Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
24003 | NVL-655 ( ALK-IN-27 ) | 2739866-40-9 | ≧98.0% | |
NVL-655 is a novel, brain-penetrant, ALK-selective inhibitor that was designed to add | ||||
41788 | CB-6644 | 2316817-88-4 | 96.33% | |
CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
61726 | Ensifentrine ( RPL554 ) | 1884461-72-6 | ≧98.0% | |
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o | ||||
20513 | ZINC40099027 (ZN27) | 1211825-25-0 | ≧98.0% | |
ZINC40099027 (ZN27) is a specific focal adhesion kinase (FAK) activator that promotes | ||||
181121 | AZD-5904 | 618913-30-7 | ≧98.0% | |
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590 | ||||
237071 | Flavopiridol ( Alvocidib ) | 146426-40-6 | ≧98.0% | |
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
20510 | CC-92480 ( Mezigdomide ) | 2259648-80-9 | ≧98.0% | |
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno | ||||
20509 | GLPG3667 | 2308520-97-8 | ≧98.0% | |
GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development | ||||
121431 | KW-2478 | 819812-04-9 | 98% | |
KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti | ||||
18576 | VU0467154 | 1451993-15-9 | ≧98.0% | |
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept | ||||
171452 | BGB-15025 | 2766481-17-6 | ≧98.0% | |
BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag | ||||
17021601 | LY3039478 ( Crenigacestat ) | 1421438-81-4 | ≧98.0% | |
LY3039478 ( Crenigacestat ), a selective NOTCH1 inhibitor, reduces intrahepatic chola |
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