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2-(4-oxo-3-((5-(trifluoromethyl)benzo[d]thiazol-2-yl)methyl)-3,4-dihydrothieno[3,4-d]pyridazin-1-yl)acetic acid | 2170729-29-8

中文名称
——
中文别名
——
英文名称
2-(4-oxo-3-((5-(trifluoromethyl)benzo[d]thiazol-2-yl)methyl)-3,4-dihydrothieno[3,4-d]pyridazin-1-yl)acetic acid
英文别名
2-(4-Oxo-3-((5-(trifluoromethyl)benzo[d]thiazol-2-yl)methyl)-3,4-dihydrothieno[3,4-d]pyridazin-1-yl)acetic acid;2-[4-oxo-3-[[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl]thieno[3,4-d]pyridazin-1-yl]acetic acid
2-(4-oxo-3-((5-(trifluoromethyl)benzo[d]thiazol-2-yl)methyl)-3,4-dihydrothieno[3,4-d]pyridazin-1-yl)acetic acid化学式
CAS
2170729-29-8
化学式
C17H10F3N3O3S2
mdl
——
分子量
425.412
InChiKey
ORQGHAJIWGGFJK-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

物化性质

  • 沸点:
    610.3±65.0 °C(Predicted)
  • 密度:
    1.72±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    139
  • 氢给体数:
    1
  • 氢受体数:
    10

安全信息

  • 危险性防范说明:
    P261,P280,P301+P312,P302+P352,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    -20°C,密闭保存,干燥环境

制备方法与用途

AT-007是一种口服活性的中枢神经系统渗透性醛糖还原酶抑制剂,用于治疗半乳糖血症,其IC50值为100皮摩尔。

反应信息

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文献信息

  • Aldose reductase inhibitors and methods of use thereof
    申请人:THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
    公开号:US10150779B2
    公开(公告)日:2018-12-11
    The present disclosure relates to novel compounds and pharmaceutical compositions thereof, and methods for promoting healthy aging of skin, the treatment of skin disorders, the treatment of cardiovascular disorders, the treatment of renal disorders, the treatment of angiogenesis disorders, such as cancer, treatment of tissue damage, such as non-cardiac tissue damage, the treatment of evolving myocardial infarction, the treatment of ischemic injury, and the treatment of various other disorders, such as complications arising from diabetes with the compounds and compositions of the invention. Other disorders can include, but are not limited to, atherosclerosis, coronary artery disease, diabetic nephropathy, diabetic neuropathy, diabetic retinopathy, diabetic cardiomyopathy, infections of the skin, peripheral vascular disease, stroke, asthma, and the like.
    本公开涉及新型化合物及其药物组合物,以及促进皮肤健康老化、治疗皮肤疾病、治疗心血管疾病、治疗肾脏疾病、治疗血管生成疾病(如癌症)、治疗组织损伤(如非心脏组织损伤)、治疗演变性心肌梗塞、治疗缺血性损伤,以及用本发明化合物和组合物治疗各种其他疾病(如糖尿病引起的并发症)的方法。其他疾病包括但不限于动脉粥样硬化、冠状动脉疾病、糖尿病肾病、糖尿病神经病变、糖尿病视网膜病变、糖尿病心肌病、皮肤感染、外周血管疾病、中风、哮喘等。
  • ALDOSE REDUCTASE INHIBITORS AND METHODS OF USE THEREOF
    申请人:The Trustees of Columbia University in the City of New York
    公开号:EP3352754A1
    公开(公告)日:2018-08-01
  • EP3757107A1
    申请人:——
    公开号:EP3757107A1
    公开(公告)日:2020-12-30
  • COMPOSITIONS AND METHODS FOR TREATING GALACTOSEMIA
    申请人:Applied Therapeutics, Inc.
    公开号:US20200230139A1
    公开(公告)日:2020-07-23
    The disclosure relates to methods for treating galactosemia and manifestations of galactosemia using aldose reductase inhibitors.
  • INHIBITORS OF ALDOSE REDUCTASE
    申请人:Applied Therapeutics, Inc.
    公开号:US20220017535A1
    公开(公告)日:2022-01-20
    The present disclosure relates to novel compounds and pharmaceutical compositions thereof, and methods for promoting healthy aging of skin, the treatment of skin disorders, the treatment of cardiovascular disorders, the treatment of renal disorders, the treatment of angiogenesis disorders, such as cancer, treatment of tissue damage, such as non-cardiac tissue damage, the treatment of evolving myocardial infarction, the treatment of ischemic injury, and the treatment of various other disorders, such as complications arising from diabetes with the compounds and compositions of the invention. Other disorders can include, but are not limited to, atherosclerosis, cardiomyopathy, coronary artery disease, diabetic nephropathy, diabetic neuropathy, diabetic retinopathy, diabetic cardiomyopathy, infections of the skin, peripheral vascular disease, stroke, galactosemia, asthma, PMM2-CDG and the like.
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