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_1421936-85-7.png "24084 | Iclepertin (BI-425809)")
_2408839-73-4.png "20636 | Edecesertib ( GS-5718 )")
_412003-95-3.png "2091204 | 5-hydroxy-2,4-dimethylpyrimidine")
RECOMMENDED PRODUCTSMORE >>
| Catalog No | Chemical Name | CAS Number | Purity |
|---|---|---|---|
| 41788 | CB-6644 CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL |
2316817-88-4 | 96.33% |
| 24068 | Acoramidis hydrochloride Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR |
2242751-53-5 | ≧98.0% |
| 24064 | Cirtuvivint Cirtuvivint is a CDC-like kinase (CLK) and dual-specificity tyrosine-phosphorylation- |
2143917-62-6 | ≧98.0% |
| 181121 | AZD-5904 AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590 |
618913-30-7 | ≧98.0% |
| 193264 | PF-06835919 ( MDK-1846 ) MDK1846 is a potent ketohexokinase (KHK) inhibitor. |
2102501-84-6 | ≧98.0% |
| 237071 | Flavopiridol ( Alvocidib ) Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst |
146426-40-6 | ≧98.0% |
| 24107 | LXH-3-71 LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH |
2251753-65-6 | ≧97.0% |
| 20509 | GLPG3667 GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development |
2308520-97-8 | ≧98.0% |
| 121431 | KW-2478 KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti |
819812-04-9 | 98% |
| 18576 | VU0467154 VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept |
1451993-15-9 | ≧98.0% |
| 171452 | BGB-15025 BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag |
2766481-17-6 | ≧98.0% |
| 17021601 | LY3039478 ( Crenigacestat ) LY3039478 ( Crenigacestat ), a selective NOTCH1 inhibitor, reduces intrahepatic chola |
1421438-81-4 | ≧98.0% |
| 711401 | Eganelisib ( IPI-549 ) Eganelisib (IPI-549) is a first-in-class, orally administered, highly selective PI3Kγ |
1693758-51-8 | ≧98.0% |
| 24067 | PBT434 Hydrobromide PBT434, also known as ATH434 , is a novel, brain-penetrant, inhibitor of α-synuclein |
1232841-78-9 | ≧98.0% |
| 233141 | NXP-800 ( CCT361814 ) NXP800 is an oral small molecule inhibitor of the Heat Shock Factor 1 (HSF1) pathway. |
1693734-80-3 | ≧98.0% |