF0782531244-56-998% Min.
BJJF078 is a potent inhibitor of recombinant human and mouse Transglutaminase enzyme
20485BRD06392760881-74-998% Min.
BRD0639 is a potent PRMT5 inhibitor. BRD0639 engages the target in cells, disrupts PR
230402BI 1015550 ( Nerandomilast )1423719-30-5≧98.0%
BI 1015550 ( Nerandomilast )is an oral, preferential inhibitor of phosphodiesterase 4
20469BT44924759-42-298% Min.
BT44 is a novel RET agonist for the treatment of experimental neuropathies.
232251Brepocitinib ( PF-06700841 )1883299-62-4≧98.0%
Brepocitinib is a potential first-in-class dual, selective inhibitor of TYK2 and JAK1
20453BIIB0681798787-27-598% Min.
20451Baxdrostat1428652-17-898% Min.
Baxdrostat is an aldosterone synthase inhibitor.
20445BMS-9862512114324-48-898% Min.
20444BMS-9861951912445 -55-698% Min.
20428Branebrutinib1912445-55-698% Min.
Branebrutinib, also known as BMS-986195, is a potent, covalent, irreversible inhibito
171680Bexotegrast ( PLN-74809 )2376257-44-0≧98.0%
Bexotegrast (Synonyms: PLN-74809) is a small-molecule, dual selective inhibitor of α
1716534-Bromo-6-methylpyridine-2-carbonitrile886372-53-8≧95.0%
4-Bromo-6-methylpyridine-2-carbonitrile, CAS 886372-53-8
1714541-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one1060810-24-3≧98.0%
1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one, CAS 1060810-24-3.