Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
181121 | AZD-5904 | 618913-30-7 | ≧98.0% | |
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590 | ||||
171454 | 1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one | 1060810-24-3 | ≧98.0% | |
1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one, CAS 1060810-24-3. | ||||
20471 | FHD-286 | 2671128-05-3 | ≧98.0% | |
FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i | ||||
184163 | 2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile | 1032570-98-1 | >96% | |
2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile is a drug intermediate. | ||||
20657 | Zilurgisertib | 2173389-57-4 | ≧98.0% | |
Zilurgisertib (earlier known as INCB 00928) is an activin receptor-like kinase-2 (ALK | ||||
237071 | Flavopiridol ( Alvocidib ) | 146426-40-6 | ≧98.0% | |
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
20266 | Linzagolix | 935283-04-8 | ≧98.0% | |
Linzagolix is a novel, orally administered GnRH receptor antagonist that potentially | ||||
20510 | CC-92480 ( Mezigdomide ) | 2259648-80-9 | ≧98.0% | |
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno | ||||
20549 | STC-15 | 2648257-56-9 | ≧98.0% | |
STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me | ||||
51802 | TIC10 ( ONC201 ) | 1616632-77-9 | 99.85% | |
TIC10 ( ONC201 ), Bulk in stock, contact us by email for detailed quotation.ONC201/TI | ||||
23122601 | Navacaprant ( BTRX-335140 ) | 2244614-14-8 | ≧98.0% | |
Navacaprant (NMRA-335140, BTRX-140) is an oral, selective, reversible, small-molecule | ||||
20509 | GLPG3667 | 2308520-97-8 | ≧98.0% | |
GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development |
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