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Drug discovery based on the structure of FKBP12: Design, synthesis and evaluation of L-1,4-thiazane-3-carboxylic acid derivatives as neuroimmunophilin ligands
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作者 NIE AiHua XIAO JunHai +4 位作者 WANG LiLi LIAO GuoChao LIU HongYing REN Shen LI Song 《Science China Chemistry》 SCIE EI CAS 2007年第3期405-417,共13页
By choosing neuroimmunophilin FKBP12 as a therapeutical target, we have attempted to discover a new structural drug for treating neurodegenerative disease. This drug should possess neurotrophic activity and not affect... By choosing neuroimmunophilin FKBP12 as a therapeutical target, we have attempted to discover a new structural drug for treating neurodegenerative disease. This drug should possess neurotrophic activity and not affect the immune system. Based on the crystal structure of FKBP12, FK506 and Calcineurin complex, a series of small organic molecules were designed. These molecules were to have the ability of binding to FKBP12 in a virtual screening. By using a solution parallel synthetic method, these compounds were synthesized. The neuroprotective and neuroregenerative activities of these compounds were evaluated by binding assays, PC12 cells survival and neurite outgrowth model, chick dorsal root ganglion cultures (DRG) and 6-OHDA lesioned mice sympathetic nerve endings model. The evaluation results of these compounds showed that compound N308 has great promise as a candidate for a neuroprotective and neuroregenerative agent. 展开更多
关键词 FKBP12 L-1 4-thiazane-3-carboxylic acid derivatives DESIGN synthesis NEUROTROPHIC activity
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Synthesis of (2S,4S)-2-Substituted-3- (3-Sulfanylpropanoyl)-6- Oxohexahydropyrimidine-4-Carboxylic Acids as Potential Antihypertensive Drugs
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作者 Andrei Ershov Dmitry Nasledov +1 位作者 Igor Lagoda Valery Shamanin 《Journal of Materials Science and Chemical Engineering》 2015年第6期7-12,共6页
Proceeding from natural amino acid L-asparagine and commercially available aldehydes a stereoselective synthesis was developed of (2S,4S)-2-alkyl(aryl)-3-(3-sulfanylpropanoyl)-6-oxohexahy- dropyrimidine-4-carboxylic a... Proceeding from natural amino acid L-asparagine and commercially available aldehydes a stereoselective synthesis was developed of (2S,4S)-2-alkyl(aryl)-3-(3-sulfanylpropanoyl)-6-oxohexahy- dropyrimidine-4-carboxylic acids, potential antihypertensive drugs, inhibitors of the angiotensin converting enzyme. 展开更多
关键词 synthesis of (2S 4S)-2-Substituted-3- (3-Sulfanylpropanoyl)-6- Oxohexahydropyrimidine-4-carboxylic acidS AS POTENTIAL ANTIHYPERTENSIVE DRUGS
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Synthesis and Crystal Structure of a One-dimensional Infinite Chain Organotin Complex [(n-Bu)_3Sn(OCOC_5H_4NO)]_n 被引量:2
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作者 YIN Han-Dong GAO Zhong-Jun LI Gang XU Hao-Long HONG Min 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第11期1324-1327,共4页
A novel organotin complex [(n-Bu)3Sn(OCOC5H4NO)]n has been synthesized and characterized by elemental analysis, IR and ^1H NMR. The crystal structure has been determined by X-ray single-crystal diffraction. The cr... A novel organotin complex [(n-Bu)3Sn(OCOC5H4NO)]n has been synthesized and characterized by elemental analysis, IR and ^1H NMR. The crystal structure has been determined by X-ray single-crystal diffraction. The crystal belongs to monoclinic, space group P2 1/c with a = 8.982(2), b = 17.908(4), c = 13.219(3) A, β= 96.981(4)°, Z = 4, V= 2110.6(8) A^3, Dc = 1.347 g/cm^3, μ(MoKa) = 12.23 cm^-1, F(000) = 880, R = 0.0497 and wR = 0.1263. In the molecular structure of the title complex, the tin atoms are five-coordinated in a distorted trigonal bipyramidal geometry. A one-dimensional linear polymer is formed through an interaction between the O atoms of pyridine-3-carboxylic acid N-oxide and tin atoms of an adjacent molecule. 展开更多
关键词 organotin complex pyridine-3-carboxylic acid N-oxide synthesis crystal structure
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1H-吲唑-3-羧酸的合成 被引量:6
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作者 王燕 黄海洪 +1 位作者 饶尔昌 张曼云 《合成化学》 CAS CSCD 2005年第1期16-21,28,共7页
综述了1H-吲唑-3-羧酸的合成方法,并评述了其优缺点;同时介绍了作者在寻找其新合成方法中的一些探索。参考文献28篇。
关键词 1H-吲唑-3-羧酸 靛红 合成 综述
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1-氢吲唑-3-羧酸的合成 被引量:4
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作者 徐宝财 邓飞 杨建新 《广州化工》 CAS 2000年第4期108-108,98,共2页
以吲哚醌为原料,经碱催化开环、重氮化反应、还原反应及脱水环化制得1-氢吲唑 -3-羧酸,探讨了各因素对反应的影响,得到了较佳反应条件,收率达43%。
关键词 吲哚醌 氢吲唑羧酸 合成 药物中间体
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4-(3-氨基-2-羧基苯基)丁酸的合成
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作者 康从民 于国庆 《化学世界》 CAS CSCD 北大核心 2013年第2期97-99,117,共4页
4-(3-氨基-2-羧基苯基)丁酸是新型胸苷酸合成酶抑制剂的重要合成中间体。以3-(3-硝基苯甲酰基)丙酸乙酯为原料经过硝基还原、羰基还原、合环、开环等反应制得所需目标化合物。该方法具有生产成本低、反应条件温和、易于工业化生产的优点。
关键词 4-(3-氨基-2-羧基苯基)丁酸 合成 4-丁酸靛红 钯碳催化剂
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