N-(4-(4-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-p-toluenesulfonamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(4-(4-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-p-toluenesulfonamide
• 英文别名: N-[7-(4-chlorophenyl)-4-ethyl-13-methyl-3-thia-1,8,11,12-tetrazatricyclo[8.3.0.02,6]trideca-2(6),4,7,10,12-pentaen-9-yl]-4-methylbenzenesulfonamide
• 化学式: C₂₄H₂₂ClN₅O₂S₂
• 分子量: 512.056
• InChiKey: WSOWPLDCLQATLR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  34
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  126
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  6-Amino-4-(4-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine 、 异丙醚 、 对甲苯磺酰氯 在 三乙胺 作用下， 以 氯仿 为溶剂， 生成 N-(4-(4-chlorophenyl)-2-ethyl-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-p-toluenesulfonamide
  参考文献：
  名称：

  Therapeutic agent for osteoporosis and diazepine compound

  摘要：

  一种治疗骨质疏松症的药物，包含式##STR1##所示的氮杂环庚烷化合物，其中每个符号的定义如说明书中所述，或其药学上可接受的盐作为活性成分，治疗骨质疏松症的方法包括给予所述化合物，以及所述化合物用于制备治疗骨质疏松症药物的用途。式(I)的化合物具有优异的骨吸收抑制活性，并能减少由骨吸收引起的血清钙增加量。因此，这些化合物可用作药物，有效抑制骨吸收，预防骨量减少，并预防或抑制由骨吸收进展引起的血清钙含量增加，涉及佩吉特病、高钙血症、骨质疏松症等，其中骨吸收的进展被认为与症状密切相关，以及随着炎症性关节疾病如类风湿性关节炎进展，骨吸收进展（发展为骨质疏松症）的症状。

  公开号：

  US05593988A1

文献信息

• THIENODIAZEPINE COMPOUND AND MEDICINAL USE THEREOF
  申请人：YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD.

  公开号：EP0661284A1

  公开（公告）日：1995-07-05

  A thienodiazepine compound represented by general formula (I), a salt thereof, and a medicinal use thereof, wherein R³ represents a group represented by any of the following formulae: (1), -(CH₂)aN(R⁴)COR⁷ (2), -(CH₂)aN(R⁸)SO₂R⁹ (3), -(CH₂)aN(R⁸)COOR¹⁰ (4), -(CH₂)aOCON(R¹¹)(R¹²) (5), -(CH₂)aCON(R¹³(R¹⁴) (6), -(CH₂)aOCOR¹⁵ (7), -(CH₂)aOSO₂R¹⁶ (8), -(CH₂)aCOR¹⁷ (9) and -(CH₂aS(O)nR¹⁸ (10), a represents an integer of 0, 1 to 6 ; Z represents oxygen or sulfur ; and X represents oxygen or sulfur, provided that X and Y may be combined together to represent = N-N = C(R²⁰)- or = N-CH = C(R²⁰)-. This compound has CCK antagonism, gastrin antagonism and cell fusion inhibitor activity, thus being useful as a medicine.

  一种由通式（I）表示的噻唑二氮化合物，其盐以及药用途，其中R³代表以下任一式子表示的基团：（1）、-(CH₂)aN(R⁴)COR⁷（2）、-(CH₂)aN(R⁸)SO₂R⁹（3）、-(CH₂)aN(R⁸)COOR¹⁰（4）、-(CH₂)aOCON(R¹¹)(R¹²)（5）、-(CH₂)aCON(R¹³(R¹⁴)（6）、-(CH₂)aOCOR¹⁵（7）、-(CH₂)aOSO₂R¹⁶（8）、-(CH₂)aCOR¹⁷（9）和-(CH₂aS(O)nR¹⁸（10），a代表0、1至6的整数；Z代表氧或硫；X代表氧或硫，条件是X和Y可以结合在一起表示= N-N = C(R²⁰)-或= N-CH = C(R²⁰)-。该化合物具有CCK拮抗作用、胃泌素拮抗作用和细胞融合抑制剂活性，因此可用作药物。
• REMEDY FOR OSTEOPOROSIS AND DIAZEPINE COMPOUND
  申请人：YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD.

  公开号：EP0638560A1

  公开（公告）日：1995-02-15

  A remedy for osteoporosis containing a diazepine compound represented by general formula (I) or a pharmaceutically acceptable salt thereof as the active ingredient; a method of treating osteoporosis by administering the above compound; and the use of the compound for preparing a remedy for osteoporosis in formula (I) Ar represents aryl or heteroaryl; X represents oxygen or sulfur; W represents -N(R³⁶)-, -O- or -S-; Q represents a ring selected among (a), (b), (c) and (d), X and Y may be combined together to form =N-N=C(R⁶)-, =N-C(R⁵)=C(R⁶)-, =C(R⁵)-N=C(R⁶)-, =N-O-CO- or =N-N(R⁵)-CO-.

  一种治疗骨质疏松症的药物，含有通式(I)代表的二氮杂卓化合物或其药学上可接受的盐作为活性成分；一种通过施用上述化合物治疗骨质疏松症的方法；以及该化合物用于制备骨质疏松症药物的用途，在式(I)中 Ar 代表芳基或杂芳基；X代表氧或硫； W代表-N(R³⁶)-、-O-或-S-；Q 代表选自(a)、(b)、(c)和(d)的环，X 和 Y 可结合在一起形成 =N-N=C(R⁶)-、=N-C(R⁵)=C(R⁶)-、=C(R⁵)-N=C(R⁶)-、=N-O-CO- 或 =N-N(R⁵)-CO-。
• US5593988A
  申请人：——

  公开号：US5593988A

  公开（公告）日：1997-01-14
• Therapeutic agent for osteoporosis and diazepine compound
  申请人：Yoshitomi Pharmaceutical Industries, Ltd.

  公开号：US05593988A1

  公开（公告）日：1997-01-14

  A therapeutic agent for osteoporosis, comprising an azepine compound of the formula ##STR1## wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof as an active ingredient, a method for treating osteoporosis comprising administering said compound and a use of said compound for the production of a therapeutic agent for osteoporosis. The compounds of the formula (I) have superior bone resorption-inhibitory activity and act to reduce the increased amount of calcium in blood serum, which is caused by bone resorption. Accordingly, these compounds are usable as pharmaceutical agents to effectively inhibit bone resorption, to prevent decrease of bone mass and to prevent or suppress the increase of calcium amount in blood serum which is caused by the progress of bone resorption, with regard to Paget's disease, hypercalcemia, osteoporosis and so on in which the progress of bone resorption is considered to be deeply associated with the symptom, and to the symptoms of progressing bone resorption (development into osteoporosis) along with inflammatory joint diseases such as rheumatoid arthritis.

  一种治疗骨质疏松症的药物，包含式##STR1##所示的氮杂环庚烷化合物，其中每个符号的定义如说明书中所述，或其药学上可接受的盐作为活性成分，治疗骨质疏松症的方法包括给予所述化合物，以及所述化合物用于制备治疗骨质疏松症药物的用途。式(I)的化合物具有优异的骨吸收抑制活性，并能减少由骨吸收引起的血清钙增加量。因此，这些化合物可用作药物，有效抑制骨吸收，预防骨量减少，并预防或抑制由骨吸收进展引起的血清钙含量增加，涉及佩吉特病、高钙血症、骨质疏松症等，其中骨吸收的进展被认为与症状密切相关，以及随着炎症性关节疾病如类风湿性关节炎进展，骨吸收进展（发展为骨质疏松症）的症状。