Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
25001 | HC-5404 | 2247396-91-2 | ≧98.0% | |
HC-5404 is a novel, highly selective and potent PERK inhibitor. | ||||
24161 | CMP-5 2HCl | 2309409-79-6 | 98% Min. | |
CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit | ||||
24160 | Wu-5 | 2630378-05-9 | 98% Min. | |
Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de | ||||
24159 | VU-29 | 890764-36-0 | 98% Min. | |
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin | ||||
24158 | ML-202 | 1221186-52-2 | 98% Min. | |
ML-202 is an activator of pyruvate kinase M2 (PKM2). | ||||
24157 | BTA-EG4 hydrate | 921193-28-4 | 98% Min. | |
BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance | ||||
24156 | CYD19 | 2415281-52-4 | 98% Min. | |
CYD19 is a potent Snail/HDAC dual target inhibitor. | ||||
24155 | Phylloflavan | 98570-83-3 | 98% Min. | |
Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW | ||||
24154 | VK-28 | 312611-92-0 | 98% Min. | |
VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced | ||||
24153 | SR-11302 | 160162-42-5 | 98% Min. | |
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor. | ||||
24152 | AKOS037652256 | 2171065-77-1 | 98% Min. | |
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat | ||||
24151 | ML353 | 2990506-75-5 | 98% Min. | |
ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM). |
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