CAS: 34707-92-1; Chlorothricin

该化合物是一个复杂的有机化合物,其特点是复杂的立体化学和多种功能组,其特征是一系列的氢氧(-OH)组,这些组有助于其溶性和反应,以及若干碳基(C=O)组表明在各种化学反应中具有反应性,例如核生殖器攻击中具有反作用的可能性,而使用甲氧糖表明它具有生物意义,有可能作为胶质旁或影响生物途径.氯化芳香运动表明它可能具有独特的电子特性,可能影响它与生物目标的相互作用.此外,(S)和(R)组合中标明的具体立体化学学表明,该化合物可能具有气质特性,影响其药用活动以及与酶或受体的相互作用,总体而言,该复合体的结构复杂性和功能多样性表明它有可能在药用化学中或药物开发中作为铅化合物.

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    CAS号157944-69-9

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      专利信息


      专利号:US-5399721-A
      优先权日:1990-01-12
      标题:Synthesis of optically pure 4-aryl-2-hydroxytetronic acids
      发明人:HOPPER ALLEN T; WITIAK DONALD T
      权利人:UNIV OHIO STATE RES FOUND
      摘要:The present invention relates to a method for synthesis of optically pure stereogenically labile 4-aryl-2-hydroxytetronic acids from an optically pure aldehyde. The invention further relates to the use of such optically pure compounds as potent inhibitors of platelet aggregation by working at the level of cyclooxygenase. the invention further relates to the pharmaceutical use of such compounds in the treatment of coronary artery diseases, especially in the treatment and/or prevention of atherosclerosis.

      专利号:US-5656662-A
      优先权日:1990-01-12
      标 题:Synthesis of optically pure 4-alkenyl- or 4-alkanyl-2-hydroxytetronic acids
      发明人:MANTRI PADMAJA; WITIAK DONALD T
      权利人:UNIV OHIO STATE RES FOUND
      摘要:The present invention relates to a method for synthesis of optically pure 4-alkenyl or 4-alkanyl-2-hydroxytetronic acids from an optically pure aldehyde. The invention further relates to the use of such optically pure compounds as potent inhibitors of platelet aggregation by working at the level of cyclooxygenase, thus making them useful in the treatment of coronary artery diseases, especially atherosclerosis, and additionally, as inhibitors of various inflammatory cytokines, making them useful in the treatment of both acute and chronic inflammation, as well in the treatment of cachexia, rheumatoid arthritis, multiple sclerosis, Crohn's disease and ulcerative colitis. The invention further relates to pharmaceutical compositions of the instant compounds.

      专利号:US-2008051323-A1
      优先权日:2004-08-21
      标 题 :Chloroquine drug compositions and methods for their synthesis
      发明人:KOSAK KENNETH M
      权利人:KOSAK KENNETH M
      摘要:This invention discloses compositions of chloroquine-coupled active agents, including methods for their preparation. The prior art has shown that chloroquines given as free drug in high enough concentration, enhances the release of various agents from cellular endosomes into the cytoplasm. The purpose of these compositions is to provide a controlled amount of chloroquine at the same site where the active agent is delivered, thereby reducing the overall dosage needed. n The compositions comprise a chloroquine substance coupled to an active agent directly or through a variety of pharmaceutical carrier substances. The carrier substances include polysaccharides, synthetic polymers, proteins, micelles and other substances for carrying and releasing the chloroquine compositions in the body for therapeutic effect. The compositions can also include a biocleavable linkage for carrying and releasing active agents for therapeutic or other medical uses. The invention also discloses carrier compositions that are coupled to targeting molecules for targeting the delivery of chloroquine substances and active agents to their site of action.

      专利号:US-2007060499-A1
      优先权日:2005-09-15
      标 题 :Chloroquine combination drugs and methods for their synthesis
      发明人:KOSAK KENNETH M
      权利人:KOSAK KENNETH M
      摘要:This invention discloses compositions of chloroquine-coupled active agents, including methods for their preparation. The prior art has shown that chloroquines given as free drug in high enough concentration, enhances the release of various agents from cellular endosomes into the cytoplasm. The purpose of these compositions is to provide a controlled amount of chloroquine at the same site where the active agent is delivered, thereby reducing the overall dosage needed. The compositions comprise a chloroquine substance coupled to an active agent directly or through a variety of pharmaceutical carrier substances. The carrier substances include polysaccharides, synthetic polymers, proteins, micelles and other substances for carrying and releasing the chloroquine compositions in the body for therapeutic effect. The compositions can also include a biocleavable linkage for carrying and releasing active agents for therapeutic or other medical uses. The invention also discloses carrier compositions that are coupled to targeting molecules for targeting the delivery of chloroquine substances and active agents to their site of action.

      专利号:US-2006040879-A1
      优先权日:2004-08-21
      标 题:Chloroquine coupled nucleic acids and methods for their synthesis
      发明人:KOSAK KENNETH M
      权利人:KOSAK KENNETH M
      摘要:This invention discloses compositions and methods for preparing chloroquine-coupled nucleic acid compositions. The prior art has shown that chloroquines given as free drug in high enough concentration, enhances the release of various agents from cellular endosomes into the cytoplasm. The purpose of these compositions is to provide a controlled amount of chloroquine at the same site where the nucleic acid needs to be released, thereby reducing the overall dosage needed. The compositions comprise a chloroquine substance coupled to a nucleic acid directly or through a variety of pharmaceutical carrier substances. The carrier substances include polysaccharides, synthetic polymers, proteins, micelles and other substances for carrying and releasing the chloroquine compositions in the body for therapeutic effect. The compositions can also include a biocleavable linkage for carrying and releasing nucleic acids for therapeutic or other medical uses. The invention also discloses nucleic acid carrier compositions that are coupled to targeting molecules for targeting the delivery of nucleic acids to their site of action.

      专利号:US-2005153913-A1
      优先权日:2001-04-10
      标 题 :Nucleic acid carrier compositions and methods for their synthesis
      发明人:KOSAK KENNETH M
      摘要:This invention discloses compositions and methods for preparing pharmaceutical nucleic acid carriers. The compositions comprise a carrier substance coupled to a nucleic acid intercalator whereby the intercalator is coupled by intercalation to the nucleic acid. The compositions can also include a biocleavable linkage for carrying and releasing nucleic acids for therapeutic or other medical uses. The invention also discloses nucleic acid carrier compositions that are coupled to targeting molecules for targeting the delivery of nucleic acids to their site of action.

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      合成参考文献


      参考文献:10.7164/antibiotics.39.1123
      摘要:Lee JJ, Lee JP, Keller PJ, Cottrell CE, Chang C, Zähner H, Floss HG. Further studies on the biosynthesis of chlorothricin. J Antibiot (Tokyo). 1986 Aug;39(8):1123–34. doi: 10.7164/antibiotics.39.1123.
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