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5-(2-benzylsulfanyl-4-chloro-pyrazolo[1,5-a][1,3,5]triazin-8-yl)-pentanenitrile | 1011470-73-7

中文名称
——
中文别名
——
英文名称
5-(2-benzylsulfanyl-4-chloro-pyrazolo[1,5-a][1,3,5]triazin-8-yl)-pentanenitrile
英文别名
5-(2-benzylsulfanyl-4-chloropyrazolo[1,5-a][1,3,5]triazin-8-yl)pentanenitrile
5-(2-benzylsulfanyl-4-chloro-pyrazolo[1,5-a][1,3,5]triazin-8-yl)-pentanenitrile化学式
CAS
1011470-73-7
化学式
C17H16ClN5S
mdl
——
分子量
357.867
InChiKey
GADZYJKFSRPXNO-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):
    4.2
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    92.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities
    摘要:
    A series of macrocyclic derivatives has been designed and synthesized based on the X-ray co-crystal structures of pyrazolo[1,5-a] [1,3,5]triazines with corn CK2 (cCK2) protein. Bioassays demonstrated that these macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds are potent CK2 inhibitors with K-i around 1.0 nM and strongly inhibit cancer cell growth with IC50 as low as similar to 100 nM. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.11.074
  • 作为产物:
    描述:
    5-(2-benzylsulfanyl-4-hydroxy-pyrazolo[1,5-a][1,3,5]triazin-8-yl)-pentanenitrile 在 N,N-二甲基苯胺三氯氧磷 作用下, 反应 1.0h, 生成 5-(2-benzylsulfanyl-4-chloro-pyrazolo[1,5-a][1,3,5]triazin-8-yl)-pentanenitrile
    参考文献:
    名称:
    Protein Kinase Inhibitors
    摘要:
    嘌呤和三嗪基化学化合物,例如作为蛋白激酶抑制剂用于治疗癌症、神经系统疾病、自身免疫性疾病和其他疾病,以及使用这些化合物的方法。
    公开号:
    US20080070893A1
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文献信息

  • Protein Kinase Inhibitors
    申请人:Chu Shaosong
    公开号:US20080070893A1
    公开(公告)日:2008-03-20
    Pyrimidine- and triazine-based chemical compounds that are useful, for example, as protein kinase inhibitors for treating cancer, neurological disorders, autoimmune disorders, and other diseases, and methods of using such compounds
    嘌呤和三嗪基化学化合物,例如作为蛋白激酶抑制剂用于治疗癌症、神经系统疾病、自身免疫性疾病和其他疾病,以及使用这些化合物的方法。
  • PROTEIN KINASE INHIBITORS
    申请人:Chu Shaosong
    公开号:US20090247501A1
    公开(公告)日:2009-10-01
    Pyrimidine- and triazine-based chemical compounds that are useful, for example, as protein kinase inhibitors for treating cancer, neurological disorders, autoimmune disorders, and other diseases, and methods of using such compounds
    嘌呤和三嗪基化学化合物,例如作为蛋白激酶抑制剂用于治疗癌症、神经系统疾病、自身免疫疾病和其他疾病,以及使用这些化合物的方法。
  • Protein kinase inhibitors
    申请人:Polaris Group
    公开号:US07517882B2
    公开(公告)日:2009-04-14
    Pyrimidine- and triazine-based chemical compounds that are useful, for example, as protein kinase inhibitors for treating cancer, neurological disorders, autoimmune disorders, and other diseases, and methods of using such compounds.
    嘌呤和三嗪基化合物,例如作为蛋白激酶抑制剂用于治疗癌症、神经系统疾病、自身免疫性疾病和其他疾病,以及使用这些化合物的方法。
  • Pyrazolo[l,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives useful as protein kinase inhibitors
    申请人:Polaris Group
    公开号:EP2064214B1
    公开(公告)日:2013-01-30
  • US7517882B2
    申请人:——
    公开号:US7517882B2
    公开(公告)日:2009-04-14
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同类化合物

酪氨酸,2-甲氧基-O-甲基- 达美司特 百里酚-6-磺化三(2-羟基乙基)铵 吡唑并[1,5-a][1,3,5]噻嗪-4(3H)-酮 吡唑并[1,5-a][1,3,5]三嗪-2,4-二胺 吡唑并[1,5-D][1,2,4]三嗪酮 吡唑并[1,5-A]-1,3,5-三嗪-2,4(1H,3H)-二酮 N4-(1,1-二甲基乙基)-7-甲基吡唑并(1,5-a)-1,3,5-三嗪-2,4-二胺盐酸盐 N'-甲酰基-4-氨基吡唑并[5,1-c][1,2,4]三嗪-3-甲酰肼 8-苄基-2-甲基-4-(N-甲基氨基)吡唑并[1,5-a]-1,3,5-三嗪 8-溴-4-氯-2-(甲基硫代)吡唑并[1,5-a][1,3,5]三嗪 7-甲基-6H-吡唑并[4,5-e][1,2,3]三嗪-4-酮 7-甲基-1,7-二氢-4H-吡唑并[3,4-d][1,2,3]三嗪-4-酮2-氧化物 7-(叔丁基)吡唑并[1,5-a][1,3,5]三嗪-4(3H)-酮 5,6-二氢吡唑并[1,5-d][1,2,4]三嗪-4,7-二酮 4-甲氧基吡唑并[1,5-a][1,3,5]三嗪 4-氯-2-(甲硫基)吡唑并[1,5-a][1,3,5]三嗪 4-氨基-7-甲基吡唑并[5,1-C][1,2,4]三嗪-3-甲腈 4,7-二甲基吡唑并[5,1-c][1,2,4]三嗪-3-羧酸乙酯 4,7-二甲基吡唑并[5,1-C][1,2,4]三嗪-3-羧酸 4,6-二氢-6-(碘乙酰基)-3-甲基-4-亚甲基吡唑并[5,1-c][1,2,4]三嗪 3-甲氧基-2H-吡唑并[4,3-e][1,2,4]三嗪 3-(1,1-二甲基乙基)-7-(5-甲基-3-异恶唑基)-2-[(1-甲基-1H-1,2,4-三唑-5-基)甲氧基]吡唑并[1,5-d][1,2,4]三嗪 3,4-二甲基吡唑并[5,1-c][1,2,4]三嗪 2-甲基吡唑并[1,5-d][1,2,4]三嗪-4(5H)-酮 2-甲基-4-(N-甲基氨基)-8-[(2-噻吩基)甲基]吡唑并[1,5-a]-1,3,5-三嗪 2-Thi氧代-2,3-二氢吡唑并[1,5-a][1,3,5]噻嗪-4(1H)-酮 2-(甲基硫代)吡唑并[1,5-a][1,3,5]噻嗪-4(3H)-酮 2,4-二氨基-吡唑并(1,5-a)-S-三嗪盐酸盐半水合物 2,4-二(甲基氨基)-7-甲基吡唑并(1,5-a)-S-三嗪 1-(4,7-二甲基吡唑并[5,1-c][1,2,4]三氮杂-3-基)-1-乙酮 4-(2,4-dichlorophenyl)-8-(3-pentyl)-7-ethyl-2-methyl-pyrazolo[1,5-a]-1,3,5-triazine 2-(4-tert-butylphenyl)-4-({3-[(2,3-dihydro-1H-inden-2-yl)amino]-2,2-difluoropropyl}amino)-6H,7H-pyrazolo[1,5-a][1,3,5]triazin-7-one 2-(4-tert-butylphenyl)-4-{[3-(dimethylamino)propyl]amino}-8-[(6-methylpyridin-3-yl)methyl]-6H,7H-pyrazolo[1,5-a][1,3,5]triazin-7-one 4-methyl-N-(1-methyl-1-phenylethyl)-2-phenyl-1,2,3,4-tetrahydropyrazolo[5,1-c][1,2,4]triazine-8-carboxamide 2,4-diphenyl-pyrazolo[1,5-a][1,3,5]triazine 3H-8-carbonitrile-2-(5-chlorouracil-6-methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)-7-tert-butylpyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)-7-methylpyrazolo[1,5-a][1,3,5]triazin-4-one 3H-8-carboxylic acid ethyl ester 2-(5-chlorouracil-6-methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)-7-trifluoromethylpyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)-8-methylpyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-one 3H-2-(5-chlorouracil-6-methylthio)-8-iodopyrazolo[1,5-a][1,3,5]triazin-4-one 3H-8-chloro-2-(5-chlorouracil-6-methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-one 3H-8-bromo-2-(5-chlorouracil-6-methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-one 6-[4-(1-hydroxy-1-methylethyl)phenyl]-2-methyl-5H-1,5,7,7a-tetraazainden-4-one Pyrazolo<3,2-f><1,2,4>triazin-4(3H)-on methyl 3,7-dimethyl-4-oxo-4,6-dihydro-pyrazolo[5,1-c][1,2,4]triazine-8-carboxylate 2-(4-tert-butylphenyl)-4-{[3-(4-chloro-3-methylphenoxy)propyl]sulfanyl}-6H,7H-pyrazolo[1,5-a] [1,3,5]triazin-7-one