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Catalog NoChemical NameCAS NumberPurityChemical Structure
19132Cilofexor ( GS-9674 )1418274-28-8≧98.0%
Cilofexor (also known as GS-9674) is a nonsteroidal farnesoid X receptor (FXR) agonis
191122Tafenoquine ( WR 238605 )106635-80-7≧98.0%
Tafenoquine is being investigated as a potential treatment for malaria, as well as fo
191146AR-9281913548-29-5>98%
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment
19356AZ876898800-26-5>98%
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa
S510901Cenicriviroc Mesylate497223-28-698% Min.
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che
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