CAS: 514-36-3; Fludrocortisone Acetate

该化合物是一种合成的花生类动物,具有抗炎和矿物类动物特性,主要用于治疗肾上腺不适和孔地性低温等条件,其特点是能够提高肾中的钠保留量和钾排泄量,这有助于调节血液压力和液体平衡;该化合物通常通过口服施用,以其相对较高的能力而闻名于其他花生类.氟甲酸酯的乙酸酯有一个分子配方,反映其血清结构,其特点是循环开球多氢苯丙胺核心,这是气候性固醇中常见的,其药理效应通过激活矿物类受体的感应器进行介介介,导致各种生理反应.该物质一般都受到很好的调控,但潜在的副作用可能包括高血压,低血糖和液体保留,在治疗期间需要谨慎监测.与所有花生类固醇的微生物一样,它有效地管理了对降低水分的有害作用.

结构式图片

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上下游产品

CAS号4383-30-6 21-乙酰氧基-9Β,11Β-... | CAS号566-35-8 11-表氢化可的松 | CAS号7753-60-8 δ-9(11)-氢化可的松醋酸酯 | CAS号50733-54-5 9-Bromo-11,17,2... | CAS号113862-93-4 21-Acetoxy-17α-... | CAS号67-66-3 氯仿 | CAS号7664-39-3 氟化氢 | CAS号338-98-7 醋酸异氟泼尼松 | CAS号338-95-4 异氟泼尼松 | CAS号127-31-1 氟氢可的松

合成工艺路线路线简述

  • 合成目标产物 Fludrocortisone Acetate 主要起始原料 9,11-Epoxypregn-4-Ene-17,21-Diol-3,20-Dione 21-Acetate
  • (文献来源)合成步骤主要原料 9,11-Epoxypregn-4-Ene-17,21-Diol-3,20-Dione 21-Acetate
9β,11β-Epoxy-17α-Hydroxypregna-4-Ene-3,20-Dione-21-Acetate置于氟化氢吡啶体系中,用 二氯甲烷 作为反应溶剂,化学反应 2.0H,以57.4%的收率获得产物醋酸氟氢可的松
参考文献:一种氟氢可的松醋酸酯的制备方法
标题:一种氟氢可的松醋酸酯的制备方法
摘要:本发明涉及一种氟氢可的松醋酸酯的制备方法,包括:9β,11β‑环氧‑17α‑羟基孕甾‑4‑烯‑3,20‑二酮‑21‑醋酸酯与氟化试剂进行开环反应,其中所述氟化试剂为氟化氢的有机胺盐或溶液.本发明重点改良了关键工艺步骤环氧化合物开环氟化的试剂及条件,以氟化氢的有机胺盐代替高毒性,高腐蚀性的氟化氢气体,操作安全方便,氟化试剂用量少,适合工业生产.

海关参考信息

专利信息


专利号:US-8546532-B2
优先权日:2008-04-17
标题:Synthesis of directed sequence polymer compositions and antibodies thereof for the treatment of protein conformational disorders
发明人:BONNIN DUSTAN; ZANELLI ERIC; MATHERS THOMAS
权利人:BONNIN DUSTAN; ZANELLI ERIC; MATHERS THOMAS; DECLION PHARMACEUTICALS INC
摘要:The instant invention comprises a process for the solid phase synthesis of directed epitope peptide mixtures useful in the treatment and diagnosis of protein conformational disorders, such process defined by a set of rules regarding the identity and the frequency of occurrence of amino acids that substitute a base or native amino acid of a known epitope. The resulting composition is a mixture of related peptides for therapeutic use. The invention also pertains to the process of generating antibodies using the directed epitope peptide mixtures as the antigens, and antibodies generated by such process, useful in the treatment and diagnostics of the said protein conformational disorder.

专利号:US-9051302-B2
优先权日:2008-01-15
标 题 :Synthesis of resorcylic acid lactones useful as therapeutic agents
发明人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN
权利人:WINSSINGER NICOLAS; BARLUENGA SOFIA; KARPLUS MARTIN; UNIV STRASBOURG
摘要:Disclosed are macrocyclic compounds of formulae I, I′, II, II′, III, III′, IV, and V, which are analogs of the pochonin resorcylic acid lactones, pharmaceutical compositions comprising the compounds, and methods and uses comprising the compounds for the treatment of diseases mediated by kinases and Heat Shock Protein 90 HSP90.

专利号:US-8926955-B2
优先权日:2008-12-22
标题 :Synthesis of polymer conjugates of indolocarbazole compounds
发明人:BAGNOD RAFFAELLA; BECCARIA LUCA; BERTARIONE RAVA ROSSA LUISA; CRISCUOLO DOMENICO; LORENZETTO CHIARA; MAINERO VALENTINA; MARCONI ALESSANDRA; PINCELLI CARLO; TRAVERSA SILVIO
权利人:BAGNOD RAFFAELLA; BECCARIA LUCA; BERTARIONE RAVA ROSSA LUISA; CRISCUOLO DOMENICO; LORENZETTO CHIARA; MAINERO VALENTINA; MARCONI ALESSANDRA; PINCELLI CARLO; TRAVERSA SILVIO; CREABILIS S A
摘要:The present invention relates to a process for the preparation of polymer conjugates of indolocarbaxole compounds, in particular of polymer conjugates of K-252a and derivatives thereof, by a synthetic route which results in a highly pure product, with a high product yield. In a further aspect the present invention relates to novel polymer conjugates of K-252a and derivatives thereof, wherein the chemical group linking the polymer unity to the K-252a or to the K-252a derivative compound is characterized by a 5-member oxazolidindionic cyclic structure. These novel polymer conjugates are obtained through the novel synthetic route with high purity and high yields.

专利号:WO-9925385-A1
优先权日:1997-11-17
标 题:A method of increasing nucleic acid synthesis with ultrasound
发明人:UNGER EVAN C; MCCREERY THOMAS; SADEWASSER DAVID
权利人:IMARX PHARMACEUTICAL CORP
摘要:The present invention is directed to a method of increasing nucleic acid synthesis in a cell comprising administering to the cell a therapeutically effective amount of ultrasound for a therapeutically effective time such that said administration of said ultrasound results in said increased nucleic acid synthesis. The nucleic acid sequence may comprise an endogenous sequence or an exogenous sequence.

专利号:WO-2024232849-A1
优先权日:2023-05-10
标 题:A pharmaceutical composition for increasing melanin synthesis in hair follicles
发明人:BALKAN GURSES NAZ DICLE; TULUNAY MAHIR
权利人:IFL PHARMA ILAC SANAYI VE TICARET ANONIM SIRKETI
摘要:The present invention relates to a pharmaceutical composition that is developed to convert white body hair, particularly hair, back to its original color. Particularly, the invention relates to a composition that works based on the increasing mechanism of melanin synthesis by regulating melanocyte cells. The pharmaceutical composition of the present invention is applied to the scalp via an intradermal method.

专利号:US-2021244638-A1
优先权日:2018-06-05
标 题:Inhibitors of glycosphingolipid synthesis and methods of use
发明人:CHATTERJEE SUBROTO B
权利人:SUBROTO B CHATTERJEE
摘要:Compositions in the prevention and treatment of skin diseases or associated disorders, inflammation or inflammatory diseases or disorders, include at least one inhibitor of glycosphingolipid synthesis.
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主要参考文献


1: Zhao Y, Zhang K, Fent K. Corticosteroid Fludrocortisone Acetate Targets Multiple End Points in Zebrafish (Danio rerio) at Low Concentrations. Environ Sci Technol. 2016 Sep 20;50(18):10245-54. doi: 10.1021/acs.est.6b03436. Epub 2016 Sep 12. doi: 10.1097/MPG.0000000000000305. doi: 10.1111/ceo.12326. Epub 2014 May 5. doi: 10.1016/j.ijpharm.2013.03.042. Epub 2013 Mar 28. doi: 10.2332/allergolint.10-LE-0301. Epub 2011 Jun 25. doi: 10.1111/j.1939-1676.2008.0166.x. Epub 2008 Sep 4. Epub 2007 Jul 5. Review. Japanese. Japanese. Japanese.

合成参考文献


摘要:Iyakuhin Kenkyu. Study of Medical Supplies., 18(666), 1987
参考文献:10.1210/en.143.5.1889|10.1210/endo.143.5.8778
摘要:Krishnan AV, Zhao XY, Swami S, Brive L, Peehl DM, Ely KR, Feldman D. A glucocorticoid-responsive mutant androgen receptor exhibits unique ligand specificity: therapeutic implications for androgen-independent prostate cancer. Endocrinology. 2002 May;143(5):1889–900. doi: 10.1210/endo.143.5.8778.
摘要:Fujieda K. [Congenital adrenal hyperplasia]. Nihon Rinsho. 2006 May 28;Suppl 1():673–6.
摘要:Fujieda K. [Lipoid adrenal hyperplasia]. Nihon Rinsho. 2006 May 28;Suppl 1():692–5.
摘要:Fujieda K. [20,22 Desmolase deficiency]. Nihon Rinsho. 2006 May 28;Suppl 1():696–8.
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