CAS: 58546-54-6; (6S,7S,13Ar)-1,2,3,13-Tetramethoxy-6,7-Dimethyl-5,6,7,8-Tetrahydrobenzo[3',4']Cycloocta[1',2':4,5]Benzo[1,2-D][1,3]Dioxol-6-Ol

该化合物是一种天然化合物,主要来自Schisandra中国人植物的产物,通常以传统医药用途闻名,其特点是复杂的多环结构,有助于生物活动;Gomisin A展示了各种药理特性,包括抗氧化剂,抗炎和肝脏保护效应,使其对传统医学和现代药理都感兴趣;该化合物是研究其潜在的...

结构式图片

欧盟法规

C&L通报

上下游产品

CAS号72551-73-6 met B | CAS号74-95-3 二溴甲烷 | CAS号143552-03-8 ((2'R,7S)-1,2,3... | CAS号86-81-7 3,4,5-三甲氧基苯甲醛 | CAS号143616-17-5 (S)-(E)-3-[5-Me... | CAS号143503-88-2 4-(3,4-dihydrox...

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:WO-9421230-A1
    优先权日:1993-03-19
    标题 :Method and compositions for disrupting the epithelial barrier function
    发明人:ELIAS PETER M; THORNFELDT CARL R; GRAYSON STEPHEN
    权利人:CELLEGY PHARMA INC; UNIV CALIFORNIA; ELIAS PETER M; THORNFELDT CARL R; GRAYSON STEPHEN
    摘要:A method for disrupting epithelial barrier function in a host in need of the topical administration of a physiologically active substance which comprises applying to the epithelium of the host, barrier-disrupting amount of at least one agent selected from the group consisting of an inhibitor of ceramide synthesis, inhibitor of acylceramide synthesis, inhibitor of glucosylceramide synthesis, and inhibitor of sphingomyelin synthesis, an inhibitor of fatty acid synthesis, an inhibitor of cholesterol synthesis, a degradation enzyme of ceramides, acylceramide, glucosylceramides, sphingomyelin, an inhibitor of phospholipid, glycosphingolipid, including glucosylceramide, acylceramide or sphingomyelin degradation, and both inhibitors and stimulators of metabolic enzymes of free fatty acids, ceramide, and cholesterol, as well as a topical composition useful therefor are disclosed.

    专利号:WO-9817253-A1
    优先权日:1996-10-23
    标 题 :Method and compositions for disrupting the epithelial barrier function
    发明人:ELIAS PETER M; FEINGOLD KENNETH R; HOLLERAN WALTER M; THORNFELDT CARL R
    权利人:UNIV CALIFORNIA; CELLEGY PHARMA INC
    摘要:A method for disrupting epithelial barrier function in a host in need of the topical administration of a physiologically active substance which comprises applying to the epithelium of the host, barrier-disrupting amount of at least one agent selected from the group consisting of an inhibitor of ceramide synthesis, inhibitor of acylceramide synthesis, inhibitor of glucosylceramide synthesis, and inhibitor of sphingomyelin synthesis, an inhibitor of fatty acid synthesis, an inhibitor of cholesterol synthesis, a degradation enzyme of ceramides, acylceramide, glucosylceramides, sphingomyelin, an inhibitor of phospholipid, glycosphingolipid, including glucosylceramide, acylceramide or sphingomyelin degradation, and both inhibitors and stimulators of metabolic enzymes of free fatty acids, ceramide, and cholesterol, as well as a topical composition useful therefor are disclosed.

    专利号:US-6562606-B1
    优先权日:1993-03-19
    标 题:Methods and compositions for disrupting the epithelial barrier function
    发明人:ELIAS PETER M; FEINGOLD KENNETH R; HOLLERAN WALTER M
    权利人:UNIV CALIFORNIA; CELLEGY PHARMA INC
    摘要:A method for disrupting epithelial barrier function in a host in need of the topical administration of a physiologically active substance which comprises applying to the epithelium of the host, barrier-disrupting amount of at least one agent selected from the group consisting of an inhibitor of ceramide synthesis, inhibitor of acylceramide synthesis, inhibitor of glucosylceramide synthesis, and inhibitor of sphingomyelin synthesis, an inhibitor of fatty acid synthesis, an inhibitor of cholesterol synthesis, a degradation enzyme of ceramides, acylceramide, glucosylceramides, sphingomyelin, an inhibitor of phospholipid, glycosphingolipid, including glucosylceramide, acylceramide or sphingomyelin degradation, and both inhibitors and stimulators of metabolic enzymes of free fatty acids, ceramide, and cholesterol, as well as a topical composition useful therefor are disclosed.
    西安金瑞国际贸易有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.jinruigroup.com
    电话: 0086-29-88490350 / +86-29-87361679👤
    📞西安金瑞国际贸易有限公司 ⚠️参考联系方式

    销售电话:0086-29-88490350 / +86-29-87361679
    邮箱:info@jinruigroup.com
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:陕西省西安市新城区尚朴路南长巷10号
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    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


    1: Liang H, Li XY, Zhang XW, Bao YW, Ding ML, Yuan QH, He CS, Zeng N. [Mechanism of Ganke Granules intervening acute lung injury based on network pharmacology and experimental verification]. Zhongguo Zhong Yao Za Zhi. 2024 Apr;49(8):2197-2209. Chinese. doi: 10.19540/j.cnki.cjcmm.20240115.706.

    合成参考文献


    参考文献:10.5281/zenodo.5794106
    摘要:The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata) | DOI:10.5281/zenodo.5794106
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知