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首页-小分子抑制剂&激动剂-Tyrosine Kinase-BTK-Rocbrutinib
Rocbrutinib

Chemical Structure : Rocbrutinib

CAS No.: 2485861-07-0

Rocbrutinib (LP-168, LP168)

货号: PC-23081Not For Human Use, Lab Use Only.

Rocbrutinib (LP-168) is a highly selective next-generation inhibitor of BTK that can bind wild-type BTK covalently and C481-mutated BTK non-covalently (reversibly), shows preclinical activity in resistant CLL models.

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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

Rocbrutinib (LP-168) is a highly selective next-generation inhibitor of BTK that can bind wild-type BTK covalently and C481-mutated BTK non-covalently (reversibly), shows preclinical activity in resistant CLL models.

物理化学性质&存储条件

分子量 761.93
分子式 C42H51N9O5
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-[5-[[6-[2-(1,3,4,6,7,8-Hexahydro-7,7-dimethyl-1-oxo-2H-cyclopenta[4,5]pyrrolo[1,2-a]pyrazin-2-yl)-3-(hydroxymethyl)-4-pyridinyl]-3,4-dihydro-4-methyl-3-oxo-2-pyrazinyl]amino]-2-[(2S)-2-methyl-4-(tetrahydro-2H-pyran-4-yl)-1-piperazinyl]phenyl]-2-propenamide

参考文献

1. Patent WO2020176403 A1.

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