CAS: 53216-90-3; (1S,9S,11S,12E,14E,19Z,22R)-9,11-Dihydroxy-22-Methyl-6,23-Dioxa-26-Thia-2,17,27-Triazatricyclo[17.5.2.14,7]Heptacosa-4,7(27),12,14,19-Pentene-3,8,24-Trione

该化合物是一种天然化合物,被归类为多元抗生素,主要源自于某些真菌物种的发酵,特别是中的真菌,它具有抗风素特性,并被用于兽医,特别是动物的真菌感染的治疗;该化合物的特点是复杂的分子结构,包括多种共生的双重联系,有助于其生物活动;Griseoviridin以其通过干扰细胞过程抑制各种真菌生长的能力而著称;它经常用于研究,并被研究其对人类真菌感染治疗的潜在应用,尽管其在人类医学中的使用有限;此外,安全和毒性特征是重要的考虑因素,许多抗生素也是如此,而且在许多区域都对其使用进行管制.

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    专利信息


    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.

    专利号:CN-111676201-A
    优先权日:2020-06-30
    标 题:Asymmetric synthesis of stereoselective ketoreductase and (S)-3-hydroxybutyrate ethyl ester

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    合成参考文献


    摘要:Diver, S. T., Science of Synthesis, (2009) 46, 118.
    摘要:Antibiotics Annual., 2(790), 1954/1955
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