CAS: 50-41-9; Clomiphene Citrate

该化合物是一种主要用于治疗妇女卵巢功能障碍的非类固醇生育药物,主要用于治疗妇女卵巢功能障碍,它作为一种选择性雌激素受体调节器(SERM),影响下脑-肾-脑-角形轴以刺激排卵. 克隆菌素的特点是它能够与雌激素受体结合,从而阻止雌激素在低脑上的负面反馈,从而导致从垂死腺中分离出更多的锥体激素(LH和FSH),这促进了卵巢卵巢受体发育和排卵.该物质通常通过口头施用,并因其相对较低的副作用而闻名.尽管它可能会造成热闪,情绪波动和卵巢超刺激等症状. 克隆菌素经常在周期中被规定,被认为是对因消食而患孕的妇女的第一线治疗. 它的化学结构包括一种独特的三乙基化学效果,它用于对抗生素的药物的药效,它具有独特的三基质性能,它用于对化学特性下的任何基质性能,它作为一种独特的药物的基质性能监测.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

2-{4-(1,2-diphenylethenyl)phenoxy}-N,N-diethylethanamine hydr°Chloride citric acid clomipheneclomiphene citrate cis-clomiphene citrate

合成工艺路线路线简述

    氯米芬,柠檬酸 以 乙醇 作为反应溶剂,化学反应 0.08H,以30.8 G的收率获得产物克罗米芬
    参考文献:一种恩氯米芬的制备方法
    标题:一种恩氯米芬的制备方法
    摘要:本发明涉及一种恩氯米芬的制备方法,包括:(1)克罗米芬或其盐,消旋联萘酚磷酸酯于含有醚类溶剂的醇类溶剂中反应,得到固体形式的恩氯米芬与联萘酚磷酸酯复合物;(2)将固体形式的恩氯米芬与联萘酚磷酸酯复合物经游离反应制得恩氯米芬.通过使用含有醚类溶剂的醇类溶剂作为拆分溶剂,恩氯米芬与拆分剂可形成固体复合物直接从拆分溶剂中析出,改善了反应体系的流动性,提供了一种拆分收率高,拆分产品纯度高,成本低,环境污染小,具有较好的工业应用前景的恩氯米芬的制备方法.

    海关参考信息

    专利信息


    专利号:US-9180171-B2
    优先权日:2011-01-25
    标题 :Method of regulating fertilizing ability using cyclic ADP-ribose and CD38
    发明人:KIM UH-HYUN; PARK KWANG-HYUN; KIM BYUNG-JU
    权利人:NAT UNIV CHONBUK IND COOP FOUND
    摘要:The present invention relates to a pharmaceutical composition for promoting fertilization comprising cyclic ADP-ribose or its derivative, CD38 and to a method of promoting fertilization by promoting the synthesis of cyclic ADP-ribose to increase sperm motility. Also, the present invention relates to a pharmaceutical composition for contraception and a method for inhibiting fertilization, which can inhibit the expression or function of cyclic ADP-ribose to reduce sperm motility, thereby inhibiting fertilization.

    专利号:US-2005053642-A1
    优先权日:2000-08-23
    标题:Biocompatible materials
    发明人:ULBRICHT MATHIAS; THOM VOLKMAR; JANKOVA KATJA; ALTANKOV GEORGE; JONSSON GUNNAR
    摘要:The present invention teaches a novel approach of creating biocmpatible surfaces, said surfaces being capable of functionally interact with biological material. SAid biocompatible surfaces comrise at least two comonents, such as a hydrophobic substratum and a macromolecule of hydrophilic nature, which, in a cooperativity, form together the novel biocoompatible surfaces. The novel approach is ased on contacting said hydrophobic substratum with a laterally patterned monomolecular layer of said hydrophilic and flexible macromolecules, exhibiting a pronounced excluded volume. The htus formed two component surface is, in respect to polarity and morphology, a molecularly heterogeneous surface. Structural features of said macromolecular monolayer (as e.g. the layer thickness or its lateral density) are determined by: i) the structural features of the layer forming macromolecules (as e.g. their MW or their molecular architecture) and ii) the method of creating said monomolecular layer (as e.g. by physi- or chemisorbing, or by chemically binding said macromolecules). The structural features of the layer forming macromolecules(s) is in turn determined by synthesis. AMount and conformation and thus also biological activity of biological material (as e.g. polypeptides) which contact the novel biocompatible surface, is determined and maintained by the cooperative action of the underlying hydrophobic substratum and the macromolecular layer. In this way it becomes possible to maintain and control biological interactions between said contacted polypeptides and other biological compounds as e.g. cells, antibodies and the like. Consequently, the present invention aims to reduce and/or eliminate the deactivation and/or denaturation associated with the contacting of polypeptides and/or other biological material to a hydrophobic substratum surface.

    专利号:US-6403576-B1
    优先权日:1998-08-24
    标题 :Antifungal and antiparasitic compounds
    发明人:JACKSON JOAN E; IWU MAURICE M; OKUNJI CHRISTOPHER O; BACCHI CYRUS; TALLY JR JOHN D; AYAFOR JOHNSON F
    权利人:US ARMY
    摘要:Novel antiparasitic and antifungal compositions are disclosed. The antiparasitic and antifungal compositions are useful for human and veterinary therapy for the treatment and/or prevention of parasitic infection. Also disclosed are novel mechanisms of identifying antifungal and antiparasitic compositions by their biochemical action on lipid synthesis and/or metabolism and/or excretion.

    专利号:PT-1883451-E
    优先权日:2005-04-13
    标 题 :SUBSTITUTED INDOOR COMPOUNDS WITH INHIBITORY ACTIVITY OF NITRIC OXIDE SYNTHESIS (NOS)
    北京海步国际医药科技发展有限公司
    ⚠️ 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.hopelife.cn
    电话: 86-10-67886402👤
    📞北京海步国际医药科技发展有限公司 ⚠️参考联系方式

    销售电话:86-10-67886402
    邮箱:apis@hopelife.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→

    ⚠️ 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。
    厦门志信化学有限公司
    ⚠️ 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.simagchem.com
    电话: 86 592 2680277👤
    📞厦门志信化学有限公司 ⚠️参考联系方式

    销售电话:86 592 2680277
    邮箱:sale@simagchem.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→

    ⚠️ 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。
    科菲医药有限公司
    ⚠️ 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.koffeepharm.com
    电话: 0086 (21) 6172-9394👤
    📞科菲医药有限公司 ⚠️参考联系方式

    销售电话:0086 (21) 6172-9394
    邮箱:sales01@koffeepharm.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→

    ⚠️ 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: El Refaeey A, Selem A, Badawy A. Combined coenzyme Q10 and clomiphene citrate for ovulation induction in clomiphene-citrate-resistant polycystic ovary syndrome. Reprod Biomed Online. 2014 Jul;29(1):119-24. doi: 10.1016/j.rbmo.2014.03.011. Epub 2014 Mar 26. doi: 10.1055/s-0033-1345271. Epub 2013 Jun 17. Review. doi: 10.1111/jog.12393. Review. doi: 10.1016/j.juro.2014.03.089. Epub 2014 Mar 21. doi: 10.1016/j.rbmo.2013.10.019. Epub 2013 Oct 31. doi: 10.1016/j.rbmo.2014.01.014. Epub 2014 Feb 8. doi: 10.1016/j.anireprosci.2014.07.019. Epub 2014 Jul 27. doi: 10.1016/j.fertnstert.2013.05.033. Epub 2013 Jun 27. doi: 10.1111/head.12491. Epub 2015 Mar 31. doi: 10.1007/s00404-012-2597-7. Epub 2012 Oct 19. doi: 10.1371/journal.pone.0108219. eCollection 2014.
    16: Xi W, Liu S, Mao H, Yang Y, Xue X, Lu X. Use of letrozole and clomiphene citrate combined with gonadotropins in clomiphene-resistant infertile women with polycystic ovary syndrome: a prospective study. Drug Des Devel Ther. 2015 Nov 11;9:6001-8. doi: 10.2147/DDDT.S83259. eCollection 2015.
    17: Niederberger C. Re: clomiphene citrate in the management of male infertility. J Urol. 2014 Mar;191(3):753. doi: 10.1016/j.juro.2013.11.072. Epub 2013 Dec 2. doi: 10.3109/09513590.2014.964640. Epub 2014 Sep 26. Polish. doi: 10.1002/14651858.CD002249.pub5. Review.

    合成参考文献


    参考文献:10.1186/1742-4755-3-5
    摘要:Perquin DA, de Craen AJ, Helmerhorst FM. Difficulties in recruitment for a randomized controlled trial involving hysterosalpingography. Reproductive Health. 2006 Jun 13;3(1):5. doi: 10.1186/1742-4755-3-5.
    参考文献:10.1007/s11096-011-9517-y
    摘要:Al-Riyami IM, Al-Busaidy IQ, Al-Zakwani IS. Medication use during pregnancy in Omani women. International Journal of Clinical Pharmacy. 2011 May 20;33(4):634–41. doi: 10.1007/s11096-011-9517-y.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知