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DI-87 Sale

目录号 : GC64342

DI-87 是一种具有口服活性的,选择性的脱氧胞苷激酶 (dCK) 抑制剂,EC50 为 10.2 nM。DI-87 具有抗肿瘤活性,可通过联合用药来抑制表达 dCK 的肿瘤。

DI-87 Chemical Structure

Cas No.:2107280-55-5

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1mg
¥1,980.00
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5mg
¥4,950.00
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Sample solution is provided at 25 µL, 10mM.

Description

DI-87 is an orally active and selective deoxycytidine kinase (dCK) inhibitor with an EC50 of 10.2 nM. DI-87 has antitumor activity and is used in combination therapy against tumors expressing dCK[1].

(S)-DI-87 exhibits a much higher IC50 value (IC50=468 nM) relative to DI-87 ((R)-DI-8) (IC50=3.15 nM) in CEM T-ALL cells for inhibition of dCK activity[1]. DI-87 (1 µM; for 72 hours) rescues human cell line CCRF-CEM (CEM) cells from the anti-proliferative effects of gemcitabine, a dCK-dependent nucleoside analog prodrug, with an EC50 of 10.2 nM[1].

DI-87 (5-25 mg/kg; oral gavage) exhibits full dCK inhibition for 27 hours, and enzyme activity fully recovered by 36 hours with 25 mg/kg dose[1]. DI-87 (10-50 mg/kg; oral) has plasma concentrations of between 1 and 3 hours and plasma half-life of 4 hours[1]. DI-87 (10 mg/kg/day or 25 mg/kg/twice a day; oral; for 16-18 days) with thymidine (2 g/kg; ip; twice a day) results in reduced tumor growth in male NSG mice implanted with CEM tumors[1].

[1]. Soumya Poddar, et al. Development and Preclinical Pharmacology of a Novel dCK Inhibitor, DI-87. Biochem Pharmacol. 2020 Feb;172:113742.

化学性质

Cas No. 2107280-55-5 SDF Download SDF
分子式 C23H30N6O3S2 分子量 502.65
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1 mg 5 mg 10 mg
1 mM 1.9895 mL 9.9473 mL 19.8946 mL
5 mM 0.3979 mL 1.9895 mL 3.9789 mL
10 mM 0.1989 mL 0.9947 mL 1.9895 mL
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