7-hydroxy-3-(4-hydroxyphenyl)-3-methylchroman-4-one | 344397-70-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 7-hydroxy-3-(4-hydroxyphenyl)-3-methylchroman-4-one
• 英文别名: (+)-7-Hydroxy-3-(4-hydroxyphenyl)-3-methylchroman-4-one；7-hydroxy-3-(4-hydroxyphenyl)-3-methyl-2H-chromen-4-one
• CAS: 344397-70-2
• 化学式: C₁₆H₁₄O₄
• 分子量: 270.285
• InChiKey: BYBOFORQEWLDRN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  66.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  7-hydroxy-3-(4-hydroxyphenyl)-3-methylchroman-4-one 生成 (3'RS,4'RS)-11-[7-hydroxy-3-(4-hydroxyphenyl)-3-methylchroman-4-yl]-2-(4,4,5,5,5-pentafluoropentyl)undecanoic acid
  参考文献：
  名称：

  Optically active chroman and thiochroman derivatives

  摘要：

  本发明包括具有以下通式（1）的化合物：1式中，X代表氧原子或硫原子，m表示2到14的整数，n表示2到7的整数，或其水合物或药学上可接受的盐。通式（1）的化合物在制药应用中具有优越的抗雌激素活性，因为其比相应的外消旋混合物具有更好的效果。

  公开号：

  US20030125571A1

文献信息

• 3-methyl-chroman and -thiochroman derivatives
  申请人：Chugai Seiyaku Kabushiki Kaisha

  公开号：US06552069B1

  公开（公告）日：2003-04-22

  The present invention provides a compound having the following general formula (1): in which R1 represents a hydrogen atom, etc.; R2 represents a C3-C3 perhalogenoalkyl group, etc.; each of R3 and R4 independently represents a hydrogen atom, etc.; X represents an oxygen atom or a sulfur atom; m represents an integer of 2 to 14; and n represents an integer of 0 to 8; or enantiomers of the compound, or hydrates or pharmaceutically acceptable salts of the compound or its enantiomers. The compound of general formula (1) is advantageous in pharmaceutical use because of its anti-estrogenic activity.

  本发明提供了具有以下一般式（1）的化合物： 其中R1代表氢原子等；R2代表C3-C3全卤代烷基等；R3和R4各自独立地代表氢原子等；X代表氧原子或硫原子；m代表2至14的整数；n代表0至8的整数；或该化合物的对映体、水合物或药用可接受的盐。一般式（1）的化合物在药用上具有抗雌激素活性，具有优势。
• Novel benzopyran or thiobenzopyran derivatives
  申请人：Chugai Seiyaku Kabushiki Kaisha

  公开号：US20040102479A1

  公开（公告）日：2004-05-27

  The present invention relates to a novel benzopyran or thiobenzopyran derivative represented by formula (1): pharmaceutically acceptable salt or stereoisomer thereof, in which X, R 1 , R 2 , R 3 , R 4 and A are defined as described in the specification, and to a process for preparation thereof and a pharmaceutical composition having anti-estrogenic activity which contains the compound (1) as an active component.

  本发明涉及一种由式（1）表示的新型苯并吡喃或硫代苯并吡喃衍生物：其药学上可接受的盐或立体异构体，其中X，R1，R2，R3，R4和A的定义如说明书中所述，以及制备过程和具有抗雌激素活性的制剂，其含有化合物（1）作为活性成分。
• Benzopyran or thiobenzopyran derivatives
  申请人：Chugai Seiyaku Kabushiki Kaisha

  公开号：US07074819B2

  公开（公告）日：2006-07-11

  The present invention relates to a novel benzopyran or thiobenzopyran derivative represented by formula (1): pharmaceutically acceptable salt or stereoisomer thereof, in which X, R1, R2, R3, R4 and A are defined as described in the specification, and to a process for preparation thereof and a pharmaceutical composition having anti-estrogenic activity which contains the compound (1) as an active component.

  本发明涉及一种由式（1）所表示的新型苯并吡喃或硫代苯并吡喃衍生物：其药学上可接受的盐或立体异构体，其中X、R1、R2、R3、R4和A的定义如说明书所述，以及制备该化合物的方法和含有化合物（1）作为活性成分的具有抗雌激素活性的药物组合物。
• OPTICALLY ACTIVE CHROMAN AND THIOCHROMAN DERIVATIVES
  申请人：CHUGAI SEIYAKU KABUSHIKI KAISHA

  公开号：EP1241165A1

  公开（公告）日：2002-09-18

  The present invention includes a compound having the following general formula (1): in which Xrepresents an oxygen atom or a sulfur atom, mrepresents an integer of 2 to 14, and nrepresents an integer of 2 to 7, or hydrates or pharmaceutically acceptable salts thereof. The compound of general formula (1) is advantageous in pharmaceutical use because of its far superior anti-estrogenic activity over the corresponding racemic mixture.

  本发明包括具有以下通式(1)的化合物： 其中 X代表氧原子或硫原子、 m代表 2 至 14 的整数，和 n 代表 2 至 7 的整数、 或其水合物或药学上可接受的盐。通式（1）化合物的抗雌激素活性远远优于相应的外消旋混合物，因此在医药用途中具有优势。
• 3-METHYL-CHROMAN AND -THIOCHROMAN DERIVATIVES
  申请人：CHUGAI SEIYAKU KABUSHIKI KAISHA

  公开号：EP1241166A1

  公开（公告）日：2002-09-18

  The present invention provides a compound having the following general formula (1): in which    R1 represents a hydrogen atom, etc.;    R2 represents a C3-C5 perhalogenoalkyl group, etc.;    each of R3 and R4 independently represents a hydrogen atom, etc.;    X represents an oxygen atom or a sulfur atom;    m represents an integer of 2 to 14; and    n represents an integer of 0 to 8; or enantiomers of the compound, or hydrates or pharmaceutically acceptable salts of the compound or its enantiomers. The compound of general formula (1) is advantageous in pharmaceutical use because of its anti-estrogenic activity.

  本发明提供了具有以下通式(1)的化合物： 其中 R1 代表氢原子等 R2 代表 C3-C5 全卤代烷基等； R3 和 R4 各自独立地代表氢原子等； X 代表氧原子或硫原子； m 代表 2 至 14 的整数；以及 n 代表 0 至 8 的整数； 或该化合物的对映体，或该化合物或其对映体的水合物或药学上可接受的盐。通式（1）化合物具有抗雌激素活性，因此在医药用途中具有优势。