CAS: 4968-09-6; Algestone Acetonide

该化合物是一种合成类固醇,是丙酮的衍生物,其特点是其结构改变,增强了其稳定性和生物活性.该化合物一般是白色到白晶状粉,可溶于乙醇和氯仿等有机溶剂,但在水中溶解性有限.ASUCTU Acetonide具有先天性,使其在生殖健康和激素治疗领域具有相关性.它经常用于避孕和荷尔蒙替代疗法的配方.该化合物的行动机制涉及对丙酯受体的约束性,导致各种生理影响,包括调节月经循环和保持妊娠.由于其腐蚀性质,它也可能产生某些诱发性或诱导性影响,尽管这些影响一般不那么明显.安全性和有效性简介对于其治疗应用至关重要,并且受制药方面的监管.

结构式图片

MSDS等安全信息

    上下游产品

    CAS号27336-10-3 3β-acetoxy-16α,... | CAS号26302-61-4 3β,-hydroxy-16α...

    合成工艺路线路线简述

      📜3β-Acetoxy-16α,17α-Isopropylidenedioxypregn-5-Ene-20-One置于disodium Hydrogenphosphate,Potassium Dihydrogenphosphate,葡萄糖,Corn-Steep Liquor体系中,用 水,N,N-二甲基甲酰胺 作为反应溶剂,化学反应 15.0H,以75%的收率获得产物阿孕奈德
      参考文献:Synthesis Of 9α-Hydroxysteroids By A Rhodococcus Sp.
      标题:Synthesis Of 9α-Hydroxysteroids By A Rhodococcus Sp.
      摘要:9 Alpha-Hydroxylation Of Delta 5-3 Beta-Hydroxysteroids (Of Androstane,Pregnane,24-Nor-And 21,24-Bisnorcholane Groups) Was Carried Out By A Rhodococcus Sp.,Isolated From A Petroleum-Containing Soil Sample. A Large Number Of The Investigated Steroids Was Transformed Into 9 Alpha-Hydroxy-Delta 4-3-Ketones In Satisfactory Yields (50-90%) At High Initial Concentrations Of The Substrates (0.5-5.0 G/l). The Influence Of Some Structural Features Of The Steroid Molecule On The Progress And Effectiveness Of The Microbial Transformation Was Also Shown.
      DOI:10.1016/0039-128X(89)90002-0

      海关参考信息

      专利信息


      专利号:US-2013035307-A1
      优先权日:2010-01-26
      标 题:Methods for treating or preventing the spread of cancer using semi-synthetic glycosaminoglycosan ethers
      发明人:PRESTWICH GLENN D; KENNEDY THOMAS P
      权利人:UNIV UTAH RES FOUND; PRESTWICH GLENN D; KENNEDY THOMAS P
      摘要:Described herein are methods for the treatment and prevention of tumor metastasis using alkylated and fluoroalkylated semi-synthetic glycosaminoglycan ethers (“SAGEsâ€?). The synthesis of sulfated alkylated and fluoroalkylated SAGEs is also described.

      专利号:WO-2023096715-A9
      优先权日:2021-10-22
      标 题:Immunomodulatory glycosphingolipids and methods of use thereof
      发明人:KASPER DENNIS; OH SUNGWHAN
      权利人:HARVARD COLLEGE
      摘要:Provided herein are a subset of alpha-galactosylceramide (alpha-GC) compounds having improved immunomodulatory activity, particularly with respect to NKT cell number and activity. Also provided herein are methods of use of such compounds, including in the modulation of NKT cells and/or activity in vivo. Further provided are combinatorial synthesis methods for generating alpha-GC compounds of specifically defined structure and thereby generating pure preparations thereof.

      专利号:US-2022125838-A1
      优先权日:2019-02-11
      标题 :Immunomodulatory glycosphingolipids and methods of use thereof
      发明人:OH SUNGWHAN; KASPER DENNIS L; SONG HEEBUM; PARK SEUNG BUM
      权利人:HARVARD COLLEGE; SEOUL NAT UNIV R&DB FOUNDATION
      摘要:Provided herein are a subset of alpha-galactosylceramide (alpha-GC) compounds having improved immunomodulatory activity, particularly with respect to NKT cell number and activity. Also provided herein are methods of use of such compounds, including in the modulation of NKT cells and/or activity in vivo. Further provided are combinatorial synthesis methods for generating alpha-GC compounds of specifically defined structure and thereby generating pure preparations thereof.

      专利号:US-9907753-B2
      优先权日:2010-03-19
      标 题 :Lipid vesicle compositions and methods of use
      发明人:IRVINE DARRELL J; MOON JAEHYUN
      权利人:MASSACHUSETTS INST TECHNOLOGY
      摘要:The invention provides delivery systems comprised of stabilized multilamellar vesicles, as well as compositions, methods of synthesis, and methods of use thereof. The stabilized multilamellar vesicles may comprise prophylactic, therapeutic and/or diagnostic agents.

      专利号:EP-4058432-A1
      优先权日:2019-11-14
      标 题:Improved synthesis of kras g12c inhibitor compound

      专利号:US-3316157-A
      优先权日:1963-12-18
      标题:Synthesis of steroids
      发明人:ANDREW DIASSI PATRICK; ANTHONY PRINCIPE PACIFICO
      权利人:SQUIBB & SONS INC

      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: Gent R, du Toit T, Swart AC. 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro. J Steroid Biochem Mol Biol. 2019 Jul;191:105369. doi: 10.1016/j.jsbmb.2019.04.018. Epub 2019 Apr 27. doi: 10.3389/fendo.2015.00037. eCollection 2015.
      3: Gallo MF, Grimes DA, Lopez LM, Schulz KF, d'Arcangues C. Combination injectable contraceptives for contraception. Cochrane Database Syst Rev. 2013;3:CD004568. Review.

      合成参考文献


      摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
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