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2-(1,1,1-Trifluoro-2-methylpropan-2-yl)pyrazol-3-amine

中文名称
——
中文别名
——
英文名称
2-(1,1,1-Trifluoro-2-methylpropan-2-yl)pyrazol-3-amine
英文别名
2-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrazol-3-amine
2-(1,1,1-Trifluoro-2-methylpropan-2-yl)pyrazol-3-amine化学式
CAS
——
化学式
C7H10F3N3
mdl
——
分子量
193.17
InChiKey
XKUCVWZBHJRUIW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    43.8
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] PYRIDINE DERIVATIVES AS REARRANGED DURING TRANSFECTION (RET) KINASE INHIBITORS<br/>[FR] DÉRIVÉS PYRIDINE UTILISÉS COMME INHIBITEURS DE LA KINASE RÉARRANGÉE AU COURS DE LA TRANSFECTION (RET)
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2014141187A1
    公开(公告)日:2014-09-18
    This invention relates to novel compounds which are inhibitors of the Rearranged during Transfection (RET) kinase, to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy, alone or in combination, for the normalization of gastrointestinal sensitivity, motility and/or secretion and/or abdominal disorders or diseases and/or treatment related to diseases related to RET dysfunction or where modulation of RET activity may have therapeutic benefit including but not limited to all classifications of irritable bowel syndrome (IBS) including diarrhea-predominant, constipation-predominant or alternating stool pattern, functional bloating, functional constipation, functional diarrhea, unspecified functional bowel disorder, functional abdominal pain syndrome, chronic idiopathic constipation, functional esophageal disorders, functional gastroduodenal disorders, functional anorectal pain, inflammatory bowel disease, proliferative diseases such as non-small cell lung cancer, hepatocellular carcinoma, colorectal cancer, medullary thyroid cancer, follicular thyroid cancer, anaplastic thyroid cancer, papillary thyroid cancer, brain tumors, peritoneal cavity cancer, solid tumors, other lung cancer, head and neck cancer, gliomas, neuroblastomas, Von Hippel-Lindau Syndrome and kidney tumors, breast cancer, fallopian tube cancer, ovarian cancer, transitional cell cancer, prostate cancer, cancer of the esophagus and gastroesophageal junction, biliary cancer, adenocarcinoma, and any malignancy with increased RET kinase activity.
    这项发明涉及一种新型化合物,它们是重排基因转位(RET)激酶的抑制剂,包括含有它们的药物组合物,它们的制备方法,以及它们在治疗中的使用,单独或结合使用,用于规范胃肠敏感性、蠕动和/或分泌以及/或腹部紊乱或疾病的治疗,或与与RET功能障碍相关的疾病相关的治疗,或者调节RET活性可能具有治疗益处的治疗,包括但不限于所有分类的肠易激综合征(IBS),包括以腹泻为主、以便秘为主或交替排便模式、功能性腹胀、功能性便秘、功能性腹泻、未特指的功能性肠道障碍、功能性腹痛综合征、慢性特发性便秘、功能性食管障碍、功能性胃十二指肠障碍、功能性肛门疼痛、炎症性肠病、非小细胞肺癌、肝细胞癌、结肠癌、髓样甲状腺癌、滤泡性甲状腺癌、间变性甲状腺癌、乳头状甲状腺癌、脑肿瘤、腹腔癌、实体肿瘤、其他肺癌、头颈癌、神经胶质瘤、神经母细胞瘤、冯·希普-林道综合征和肾肿瘤、乳腺癌、输卵管癌、卵巢癌、移行细胞癌、前列腺癌、食管和胃食管交界处癌症、胆道癌、腺癌,以及任何具有增加RET激酶活性的恶性肿瘤。
  • [EN] KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASE
    申请人:RESPIVERT LTD
    公开号:WO2014076484A1
    公开(公告)日:2014-05-22
    There are provided compounds of formula I, (I) wherein R1 to R5, Ar and X1 to X3 have meanings given in the description, which compounds have antiinflammatory activity (e.g. through inhibition of one or more of members of: the family of p38 mitogen-activated protein kinase enzymes; Syk kinase; and members of the Src family of tyrosine kinases) and have use in therapy, including in pharmaceutical combinations, especially in the treatment of inflammatory diseases, including inflammatory diseases of the lung, eye and intestines.
    提供了化合物I的化合物,化合物I的化合物中R1至R5,Ar以及X1至X3具有描述中给定的含义,这些化合物具有抗炎活性(例如通过抑制p38丝裂原活化蛋白激酶酶家族中的一个或多个成员;Syk激酶;以及酪氨酸激酶Src家族的成员之一)并且在治疗中有用,包括在药物组合中,特别是用于治疗炎症性疾病,包括肺部、眼睛和肠道的炎症性疾病。
  • KINASE INHIBITORS
    申请人:Respivert Limited
    公开号:EP2925742A1
    公开(公告)日:2015-10-07
  • PYRIDINE DERIVATIVES AS REARRANGED DURING TRANSFECTION (RET) KINASE INHIBITORS
    申请人:GlaxoSmithKline Intellectual Property Development Limited
    公开号:EP2970191A1
    公开(公告)日:2016-01-20
  • 9H-PYRIMIDO[4,5-B]INDOLES AND RELATED ANALOGS AS BET BROMODOMAIN INHIBITORS
    申请人:The Regents of The University of Michigan
    公开号:EP3110818A1
    公开(公告)日:2017-01-04
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