1(2)H-indazole-6-sulfonic acid | 858227-63-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡唑类
• 英文名称: 1(2)H-indazole-6-sulfonic acid
• 英文别名: 1(2)H-Indazol-6-sulfonsaeure；1H-Indazole-6-sulfonic acid
• CAS: 858227-63-1
• 化学式: C₇H₆N₂O₃S
• 分子量: 198.202
• InChiKey: XACLCVLPIZBCPA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  91.4
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 乙醇 、 锌 作用下， 生成 1(2)H-indazole-6-sulfonic acid
  参考文献：
  名称：

  Petitcolas; Sureau, Bulletin de la Societe Chimique de France, 1950, p. 466,476

  摘要：

  DOI：

文献信息

• Sulfonylaminovalerolactams and derivatives thereof as factor Xa inhibitors
  申请人：Han Wei

  公开号：US20050096309A1

  公开（公告）日：2005-05-05

  The present application describes sulfonylaminovalerolactams and derivatives thereof of Formula Ia-If: or pharmaceutically acceptable salt forms thereof, wherein ring G is a mono- or bicyclic carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.

  本申请描述了Formula Ia-If的磺酰氨基戊内内酰胺及其衍生物，或其药用可接受的盐形式，其中环G为单环或双环碳环或杂环。本发明的化合物可用作胰蛋白酶样丝氨酸蛋白酶抑制剂，特别是因子Xa的抑制剂。
• INDAZOLE SULFONAMIDE DERIVATIVES AS INVERSE AGONISTS OF RETINOID-RELATED ORPHAN RECEPTOR GAMMA (ROR GAMMA (T))
  申请人：GALDERMA RESEARCH & DEVELOPMENT

  公开号：US20170342062A1

  公开（公告）日：2017-11-30

  Indazole sulfonamide derivatives of formula (I), the pharmaceutically acceptable addition salts thereof, the hydrates and/or solvates thereof, and the use of same as inverse agonists of retinoid-related orphan receptor gamma RORγt are described. Pharmaceutical compositions including such compounds, as well as the use thereof for the topical and/or oral treatment of RORγt receptor-mediated inflammatory diseases, in particular acne, psoriasis and/or atopic dermatitis are also described.

  本发明涉及式(I)的吲唑磺胺衍生物，其药学上可接受的加盐物，其水合物和/或溶剂合物，以及将其用作视黄醇相关孤儿受体伽玛RORγt的逆向激动剂的用途。还描述了包括这些化合物的药物组合物，以及将其用于治疗RORγt受体介导的炎症性疾病，特别是痤疮、银屑病和/或特应性皮炎的局部和/或口服治疗。
• SULFONYLAMINOVALEROLACTAMS AND DERIVATIVES THEREOF AS FACTOR XA INHIBITORS
  申请人：Han Wei

  公开号：US20070099922A1

  公开（公告）日：2007-05-03

  The present application describes sulfonylaminovalerolactams and derivatives thereof of Formula Ia-If: or pharmaceutically acceptable salt forms thereof, wherein ring G is a mono- or bicyclic carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.

  本申请描述了式Ia-If的磺酰氨基戊内酰内酰胺及其衍生物或其药学上可接受的盐形式，其中环G是单环或双环碳环或杂环。本发明的化合物可用作胰蛋白酶样丝氨酸蛋白酶的抑制剂，特别是Xa因子的抑制剂。
• Indazole sulfonamide derivatives as inverse agonists of retinoid-related orphan receptor gamma (ROR γ (T))
  申请人：GALDERMA RESEARCH & DEVELOPMENT

  公开号：US10246440B2

  公开（公告）日：2019-04-02

  Indazole sulfonamide derivatives of formula (I), the pharmaceutically acceptable addition salts thereof, the hydrates and/or solvates thereof, and the use of same as inverse agonists of retinoid-related orphan receptor gamma RORγt are described. Pharmaceutical compositions including such compounds, as well as the use thereof for the topical and/or oral treatment of RORγt receptor-mediated inflammatory diseases, in particular acne, psoriasis and/or atopic dermatitis are also described.

  本发明描述了式(I)的吲唑磺酰胺衍生物、其药学上可接受的加成盐、其水合物和/或溶剂，以及其作为维甲酸相关孤儿受体γ RORγt的逆激动剂的用途。 此外，还介绍了包括此类化合物的药物组合物，以及将其用于局部和/或口服治疗 RORγt 受体介导的炎症性疾病，特别是痤疮、牛皮癣和/或特应性皮炎的方法。
• Indazole sulfonamide derivatives as inverse agonists of retinoid-related orphan receptor gamma (ROR gamma (T))
  申请人：GALDERMA RESEARCH & DEVELOPMENT

  公开号：US10752617B2

  公开（公告）日：2020-08-25

  Indazole sulfonamide derivatives of formula (I), the pharmaceutically acceptable addition salts thereof, the hydrates and/or solvates thereof, and the use of same as inverse agonists of retinoid-related orphan receptor gamma RORγt are described. Pharmaceutical compositions including such compounds, as well as the use thereof for the topical and/or oral treatment of RORγt receptor-mediated inflammatory diseases, in particular acne, psoriasis and/or atopic dermatitis are also described.

  本发明描述了式(I)的吲唑磺酰胺衍生物、其药学上可接受的加成盐、其水合物和/或溶剂，以及其作为维甲酸相关孤儿受体γ RORγt的逆激动剂的用途。此外，还介绍了包括此类化合物的药物组合物，以及将其用于局部和/或口服治疗 RORγt 受体介导的炎症性疾病，特别是痤疮、牛皮癣和/或特应性皮炎的方法。