Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
20576 | STX-721 | 2765525-82-2 | ≧98.0% | |
STX-721 is a next-generation, orally delivered therapy, designed with potential best- | ||||
20639 | SOP1812 (QN-302) | 2546091-70-5 | ≧98.0% | |
QN-302 is a G-quadruplex (G4)-selective transcription inhibitor. | ||||
20640 | FLAG-003 | 1614235-14-1 | ≧98.0% | |
FLAG-003 is a multi-acting, water-soluable small molecule therapeutic designed to tar | ||||
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 | ||||
24009 | Asengeprast (FT011) | 1001288-58-9 | ≧98.0% | |
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen | ||||
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 |
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