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AS5

中文名称
——
中文别名
——
英文名称
AS5
英文别名
N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-fluorobenzenesulfonamide;N-(3-(3,5-Dimethoxyphenylamino)quinoxalin-2-yl)-4-fluorobenzenesulfonamide;N-[3-(3,5-dimethoxyanilino)quinoxalin-2-yl]-4-fluorobenzenesulfonamide
AS5化学式
CAS
——
化学式
C22H19FN4O4S
mdl
——
分子量
454.482
InChiKey
IKCRYIPVXLGUJT-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):
    4
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    111
  • 氢给体数:
    2
  • 氢受体数:
    9

文献信息

  • Use of Inhibitors of the Activity or Function of PI3K
    申请人:NOVARTIS AG
    公开号:US20150342951A1
    公开(公告)日:2015-12-03
    The invention relates to new uses of PI3K inhibitors, wherein said inhibitors have an inhibitory action on the PI3K isoform delta for the treatment of immunopathology in a subject suffering from a disease or disorder selected from malaria, leishmaniasis, trypanosomiasis, toxoplasmosis and/or neurocysticercosis, via functional inhibition of TLR9 of the infected subject.
    该发明涉及PI3K抑制剂的新用途,其中所述抑制剂PI3K同工酶δ具有抑制作用,用于治疗患有疟疾、利什曼病、锥虫病、弓形虫病和/或神经囊虫病等疾病或紊乱的受试者的免疫病理学,通过对感染受试者的TLR9的功能抑制。
  • Pyrazine Derivatives and Use as P13k Inhibitors
    申请人:Gaillard Pascale
    公开号:US20090082356A1
    公开(公告)日:2009-03-26
    The present invention is related to pyrazine derivatives of Formula (I) in particular for the treatment and/or prophylaxis of autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, bacterial or viral infections, kidney diseases, platelet aggregation, cancer, transplantation, graft rejection or lung injuries.
    本发明涉及式(I)的吡嗪生物,特别用于治疗和/或预防自身免疫性疾病和/或炎症性疾病、心血管疾病、神经退行性疾病、细菌或病毒感染、肾脏疾病、血小板聚集、癌症、移植、移植排斥或肺部损伤。
  • Methods of Using PI3K and MEK Modulators
    申请人:Aftab Dana T.
    公开号:US20100075947A1
    公开(公告)日:2010-03-25
    The invention provides methods of treating cancer with a combination of compounds which inhibit kinases, more specifically MEK and PI3K.
    本发明提供了一种使用抑制激酶的化合物组合来治疗癌症的方法,更具体地说是抑制MEK和PI3K的化合物组合。
  • Phosphatidylinositol 3-Kinase Inhibitors and Methods of Their Use
    申请人:Bajjalieh William
    公开号:US20100087440A1
    公开(公告)日:2010-04-08
    The present invention comprises small molecule inhibitors of phosphatidylinositol 3-kinase (PI3K), which is associated with a number of malignancies such as ovarian cancer, cervical cancer, breast cancer, colon cancer, rectal cancer, and glioblastomas, among others. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting these diseases.
    本发明涉及磷脂酰肌醇3-激酶(PI3K)的小分子抑制剂,该酶与多种恶性肿瘤相关,如卵巢癌、宫颈癌、乳腺癌、结肠癌、直肠癌和胶质母细胞瘤等。因此,本发明的化合物可用于治疗、预防和/或抑制这些疾病。
  • Phosphatidylinositol 3-Kinase Inhibitors And Methods Of Their Use
    申请人:Bajjalieh William
    公开号:US20110207712A1
    公开(公告)日:2011-08-25
    The present invention comprises small molecule inhibitors of phosphatidylinositol 3-kinase (PI3K), which is associated with a number of malignancies such as ovarian cancer, cervical cancer, breast cancer, colon cancer, rectal cancer, and glioblastomas, among others. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting these diseases.
    本发明涉及磷脂酰肌醇3-激酶(PI3K)的小分子抑制剂PI3K与多种恶性肿瘤相关,如卵巢癌、宫颈癌、乳腺癌、结肠癌、直肠癌和胶质母细胞瘤等。因此,本发明化合物可用于治疗、预防和/或抑制这些疾病。
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