Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
611902 | PF-04979064 | 1220699-06-8 | ≧98.0% | ![]() |
PF-04979064 is a potent and selective PI3K/mTOR dual kinase inhibitor with an IC(50) | ||||
171680 | Bexotegrast ( PLN-74809 ) | 2376257-44-0 | ≧98.0% | ![]() |
Bexotegrast (Synonyms: PLN-74809) is a small-molecule, dual selective inhibitor of α | ||||
18435 | Ritlecitinib ( PF-06651600 ) | 1792180-81-4 | ≧98.0% | ![]() |
Ritlecitinib ( PF-06651600 ) is a potent and selective JAK3 inhibitor. PF-06651600, a | ||||
20318 | Zotizalkib ( TPX-0131 ) | 2648641-36-3 | ≧98.0% | ![]() |
TPX-0131 is a next-generation ALK inhibitor drug candidate currently being evaluated | ||||
20369 | Sunvozertinib ( DZD 9008 ) | 2370013-12-8 | ≧98.0% | ![]() |
Sunvozertinib, also known as DZD9008, is an oral, potent, irreversible, and selective | ||||
1711225 | Fosgonimeton (ATH-1017) | 2093305-05-4 | ≧98.0% | ![]() |
Fosgonimeton (ATH-1017) is a small molecule which enhance the activity of hepatocyte | ||||
171462 | MRTX0902 | 2654743-22-1 | ≧98.0% | ![]() |
MRTX0902is a potent SOS1 inhibitor which can be used for the therapeutic intervention | ||||
61726 | Ensifentrine ( RPL554 ) | 1884461-72-6 | ≧98.0% | ![]() |
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o | ||||
822221 | IACS-13909 | 2160546-07-4 | ≧98.0% | ![]() |
IACS-13909 is a specific and potent allosteric inhibitor of SHP2, that suppresses sig | ||||
232251 | Brepocitinib ( PF-06700841 ) | 1883299-62-4 | ≧98.0% | ![]() |
Brepocitinib is a potential first-in-class dual, selective inhibitor of TYK2 and JAK1 | ||||
20258 | CRT0273750 | 1979939-16-6 | ≧98.0% | ![]() |
CRT0273750 modulates LPA levels in plasma and is suitable for in vivo studies. | ||||
20376 | TOFA ( RMI14514; MDL14514) | 54857-86-2 | ≧98.0% | ![]() |
TOFA ( RMI14514; MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (A |
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