N-{4-[3-(4-benzyl-piperidin-1-yl)-propyl]-phenyl}-N-(4-hydroxy-benzyl)-benzenesulfonamide | 675868-00-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: N-{4-[3-(4-benzyl-piperidin-1-yl)-propyl]-phenyl}-N-(4-hydroxy-benzyl)-benzenesulfonamide
• 英文别名: N-[4-[3-(4-benzylpiperidin-1-yl)propyl]phenyl]-N-[(4-hydroxyphenyl)methyl]benzenesulfonamide
• CAS: 675868-00-5
• 化学式: C₃₄H₃₈N₂O₃S
• 分子量: 554.753
• InChiKey: ZUPFPKAXBHPXQD-UHFFFAOYSA-N

物化性质

• 沸点：
  721.4±70.0 °C(Predicted)
• 密度：
  1.212±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  40
• 可旋转键数：
  11
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  69.2
• 氢给体数：
  1
• 氢受体数：
  5

文献信息

• [EN] AMIDE AND SULFONAMIDE LIGANDS FOR THE ESTROGEN RECEPTOR<br/>[FR] LIGANDS D'AMIDES ET DE SULFONAMIDES DU RECEPTEUR OESTROGENIQUE
  申请人：PFIZER PROD INC

  公开号：WO2004026823A1

  公开（公告）日：2004-04-01

  The present invention provides estrogen receptor (ER) ligands of structural formula (I) the pharmaceutically acceptable salts, stereoisomers, and prodrugs thereof, and the pharmaceutically acceptable salts of the prodrugs, wherein R1, R2, R3, R4, R5, X, and Q are as defined herein. The invention further provides pharmaceutical compositions comprising the compounds of formula (I), and methods for treating or preventing diseases, disorders, conditions, or symptoms mediated by an ER which comprise administering to a mammalian subject in need of treatment therewith, an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, or a pharmaceutically acceptable salt of the prodrug, or a pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, or a pharmaceutically acceptable salt of the prodrug. The invention further provides pharmaceutical compositions comprising combinations of the compounds of formula (I) and one or more of sodium fluoride, estrogen, a bone anabolic agent, a growth hormone or growth hormone secretagogue, a prostaglandin agonist/antagonist, and a parathyroid hormone, and methods of treating or preventing diseases, disorders, conditions, or symptoms mediated by an ER comprising the administration of an effective amount of such combination to a mammalian subject in need of treatment therewith.

  本发明提供了结构式（I）的雌激素受体（ER）配体及其药用盐、立体异构体和前药，以及前药的药用盐，其中R1、R2、R3、R4、R5、X和Q如本文所定义。该发明还提供了包括式（I）化合物的药物组合物，以及用于治疗或预防由ER介导的疾病、紊乱、症状或症状的方法，包括向需要治疗的哺乳动物主体施用式（I）化合物的有效量，或其药用盐、立体异构体或前药，或前药的药用盐，或包括式（I）化合物的药物组合物，或其药用盐、立体异构体或前药，或前药的药用盐。该发明还提供了包括式（I）化合物和一种或多种氟化钠、雌激素、骨骼阳性代理、生长激素或生长激素分泌素、前列腺素激动剂/拮抗剂和甲状旁腺激素的药物组合物的药物组合物，以及治疗或预防由ER介导的疾病、紊乱、症状或症状的方法，包括向需要治疗的哺乳动物主体施用这种组合物的有效量。
• Acyclic amide and sulfonamide ligands for the estrogen receptor
  申请人：Pfizer Inc

  公开号：US20040110767A1

  公开（公告）日：2004-06-10

  The present invention provides estrogen receptor (ER) ligands of structural formula (I) 1 the pharmaceutically acceptable salts, stereoisomers, and prodrugs thereof, and the pharmaceutically acceptable salts of the prodrugs, wherein R 1 , R 2 , R 3 , R 4 , R 5 , X, and Q are as defined herein. The invention further provides pharmaceutical compositions comprising the compounds of formula (I), and methods for treating or preventing diseases, disorders, conditions, or symptoms mediated by an ER which comprise administering to a mammalian subject in need of treatment therewith, an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, or a pharmaceutically acceptable salt of the prodrug, or a pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, or a pharmaceutically acceptable salt of the prodrug. The invention further provides pharmaceutical compositions comprising combinations of the compounds of formula (I) and one or more of sodium fluoride, estrogen, a bone anabolic agent, a growth hormone or growth hormone secretagogue, a prostaglandin agonist/antagonist, and a parathyroid hormone, and methods of treating or preventing diseases, disorders, conditions, or symptoms mediated by an ER comprising the administration of an effective amount of such combination to a mammalian subject in need of treatment therewith.

  本发明提供了结构式(I)的雌激素受体（ER）配体，其包括其药学上可接受的盐、立体异构体和前药，以及前药的药学上可接受的盐，其中R1、R2、R3、R4、R5、X和Q如本文所定义。本发明还提供了包括式(I)化合物的制药组合物以及治疗或预防由ER介导的疾病、失调、症状或症状的方法，该方法包括向需要治疗的哺乳动物主体中给予式(I)化合物的有效量，或其药学上可接受的盐、立体异构体或前药，或前药的药学上可接受的盐，或包括式(I)化合物的制药组合物，或其药学上可接受的盐、立体异构体或前药，或前药的药学上可接受的盐。本发明还提供了包括式(I)化合物和一种或多种氟化钠、雌激素、骨质增生剂、生长激素或生长激素分泌素、前列腺素激动剂/拮抗剂和甲状旁腺激素的制药组合物，以及通过向需要治疗的哺乳动物主体中给予该组合物的有效量来治疗或预防由ER介导的疾病、失调、症状或症状的方法。
• AMIDE AND SULFONAMIDE LIGANDS FOR THE ESTROGEN RECEPTOR
  申请人：Pfizer Products Inc.

  公开号：EP1542967A1

  公开（公告）日：2005-06-22
• US7053212B2
  申请人：——

  公开号：US7053212B2

  公开（公告）日：2006-05-30