Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
19132 | Cilofexor ( GS-9674 ) | 1418274-28-8 | ≧98.0% | |
Cilofexor (also known as GS-9674) is a nonsteroidal farnesoid X receptor (FXR) agonis | ||||
191122 | Tafenoquine ( WR 238605 ) | 106635-80-7 | ≧98.0% | |
Tafenoquine is being investigated as a potential treatment for malaria, as well as fo | ||||
191146 | AR-9281 | 913548-29-5 | >98% | |
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment | ||||
19356 | AZ876 | 898800-26-5 | >98% | |
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa | ||||
S510901 | Cenicriviroc Mesylate | 497223-28-6 | 98% Min. | |
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che | ||||
512193 | ITI-214(phosphate) | 1642303-38-5 | 98% Min. | |
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
52001 | Selisistat ( EX-527 ) | 49843-98-3 | ≧98.0% | |
Selisistatwas the first identified potent and cell permeable SIRT1-specific inhibitor | ||||
6111901 | UNC2541 | 1612782-86-1 | 98% Min. | |
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit | ||||
6111904 | Lemborexant (E-2006) | 1369764-02-2 | 98% Min. | |
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib | ||||
111891 | ONC206 | 1638178-87-6 | 98% Min. | |
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th | ||||
112191 | Aprocitentan | 1103522-45-7 | 98% Min. | |
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed | ||||
112591 | U-73343 | 142878-12-4 | 98% Min. | |
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p |
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