6-Chloropregna-1,4,6-triene-3,20-dione | 5192-84-7

• 物质功能分类: 有机原料 - 酮类化合物
• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 6-Chloropregna-1,4,6-triene-3,20-dione
• 英文别名: 17-acetyl-6-chloro-10,13-dimethyl-8,9,11,12,14,15,16,17-octahydrocyclopenta[a]phenanthren-3-one
• CAS: 5192-84-7
• 化学式: C₂₁H₂₅ClO₂
• 分子量: 344.9
• InChiKey: USXVMPAWZOOYDE-UHFFFAOYSA-N

物化性质

• 熔点：
  208-209° (dec)
• 沸点：
  478.6±45.0 °C(Predicted)
• 密度：
  1.20±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  24
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• Nitric Oxide Releasing Prodrugs of Therapeutic Agents
  申请人：SATYAM Apparao

  公开号：US20110263526A1

  公开（公告）日：2011-10-27

  The present invention relates to nitric oxide releasing prodrugs of known drugs or therapeutic agents which are represented herein as compounds of formula (I) wherein the drugs or therapeutic agents contain one or more functional groups independently selected from a carboxylic acid, an amino, a hydroxyl and a sulfhydryl group. The invention also relates to processes for the preparation of the nitric oxide releasing prodrugs (the compounds of formula (I)), to pharmaceutical compositions containing them and to methods of using the prodrugs.

  本发明涉及已知药物或治疗剂的一氧化氮释放前药，其在此处表示为式(I)的化合物，其中药物或治疗剂包含一个或多个功能基团，独立地选自羧酸、氨基、羟基和巯基。该发明还涉及制备一氧化氮释放前药（式(I)的化合物）的方法，含有它们的药物组合物以及使用这些前药的方法。
• Technology for the Preparation of Microparticles
  申请人：Malakhov Michael

  公开号：US20090098207A1

  公开（公告）日：2009-04-16

  Microspheres are produced by contacting a solution of a macromolecule or small molecule in a solvent with an antisolvent and a counterion, and chilling the solution. The microspheres are useful for preparing pharmaceuticals, nutraceuticals, cosmetic products and the like of defined dimensions.

  微球是通过将溶液中的大分子或小分子与抗溶剂和对离子接触，并冷却溶液而制备的。这些微球可用于制备具有明确定义尺寸的药物、营养保健品、化妆品等产品。
• PROCESS FOR THE PREPARATION OF 17BETA-HYDROXY-DES-A-ANDROST-9,10-EN-5-ONE
  申请人：INDUSTRIALE CHIMICA S.R.L.

  公开号：US20180339956A1

  公开（公告）日：2018-11-29

  The present invention relates to a new process for the synthesis of 17β-hydroxy-des-A-androst-9,10-en-5-one, the compound of the following formula (1), which can be used as an intermediate in the synthesis of retroprogesterones.

  本发明涉及一种合成17β-羟基-去氢-A-雄烯-9,10-烯-5-酮的新工艺，该化合物的化学式为(1)，可用作合成反孕激素的中间体。
• [EN] PROCESS FOR THE PREPARATION OF 17BETA-HYDROXY-DES-A-ANDROST-9,10-EN-5-ONE<br/>[FR] PROCÉDÉ DE PRÉPARATION DE 17 BÊTA-HYDROXY-DES-A-ANDROST-9,10-EN-5-ONE
  申请人：IND CHIMICA SRL

  公开号：WO2017072719A1

  公开（公告）日：2017-05-04

  The present invention relates to a new process for the synthesis of 17β-hydroxy- des-A-androst-9,10-en-5-one, the compound of the following formula (1), which can be used as an intermediate in the synthesis of retroprogesterones.

  本发明涉及一种新的合成17β-羟基-去氢A-雄烯-9,10-烯-5-酮的方法，该化合物的化学式为（1），可以用作合成反孕激素的中间体。
• Compositions and methods to effect the release profile in the transdermal administration of active agents
  申请人：——

  公开号：US20020004065A1

  公开（公告）日：2002-01-10

  Compositions and methods for the transdermal delivery of active agents up to a period of seven days or more at substantially a zero-order release rate comprising a pharmaceutically acceptable adhesive matrix and a polymeric plastic material that provides a release rate regulating effect on the active agents.

  本发明涉及一种用于经皮递送活性药剂的组合物和方法，该组合物和方法能够在持续时间为七天或更长时间内以几乎零阶释放速率递送活性药剂，包括一种药学上可接受的粘合基质和一种聚合物塑料材料，该聚合物塑料材料对活性药剂具有释放速率调节作用。