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Catalog NoChemical NameCAS NumberPurityChemical Structure
512193ITI-214(phosphate)1642303-38-598% Min.
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
52001Selisistat ( EX-527 )49843-98-3≧98.0%
Selisistatwas the first identified potent and cell permeable SIRT1-specific inhibitor
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
6111904Lemborexant (E-2006)1369764-02-298% Min.
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib
111891ONC2061638178-87-698% Min.
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th
112191Aprocitentan1103522-45-798% Min.
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
112591U-73343142878-12-498% Min.
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
203071CC-900091860875-51-998%
CC-90009 is a modulator of cereblon (CRBN), which is part of the cullin 4-RING E3 ubi
204302Lerociclib1628256-23-4 (free base)98%
Lerociclib , also known as G1T38, is an oral, potent and selective CDK4/6 inhibitor f
204305ICEC0942 HCl1805789-54-1 (HCl)98% Min.
ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
204504Zegocractin ( CM-4620 )1713240-67-5≧98.0%
Zegocractin (CM-4620, Auxora(TM)) is a small-molecule inhibitor of the calcium releas
2041232-oxo-5,5-diphenyltetrahydro-4-furancarboxylic acid79371-39-4≧96.0%