Sirpiglenastat(Synonyms: DRP-104)

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Sirpiglenastat (Synonyms: DRP-104)

Sirpiglenastat (DRP-104) 是一种广泛作用的谷氨酰胺 (glutamine) 拮抗剂。Sirpiglenastat通过直接靶向肿瘤代谢并同时诱导有效的抗肿瘤免疫反应而具有抗癌作用。

Sirpiglenastat(Synonyms: DRP-104)

Sirpiglenastat Chemical Structure

CAS No. : 2079939-05-0

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生物活性

Sirpiglenastat (DRP-104) is a broad acting glutamine antagonist. Sirpiglenastat has anticancer effects by directly targeting tumor metabolism and simultaneously inducing a potent antitumor immune response[1][2].

体外研究
(In Vitro)

Sirpiglenastat (DRP-104) treatment shows broad immune cell modulation effects including increased T, NK, and macrophages. Sirpiglenastat decreases pro-tumorigenic cytokines such as VEGF and KC (IL-8)[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

CT26 bearing mice treated with Sirpiglenastat (DRP-104) (0.5 mg/kg; s.c.; once a day; for 5 days) shows tumor growth inhibition at day 12 of 90%. Median survival days are 36 days[1].
Sirpiglenastat (0.5 mg/kg; s.c) treatment significantly inhibits tumor growth in the H22 model[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: CT26 bearing mice[1]
Dosage: 0.5 mg/kg
Administration: s.c.; once a day; for 5 days
Result: Showed tumor growth inhibition in mice.

分子量

441.48

Formula

C22H27N5O5

CAS 号

2079939-05-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Yumi Yokoyama, et al. DRP-104, a novel broad acting glutamine antagonist, induces distinctive immune modulation mechanisms and synergistic efficacy in combination with immune checkpoint blockade. J Immunother Cancer. 2019 Nov 6;7(Suppl 1):282.

    [2]. Yumi Yokoyama, et al. DRP-104, a broad acting glutamine antagonist, synergizes with immune checkpoint blockade in vivo. Cancer Res 2021;81(13_Suppl):Abstract nr 1563.

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