CAS: 17086-28-1; Doxycycline Monohydrate

该化合物是一种广泛频谱的抗生素,属于四环形,主要用于治疗各种细菌感染,包括呼吸道感染,尿道感染和某些皮肤状况,化学配方为C22H24N2O8SH2O,表明存在一种单水体,包括一种水分子;二氧环环环十二酸呈现一种黄色晶体外观,在水中溶解,适合口服和静脉注射;抑制细菌蛋白合成,从而阻止其生长和生殖,其物质寿命相对较长,允许在临床环境中每天服用一两次,而多氧环十二烷也因其抗炎特性而闻名,有时用于治疗丙烯和罗萨恰等情况;然而,必须指出,氧化环乙烷可引起光敏锐,在某些人群中应谨慎使用,例如孕妇和8岁以下儿童,因为可能对骨和牙齿发育产生影响.

结构式图片

欧盟法规

C&L通报REACH预注册

合成工艺路线路线简述

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    专利信息


    专利号:US-10968174-B2
    优先权日:2016-12-21
    标题:Synthesis of a thiosulfonic acid by a step of periodate mediated oxidative coupling of a thiosulfonic acid with an aniline
    发明人:SINCLAIR JAMES PETER; NICOLL SARAH LOUISE; STOREY JOHN MERVYN DAVID; LARCH CHRISTOPHER PAUL
    权利人:WISTA LAB LTD
    摘要:The present invention pertains generally to the field of chemical synthesis, and more particularly to methods for the chemical synthesis of a thiosulfonic acid of Formula (1) by a step of periodate mediated oxidative coupling of a thiosulfonic acid of Formula (2) with an aniline of Formula (3), as described herein. The present invention also relates to such methods which incorporate one or more additional (subsequent and/or preceding) steps, for example, to prepare compounds of Formula (5) from compounds of Formula (1); to prepare compounds of Formula (6) from compounds of Formula (5); and to prepare compounds of Formula (2) from compounds of Formula (4), as described herein.

    专利号:WO-2012047907-A9
    优先权日:2010-10-04
    标题 :Synthesis of c5-substituted tetracyclines, uses thereof, and intermediates thereto
    发明人:MYERS ANDREW G; WRIGHT PETER M; HECKER EVAN
    权利人:HARVARD COLLEGE; MYERS ANDREW G; WRIGHT PETER M; HECKER EVAN
    摘要:The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The recent development of a modular synthesis of tetracycline analogs through a chiral enone intermediate has allowed for the efficient synthesis of novel tetracycline analogs never prepared before. The present invention provides more efficient routes for preparing the enone intermediate and allows for a wide variety of substituents at position 5 of the tetracycline ring system.

    专利号:US-9688644-B2
    优先权日:2009-04-30
    标 题 :Synthesis of Tetracyclines and intermediates thereto
    发明人:MYERS ANDREW G; KUMMER DAVID A; LI DERUN; HECKER EVAN; DION AMELIE; WRIGHT PETER M
    权利人:HARVARD COLLEGE
    摘要:The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The recent development of a modular synthesis of tetracycline analogs through a chiral enone intermediate has allowed for the efficient synthesis of novel tetracycline analogs never prepared before. The present invention provides more efficient routes for preparing the enone intermediate and allows for substituents at positions 4a, 5, 5a, and 12a of the tetracycline ring system.

    专利号:US-9884830-B2
    优先权日:2004-05-21
    标题 :Synthesis of tetracyclines and analogues thereof
    发明人:MYERS ANDREW G; CHAREST MARK G; LERNER CHRISTIAN D; BRUBAKER JASON D; SIEGEL DIONICIO R
    权利人:HARVARD COLLEGE
    摘要:The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The modular synthesis of tetracyclines and tetracycline analogs described provides an efficient and enantioselective route to a variety of tetracycline analogs and polycyclines previously inaccessible via earlier tetracycline syntheses and semi-synthetic methods. These analogs may be used as anti-microbial agents or anti-proliferative agents in the treatment of diseases of humans or other animals.

    专利号:US-8907104-B2
    优先权日:2006-10-11
    标 题 :Synthesis of enone intermediate
    发明人:MYERS ANDREW G; BRUBAKER JASON D
    权利人:HARVARD COLLEGE
    摘要:The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The recent development of a modular synthesis of tetracycline analogs through a chiral enone intermediate has allowed for the efficient synthesis of novel tetracycline analogs never prepared before. The present invention provides a more efficient route for preparing the enone intermediate.

    专利号:US-2024197774-A1
    优先权日:2021-04-16
    标 题:Synthesis of Antimicrobial PVP-coated Bismuth Nanoparticles
    发明人:LOPEZ-RIBOT JOSE; VAZQUEZ-MUNOZ ROBERTO
    权利人:UNIV TEXAS
    摘要:Described herein is a facile, fast, and economical method for the synthesis of BAL-mediated PVP-BiNPs, using basic laboratory instruments and reagents readily available in most laboratories.
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    1: Ghasemi K, Ghasemi K. A Brief look at antitumor effects of doxycycline in the treatment of colorectal cancer and combination therapies. Eur J Pharmacol. 2021 Dec
    30:174593. doi: 10.1016/j.ejphar.2021.174593. Epub ahead of print. 14(3):102983. doi: 10.1016/j.arabjc.2020.102983. Epub 2021 Jan 10.
    3: Cárdenas Sierra RS, Zúñiga-Benítez H, Peñuela GA. Elimination of cephalexin and doxycycline under low frequency ultrasound. Ultrason Sonochem. 2021 Nov;79:105777. doi: 10.1016/j.ultsonch.2021.105777. Epub 2021 Oct 7.
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