GDC-6036 (Synonyms: GDC-6036)
目录号: PL10861 纯度: ≥99%
CAS No. :2417987-45-0
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中文名称
GDC-6036
英文名称
GDC-6036
英文别名
1-((S)-4-((R)-7-(6-Amino-4-methyl-3-(trifluoromethyl)pyridin-2-yl)-6-chloro-8-fluoro-2-(((S)-1-methylpyrrolidin-2-yl)methoxy)quinazolin-4-yl)-3-methylpiperazin-1-yl)prop-2-en-1-one;Divarasib
Cas No.
2417987-45-0
分子式
C29H32ClF4N7O2
分子量
622.06
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
GDC-6036 是一种具有口服生物利用度,选择性的 KRAS G12C 抑制剂,IC50 为 <0.01 μM。GDC-6036 与 KRAS G12C 的开关 II (SW-II) 口袋共价结合,并将其不可逆地锁定在非活动的 GDP 结合状态。
生物活性
GDC-6036 is an orally bioavailable, highly potent, and selective KRAS G12C inhibitor with an IC 50 of <0.01 μM. GDC-6036 covalently binds to the switch II (SW-II) pocket of KRAS G12C and irreversibly locks it in the inactive GDP-bound state.
性状
Solid
IC50 & Target[1][2]
K-Ras(G12C) <0.01 μM (IC50)
体外研究(In Vitro)
GDC-6036 (compound 17a) has an EC50 of 2 nM in K-Ras G12C-alkylation HCC1171 cells has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
GDC-6036 (10-100 mg/kg/day; PO for 7 days) decreases the ratio of free KRAS G12C. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Female C.B-17 SCID (Inbred) mice (20-21 weeks old; 24
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Lingyao Meng, et al. Assessment of KRAS G12C Target Engagement by a Covalent Inhibitor in Tumor Biopsies Using an Ultra-Sensitive Immunoaffinity 2D-LC-MS/MS Approach. Anal Chem. 2022 Sep 20;94(37):12927-12933.
[2]. Sushant Malhotra, et al. Fused ring compounds. WO2020097537A2.
溶解度数据
In Vitro: DMSO : 100 mg/mL (160.76 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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