Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
24017 | AMG-193 | 2790567-82-5 | 98.62%; EE 98.28% | |
AMG-193 is an oral, small-molecule, methylthioadenosine-cooperative inhibitor of the | ||||
41788 | CB-6644 | 2316817-88-4 | 96.33% | |
CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
24068 | Acoramidis hydrochloride | 2242751-53-5 | ≧98.0% | |
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR | ||||
24064 | Cirtuvivint | 2143917-62-6 | ≧98.0% | |
Cirtuvivint is a CDC-like kinase (CLK) and dual-specificity tyrosine-phosphorylation- | ||||
181121 | AZD-5904 | 618913-30-7 | ≧98.0% | |
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590 | ||||
237071 | Flavopiridol ( Alvocidib ) | 146426-40-6 | ≧98.0% | |
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst | ||||
24107 | LXH-3-71 | 2251753-65-6 | ≧97.0% | |
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH | ||||
20509 | GLPG3667 | 2308520-97-8 | ≧98.0% | |
GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development | ||||
121431 | KW-2478 | 819812-04-9 | 98% | |
KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti | ||||
18576 | VU0467154 | 1451993-15-9 | ≧98.0% | |
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept | ||||
171452 | BGB-15025 | 2766481-17-6 | ≧98.0% | |
BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag | ||||
17021601 | LY3039478 ( Crenigacestat ) | 1421438-81-4 | ≧98.0% | |
LY3039478 ( Crenigacestat ), a selective NOTCH1 inhibitor, reduces intrahepatic chola |
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