Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
25052 | Lazertinib mesylate | 2247995-37-3 | ≧98.0% | ![]() |
Lazertinib is a an orally available third-generation, selective inhibitor of certain | ||||
25062 | GP130 modulator-1 | 2375779-31-8 | ≧98.0% | ![]() |
GP130 modulator-1 (compound A33) is agp130signaling pathway modulator. GP130 modulato | ||||
25063 | Seladelpar sodium salt | 3026272-26-1 | ≧98.0% | ![]() |
Seladelpar is a PPAR-delta agonist. | ||||
25065 | Ecopipam ( SCH 39166 ) | 112108-01-7 | ≧98.0% | ![]() |
Ecopipam ( SCH 39166 ) is a Selective Dopamine Receptor D1/D5 Antagonist used in the | ||||
25078 | CFT1946 | 2882165-79-7 | ≧98.0% | ![]() |
CFT1946 is an investigational, orally bioavailable small molecule degrader of BRAF V6 | ||||
24058 | NST-628 | 3002056-30-3 | ≧98.0% | ![]() |
NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and | ||||
25088 | Tonabersat ( SB-220453 ) | 175013-84-0 | ≧98.0% | ![]() |
Tonabersat, also known as SB-220453, is gap-junction modulator for the prevention of | ||||
25089 | Irpagratinib | 2230974-62-4 | ≧98.0% | ![]() |
Irpagratinib is an orally bioavailable, selective inhibitor of human fibroblast growt | ||||
25091 | Rilzabrutinib ( PRN1008 ) | 1575591-66-0 | ≧98.0% | ![]() |
Rilzabrutinib ( PRN1008 ) is an oral, reversible, covalent, small-molecule inhibitor | ||||
25094 | Nedisertib ( peposertib ) | 1637542-33-6 | ≧98.0% | ![]() |
Nedisertib, also known as M-3814, MSC2490484A, is an orally available inhibitor of DN | ||||
25095 | 5-Formyl-4-methyl-1H-indole-2-carbonitrile | 1857296-22-0 | ≧97.0% | ![]() |
25096 | 5-Iodo-4-methyl-1H-indole-2-carbonitrile | 3007670-38-1 | ≧97.0% | ![]() |
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