CAS: 166671-26-7; 2-(2-Hydroxyethyl)-3-Methyl-1-Oxo-1,5-Dihydrobenzo[4,5]Imidazo[1,2-A]Pyridine-4-Carbonitrile

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714212-16-5 750599-25-8 121105-77-9

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CAS号517-23-7 2-乙酰基-γ-丁内酯 | CAS号4414-88-4 2-苯并咪唑基乙腈

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    📜α-乙酰基-γ-丁内酯,2-氰甲基苯并咪唑置于乙酸铵体系中,化学反应 1.0H,以90%的收率获得2-(2-羟基乙基)-3-甲基-1-氧代-1,5-二氢吡啶并[1,2-A]苯并咪唑-4-甲腈
    参考文献:Benzimidazole Condensed Ring System. Ix. Potential Antineoplastics. New Synthesis Of Some Pyrido[1,2-α]Benzimidazoles And Related Derivative
    标题:Benzimidazole Condensed Ring System. Ix. Potential Antineoplastics. New Synthesis Of Some Pyrido[1,2-α]Benzimidazoles And Related Derivative
    摘要:Some Pyrido[1,2-A]Benzimidazoles Were Prepared In Order To Investigate Their In Vitro Antineoplastic And Anti-Hiv Activities. Two Compounds (9B,Nsc 658526 And 15,Nsc 664715) Showed A Variable Degree Of Antineoplastic Activity Against Some Of The Cell Lines Tested. Compound 9A (Nsc 649900) Exhibited A Good In Vitro Antineoplastic Activity With Subpanel Disease Selectivity,Particularly Against Most Of The Cell Lines Of Leukemia And Some Cell Lines From Colon,Melanoma And Renal Cancer Panels.
    Doi:10.1016/0223-5234(96)88241-9

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    专利信息


    专利号:US-2005113397-A1
    优先权日:2002-01-31
    标题:Imidazo[1,2-a]pyridine derivative
    发明人:TAKEMURA MAKOTO; TAKAHASHI HISASHI; KAWAKAMI KATSUHIRO; TAKESHITA HIROSHI; KIMURA YOUICHI; WATANABE JUN; SUGIMOTO YUICHI; KITAMURA AKIHIRO; NAKAJIMA RYOHEI; KANAI KAZUO; FUJISAWA TETSUNORI
    摘要:A compound reprsented by the following formula (I), its salts or nsolvates thereof capable of specifically or selectively expressig an antifungal activity in a broad spectrum based on the novel mechanism thereof of 1,6-β-glucan synthesis inhibition, and an antifungal agent containing any of them.

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    合成参考文献


    参考文献:10.1016/j.bbrc.2023.08.050
    摘要:Ikeda Y, Davis MI, Sumita K, Zheng Y, Kofuji S, Sasaki M, Hirota Y, Pragani R, Shen M, Boxer MB, Takeuchi K, Senda T, Simeonov A, Sasaki AT. Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells. Biochemical and Biophysical Research Communications. 2023 Oct;679():116–21. doi: 10.1016/j.bbrc.2023.08.050.
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