CAS: 4565-31-5; 5-Formylthiophene-2-Carboxylic Acid

该化合物是一种有机化合物,其特征是附于硫磷环的成型体组(CHO)和碳酸组(COOH),该化合物通常呈现黄色到浅褐色的表面,由于其功能组,在水和酒精等极地溶剂中可溶解.硫磷环的存在有助于其芳香特性,可能影响其再活性和稳定性.该化合物经常用于有机合成,特别是用于制作各种衍生物和开发制药及农用化学品.其再活性可归因于该成型组的电光性,使其在各种化学反应中成为有用的中间体.此外,该化合物可能展示出有趣的生物活动,尽管需要开展具体研究,以阐明其在药用化学中的潜在应用.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

5-甲基-2-噻吩甲酸 2-Methylthiophene-5-Carboxylic Acid 1918-79-2
5-醛基噻吩-2-甲酸甲酯 5-Formyl-Thiophene-2-Carboxylic Acid Methyl Ester 67808-64-4
2,5-噻吩二甲醛 2,5-Thiophenedicarboxaldehyde 932-95-6

合成工艺路线路线简述

    📜5-醛基噻吩-2-甲酸甲酯置于氢氧化钾,水体系中,用 四氢呋喃 作为反应溶剂,以59%的收率获得产物5-醛基-2-噻吩甲酸
    参考文献: 2-Substituted Heterocyclic Compounds And Antitumor Composition Comprising The Same[fr] Composes Heterocycliques Substitues En Position 2 Et Composition Antitumorale Renfermant Lesdits Composes
    标题: 2-Substituted Heterocyclic Compounds And Antitumor Composition Comprising The Same[fr] Composes Heterocycliques Substitues En Position 2 Et Composition Antitumorale Renfermant Lesdits Composes
    摘要:本发明涉及2-取代杂环化合物和包括其在内的抗肿瘤组合物.根据本发明的化合物基于新机制(端粒酶-端粒酶)表现出优越的端粒酶抑制剂效果,可以解决在使用化疗药物时出现的问题,即副作用和化疗药物之间相关机制的交叉耐药性.此外,包括本发明化合物的抗肿瘤组合物表现出优越的抑制癌细胞生长的效果.

    海关参考信息

    专利信息


    专利号:US-6090810-A
    优先权日:1995-09-01
    标题:Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities
    发明人:KLEIN ELLIOTT S; JOHNSON ALAN T; STANDEVEN ANDREW M; BEARD RICHARD L; GILLETT SAMUEL J; DUONG TIEN T; NAGPAL SUNIL; VULIGONDA VIDYASAGAR; TENG MIN; CHANDRARATNA ROSHANTHA A
    权利人:ALLERGAN SALES INC
    摘要:Aryl-substituted and aryl and (3-oxo-1-propenly)-substituted benzopyran, benzothiopyran, 1,2-dihydroquinoline, and 5,6-dihydronaphthalene derivatives have retinoid negative hormone and/or antagonist-like biological activities. The invented RAR antagonists can be administered to mammals, including humans, for the purpose of preventing or diminishing action of RAR agonists on the bound receptor sites. Specifically, the RAR agonists are administered or coadministered with retinoid drugs to prevent or ameliorate toxicity or side effects caused by retinoids or vitamin A or vitamin A precursors. The retinoid negative hormones can be used to potentiate the activities of other retinoids and nuclear receptor agonists. For example, the retinoid negative hormone called AGN 193109 effectively increased the effectiveness of other retinoids and steroid hormones in in vitro transactivation assays. Additionally, transactivation assays can be used to identify compounds having negative hormone activity. These assays are based on the ability of negative hormones to down-regulate the activity of chimeric retinoid receptors engineered to possess a constitutive transcription activator domain.

    专利号:US-5877207-A
    优先权日:1996-03-11
    标 题:Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities
    发明人:KLEIN ELLIOTT S; JOHNSON ALAN T; STANDEVEN ANDREW M; BEARD RICHARD L; GILLETT SAMUEL J; DUONG TIEN T; NAGPAL SUNIL; VULIGONDA VIDYASAGAR; TENG MIN; CHANDRARATNA ROSHANTHA A
    权利人:ALLERGAN SALES INC
    摘要:Aryl-substituted and aryl and (3-oxo-1-propenly)-substituted benzopyran, benzothiopyran, 1,2-dihydroquinoline, and 5,6-dihydronaphthalene derivatives have retinoid negative hormone and/or antagonist-like biological activities. The invented RAR antagonists can be administered to mammals, including humans, for the purpose of preventing or diminishing action of RAR agonists on the bound receptor sites. Specifically, the RAR agonists are administered or coadministered with retinoid drugs to prevent or ameliorate toxicity or side effects caused by retinoids or vitamin A or vitamin A precursors. The retinoid negative hormones can be used to potentiate the activities of other retinoids and nuclear receptor agonists. For example, the retinoid negative hormone called AGN 193109 effectively increased the effectiveness of other retinoids and steroid hormones in in vitro transactivation assays. Additionally, transactivation assays can be used to identify compounds having negative hormone activity. These assays are based on the ability of negative hormones to down-regulate the activity of chimeric retinoid receptors engineered to possess a constitutive transcription activator domain.

    专利号:US-2003219832-A1
    优先权日:1996-03-11
    标 题 :Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities
    发明人:KLEIN ELLIOTT S; STANDEVEN ANDREW M; NAGPAL SUNIL; CHANDRARATNA ROSHANTHA A
    摘要:Aryl-substituted and aryl and (3-oxo-1-propenly)-substituted benzopyran, benzothiopyran, 1,2-dihydroquinoline, and 5,6-dihydronaphthalene derivatives have retinoid negative hormone and/or antagonist-like biological activities. The invented RAR antagonists can be administered to mammals, including humans, for the purpose of preventing or diminishing action of RAR agonists on the bound receptor sites. Specifically, the RAR agonists are administered or coadministered with retinoid drugs to prevent or ameliorate toxicity or side effects caused by retinoids or vitamin A or vitamin A precursors. The retinoid negative hormones can be used to potentiate the activities of other retinoids and nuclear receptor agonists. For example, the retinoid negative hormone called AGN 193109 effectively increased the effectiveness of other retinoids and steroid hormones in in vitro transactivation assays. Additionally, transactivation assays can be used to identify compounds having negative hormone activity. These assays are based on the ability of negative hormones to down-regulate the activity of chimeric retinoid receptors engineered to possess a constitutive transcription activator domain.

    专利号:US-6469028-B1
    优先权日:1995-09-01
    标题:Synthesis and use of retinoid compounds having negative hormone and/or anatgonist activities
    发明人:KLEIN ELLIOTT S; JOHNSON ALAN T; STANDEVEN ANDREW M; BEARD RICHARD L; GILLETT SAMUEL J; DUONG TIEN T; NAGPAL SUNIL; VULIGONDA VIDYASAGAR; TENG MIN; CHANDRARATNA ROSHANTHA A
    权利人:ALLERGAN INC
    摘要:Aryl-substituted and aryl and (3-oxo-1-propenly)-substituted benzopyran, benzothiopyran, 1,2-dihydroquinoline, and 5,6-dihydronaphthalene derivatives have retinoid negative hormone and/or antagonist-like biological activities. The invented RAR antagonists can be administered to mammals, including humans, for the purpose of preventing or diminishing action of RAR agonists on the bound receptor sites. Specifically, the RAR agonists are administered or coadministered with retinoid drugs to prevent or ameliorate toxicity or side effects caused by retinoids or vitamin A or vitamin A precursors. The retinoid negative hormones can be used to potentiate the activities of other retinoids and nuclear receptor agonists. For example, the retinoid negative hormone called AGN 193109 effectively increased the effectiveness of other retinoids and steroid hormones in in vitro transactivation assays. Additionally, transactivation assays can be used to identify compounds having negative hormone activity. These assays are based on the ability of negative hormones to down-regulate the activity of chimeric retinoid receptors engineered to possess a constitutive transcription activator domain.

    专利号:US-5958954-A
    优先权日:1995-09-01
    标题 :Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities
    发明人:KLEIN ELLIOTT S; JOHNSON ALAN T; STANDEVEN ANDREW M; BEARD RICHARD L; GILLETT SAMUEL J; DUONG TIEN T; NAGPAL SUNIL; VULIGONDA VIDYASAGAR; TENG MIN; CHANDRARATNA ROSHANTHA A
    权利人:ALLERGAN SALES INC
    摘要:2,2-Dialkyl-4-aryl-substituted benzopyran and benzothiopyran derivatives of the formula where the symbols have the meaning described in the specification, have retinoid negative hormone and/or antagonist-like biological activities. The invented RAR antagonists can be administered to mammals, including humans, for the purpose of preventing or diminishing action of RAR agonists on the bound receptor sites. Specifically, the RAR agonists are administered or coadministered with retinoid drugs to prevent or ameliorate toxicity or side effects caused by retinoids or vitamin A or vitamin A precursors. The retinoid negative hormones can be used to potentiate the activities of other retinoids and nuclear receptor agonists.

    专利号:US-2002156054-A1
    优先权日:1995-09-01
    标题:Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Li, Y.; Fang, X.; Wang, Y., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 53.
    摘要:Li, Y.; Fang, X.; Wang, Y., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 24.
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