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Rucaparib Camsylate

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产品价格:电议      采购度:1600      原产地:美洲

发布时间:2021/8/2 17:09:14      所属地区:上海 上海市

简要描述:

Rucaparib Camsylate 是 PARP 的抑制剂,对 PARP1 的 Ki 值为 nM。Rucaparib Camsylate 也可结合 PARP 其他八个结构域。

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Rucaparib Camsylate

CAS No. : 1859053-21-6

MCE 站:Rucaparib Camsylate

产品活性:Rucaparib Camsylate 是 PARP 的抑制剂,对 PARP1 的 Ki 值为 1.4 nM。Rucaparib Camsylate 也可结合 PARP 其他八个结构域。

研究领域:Cell Cycle/DNA Damage  |  Epigenetics

作用靶点:PARP

In Vitro: Rucaparib is the most potent PARP inhibitor in enzyme assays (Ki, 1.4 nM), and a possible N-demethylation metabolite of AG14644. The radio-sensitization by Rucaparib is due to downstream inhibition of activation of NF-κB, and is independent of SSB repair inhibition. Rucaparib could target NF-κB activated by DNA damage and overcome toxicity observed with classical NF-κB inhibitors without compromising other vital inflammatory functions. Rucaparib inhibits PARP-1 activity by 97.1% at a concentration of 1 μM in permeabilised D283Med cells.

In Vivo: Rucaparib and AG14584 significantly (P < 0.05) increases temozolomide toxicity. Rucaparib (1 mg/kg) significantly increases temozolomide-induced body weight loss. Rucaparib (0.1 mg/kg) results in a 50% increase in the temozolomide-induced tumor growth delay. Rucaparib is not toxic but significantly enhances temozolomide-induced TGD in the DNA repair protein-competent D384Med xenografts. Pharmacokinetics studies also show that Rucaparib is detected in the brain tissue, which indicates that Rucaparib has potential in intra-cranial malignancy therapy. Rucaparib significantly potentiates the cytotoxicity of topotecan and temozolomide in NB-1691, SH-SY-5Y, and SKNBE (2c) cells. Rucaparib enhances the antitumor activity of temozolomide and indicates complete and sustained tumor regression in NB1691 and SHSY5Y xenografts.

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更新时间:2024/1/2 10:17:29

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