| Identification | Back Directory | [Name]
1,2,4-Triazolo[4,3-a]pyrazin-8-amine, N,3-dimethyl-6-[6-(4-methyl-1-piperazinyl)-1-(phenylmethyl)-1H-benzimidazol-2-yl]- | [CAS]
1610044-98-8 | [Synonyms]
Amredobresib
3-a]pyrazin-8-amine
3-dimethyl-6-[6-(4-methyl-1-piperazinyl)-1-(phenylmethyl)-1H-benzimidazol-2-yl]-
1,2,4-Triazolo[4,3-a]pyrazin-8-amine, N,3-dimethyl-6-[6-(4-methyl-1-piperazinyl)-1-(phenylmethyl)-1H-benzimidazol-2-yl]- | [Molecular Formula]
C26H29N9 | [MOL File]
1610044-98-8.mol | [Molecular Weight]
467.57 |
| Chemical Properties | Back Directory | [density ]
1.36±0.1 g/cm3(Predicted) | [storage temp. ]
4°C, away from moisture and light | [form ]
Solid | [pka]
7.70±0.42(Predicted) | [color ]
Light yellow to yellow |
| Hazard Information | Back Directory | [Uses]
Amredobresib is a potent inhibitor of BET. Amredobresib inhibits the binding of bromodomains to acetylated lysines on histone H3 and H4 and thus acts as important regulators of gene transcription. Amredobresib is useful for the research of acute myeloid leukemia (AML) and cancer (extracted from patent WO2019145410A1 and WO2021175824A1)[1]. | [References]
[1] Ulrike Tontsch-Grunt, et al. Combination treatment of acute myeloid leukemia. Patent WO2019145410A1.
[2] Shaonan Wang, et al. Method for administration of an anti cancer agent. Patent WO2021175824A1. |
|
| Company Name: |
BOC Sciences
|
| Tel: |
1-631-485-4226; 16314854226 |
| Website: |
https://www.bocsci.com |
|