CAS: 36822-11-4; 2-Mercapto-6-Phenylpyrimidin-4-Ol

该化合物是一种化学化合物,属于硫酸盐类,是聚氨酯的衍生物,硫磺原子取代氧原子.该化合物的特征是,在聚氨酯环的6个位置上存在一个苯基组,这对其独特性能有帮助.该化合物一般看起来像白色的白色到白色的固体,有机溶剂中可溶解. 6-苯基-2-硫酸盐已经研究过,研究过它潜在的生物活动,包括其作为抗甲状腺剂的作用,因为它可以通过干扰将碘纳入甲状腺素中来抑制甲状腺激素的合成.此外,该化合物的结构可能表现出抗微生物和抗氟性.该化合物的结构允许与生物系统进行各种互动,从而引起对药用化学的兴趣.处理和接触安全数据应同任何化学物质一样用于处理和接触.

结构式图片

相似化合物

175202-77-4 375834-47-2 1239848-73-7

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

ammonium thi°Cyanate ethyl 3-oxo-3-phenylpropionate thiourea 5-benzoyl-2,2-dimethyl-1,3-dioxane-4,6-dione 2-methylthio-6-phenyl-3,4-dihydropyrimidin-4-one H-pyrimidine-2-thione6-phenyl-3,4-dihydro-1H-pyrimidine-2-thione 6-phenyluracil 6-phenylpyrimidine-2,4(1H,3H)-dithione

合成工艺路线路线简述

  • 合成目标产物 6-Phenyl-2-Thiouracil 主要起始原料 Methyl Benzoate
  • (文献来源)合成步骤主要原料 Methyl Benzoate
📜苯甲酸甲酯置于sodium Ethanolate,Sodium Hydride体系中,用 乙醇,甲苯,Mineral Oil 作为反应溶剂,化学反应 20.5H,反应生成 6-苯基-2-硫尿嘧啶
参考文献:Hts,然后进行基于NMR的反向筛选.发现和优化作为黄嘌呤氧化酶可逆和竞争性抑制剂的嘧啶酮
标题:Hts,然后进行基于NMR的反向筛选.发现和优化作为黄嘌呤氧化酶可逆和竞争性抑制剂的嘧啶酮
摘要:描述了新型,非嘌呤的黄嘌呤氧化酶抑制剂的鉴定.经过高通量筛选活动后,基于NMR的反筛选用于区分活性物,这些活性物以可逆方式与xo相互作用,与分析伪像分离.该方法将嘧啶酮1鉴定为可逆的竞争性抑制剂,具有非常好的铅样性质.导致先头运动获得化合物41,一种hxo的纳摩尔抑制剂,口服给药后在高尿酸血症大鼠模型中具有功效.
DOI:10.1016/j.Bmcl.2014.01.050

海关参考信息

专利信息


专利号:US-RE37623-E
优先权日:1993-11-02
标题:Enzyme inhibitors, their synthesis, and methods for use
发明人:EL KOUNI MAHMOUD H; NAGUIB FARDOS N M; SCHINAZI RAYMOND F
权利人:EL KOUNI MAHMOUD H; NAGUIB FARDOS N M; SCHINAZI RAYMOND F
摘要:Novel compounds are provided that are effective to inhibit the activity of DHUDase or UrdPase. Such compounds have the general formula n where X is S or Se; Y is H, I, F, Cl, Br, methoxy, benzyl, selenenylphenyl, or thiophenyl, and R 1 is H or an acyclo tail having the general formula n where R 2 is H, CH 2 OH or CH 2 NH 2 ; R 3 is OH, NH 2 , or OCOCH 2 CH 2 CO 2 H; and R 4 is O, S, or CH 2 . n The compounds can be used in pharmaceutical compositions, along with various chemotherapeutic agents to increase the efficacy of the treatment. These compounds can also be used in methods of treating patients by coadministering or sequentially administering the enzyme inhibiting compounds with a chemotherapeutic agent effective to treat cancers, or viral, fungal, bacterial, or parasitic infections. The compounds have further utility in enhancing imaging. Further, they can be administered alone to prevent and/or treat disorders of pyrimidine catabolism and other physiological disorders.

专利号:US-3890321-A
优先权日:1971-09-20
标题 :6-aryl-5-ethyl-pyrimidin-4-ol compounds useful as intermediates and bronchodilators
发明人:DEANGELIS GERALD GEORGE; HESS HANS-JURGEN ERNST
权利人:PFIZER
摘要:4-Hydroxy-5-ethyl-6-arylpyrimidines are useful intermediates leading to the synthesis of 4-amino-5-ethyl-6-arylpyrimidines, inhibitors of platelet aggregation and bronchodilators. 4Hydroxy-5-ethyl-6-phenylpyrimidine is also useful as a bronchodilator.

专利号:CN-108409635-A
优先权日:2018-05-10
标题:A kind of carbazole fluorescent thymine drug labeling reagent, synthesis and application

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: G Vargas, Et Al. Capillary Zone Electrophoresis Determination Of Thyreostatic Drugs In Urine. J Capillary Electrophor. 1998 Jan-Apr;5(1-2):9-12.
[参考文献]: Lei Zhang, Et Al. Simultaneous Determination Of Thyreostatic Residues In Animal Tissues By Matrix Solid-Phase Dispersion And Gas Chromatography-Mass Spectrometry. J Chromatogr A. 2005 May 13;1074(1-2):1-7.
[参考文献]: M Baba, Et Al. Highly Potent And Selective Inhibition Of Hiv-1 Replication By 6-Phenylthiouracil Derivatives. Antiviral Res. 1992 Apr;17(4):245-64.
[参考文献]: Marilyn J Schneider, Et Al. Validation Of A Streamlined Multiclass, Multiresidue Method For Determination Of Veterinary Drug Residues In Bovine Muscle By Liquid Chromatography-Tandem Mass Spectrometry. Anal Bioanal Chem. 2015 Jun;407(15):4423-35.
[参考文献]: R Schilt, Et Al. Screening And Confirmation Of Thyreostatics In Urine By Gas Chromatography With Nitrogen-Phosphorus Detection And Gas Chromatography-Mass Spectrometry After Sample Clean-Up With A Mercurated Affinity Column. J Chromatogr. 1989 Apr 7;489(1):127-37.

合成参考文献


摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 438.
摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 460.
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