Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
20641 | KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) | 2082765-42-0 | ≧98.0% | |
KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) is a small molecule inhibitor of protein | ||||
20642 | OATD-02 | 2146132-73-0 | ≧98.0% | |
OATD-02, an orally available dual arginase inhibitor (ARG1 and ARG2), is in phase I c | ||||
262401 | MRTX1719 | 2630904-45-7 | ≧96.0% | |
MRTX1719 is a potent and selective binder to the PRMT5•MTA complex and selectively | ||||
24004 | T-1095 | 209746-59-8 | ≧96.0% | |
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs). | ||||
24008 | RNK-05047 | 2503036-46-0 | ≧98.0% | |
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi | ||||
24010 | Zasocitinib | 2272904-53-5 | ≧98.0% | |
Zasocitinib is under development for the treatment of moderate to severe plaque psori | ||||
24011 | Zongertinib | 2728667-27-2 | ≧98.0% | |
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit | ||||
24012 | Zunsemetinib | 1640282-42-3 | ≧98.0% | |
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr | ||||
24013 | Ziftomenib ( KO-539 ) | 2134675-36-6 | ≧98.0% | |
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th | ||||
24014 | Zelasudil | 2365193-22-0 | ≧98.0% | |
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho- |
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