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4-[(2S)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile | 1159489-36-7

中文名称
——
中文别名
——
英文名称
4-[(2S)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile
英文别名
4-[(2S)-2-amino-2-cyanoethyl]-3-fluorobenzonitrile
4-[(2S)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile化学式
CAS
1159489-36-7
化学式
C10H8FN3
mdl
——
分子量
189.192
InChiKey
GDXANENQFUEUCO-VIFPVBQESA-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):
    0.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    73.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    N-{(1S)-1-[2'-chloro-4'-(methylsulfonyl)biphenyl-4-yl]-2,2,2-trifluoro-ethyl}-4-fluoro-L-leucine 、 4-[(2S)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile 生成 (S)-2-[(S)-1-[2'-chloro-4'-(methanesulfonyl)-biphenyl-4-yl]-2,2,2-trifluoro-ethylamino]-4-fluoro-4-methyl-pentanoic acid [1-cyano-2-(2-fluoro-4-cyano-phenyl)-ethyl]-amide
    参考文献:
    名称:
    Cysteine protease inhibitors for the treatment of parasitic diseases
    摘要:
    一些导致哺乳动物疾病的寄生虫依赖半胱氨酸蛋白酶进行各种生命周期功能。抑制或降低这些蛋白酶的功能可以在治疗和/或预防这些寄生虫病,包括弓形虫病、疟疾、非洲锥虫病、恙虫病、利什曼病、血吸虫病、阿米巴病、贾第虫病、华支睾吸虫病、华支睾吸虫病、肺吸虫病、巨吸虫病、淋巴丝虫病、昆虫体内丝虫病、龙虫病、蛔虫病、鞭虫病、强蛔虫病、阴道滴虫病或绦虫病中有用。
    公开号:
    US08642799B2
  • 作为产物:
    描述:
    4-{2-cyano-2-[(diphenylmethylene)amino]ethyl}-3-fluorobenzonitrile 在 溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 生成 4-[(2S)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile 、 4-[(2R)-(2-amino-2-cyanoethyl)]-3-fluorobenzonitrile
    参考文献:
    名称:
    Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease
    摘要:
    Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease is described. The identified inhibitors bearing an amino nitrile warhead in P1 exhibit low nanomolar in vitro potency against cruzipain. Further SAR in P2 portion led to the identification of compounds, such as 26, that have a unique selectivity profile against other cysteine proteases and offering new opportunities for safer treatment of Chagas disease. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.10.015
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文献信息

  • [EN] CYSTEINE PROTEASE INHIBITORS FOR THE TREATMENT OF PARASITIC DISEASES<br/>[FR] INHIBITEURS DE CYSTÉINE-PROTÉASES POUR LE TRAITEMENT DE MALADIES PARASITAIRES
    申请人:MERCK FROSST CANADA LTD
    公开号:WO2009067797A1
    公开(公告)日:2009-06-04
    Several parasites responsible for mammalian diseases are dependent on cysteine protease for various life-cycle functions. Inhibition or decreasing function of these proteases can be useful in the treatment and/or prevention of these parasitic diseases including; toxoplasmosis, malaria, African trypanosomiasis, Chagas disease, leishmaniasis, schistosomiasis, amebiasis, giardiasis, clonorchiasis, opisthorchiasis, paragonimiasis, fasciolopsiasis, lymphatic filariasis, onchocerciasis, dracunculiasis, ascariasis, trichuriasis, strongyloidiasis, trichostrongyliasis, trichomoniasis or cestodiasis. Compounds of formula I of the invention are capable of treating and/or preventing the above-identified diseases:
    一些导致哺乳动物疾病的寄生虫依赖半胱氨酸蛋白酶进行各种生命周期功能。抑制或减少这些蛋白酶的功能可以在治疗和/或预防包括弓形虫病、疟疾、非洲锥虫病、克氏病、利什曼病、血吸虫病、阿米巴病、贾第虫病、华支睾吸虫病、华支睾吸虫病、肺吸虫病、淋巴丝虫病、显微丝虫病、蛔虫病、鞭虫病、强力虫病、毛圆线虫病、滴虫病或绦虫病等寄生虫病方面发挥作用。本发明的I类化合物能够治疗和/或预防上述疾病。
  • CYSTEINE PROTEASE INHIBITORS FOR THE TREATMENT OF PARASITIC DISEASES
    申请人:ISABEL Elise
    公开号:US20130244962A1
    公开(公告)日:2013-09-19
    Several parasites responsible for mammalian diseases are dependent on cysteine protease for various life-cycle functions. Inhibition or decreasing function of these proteases can be useful in the treatment and/or prevention of these parasitic diseases including; toxoplasmosis, malaria, African trypanosomiasis, Chagas disease, leishmaniasis, schistosomiasis, amebiasis, giardiasis, clonorchiasis, opisthorchiasis, paragonimiasis, fasciolopsiasis, lymphatic filariasis, onchocerciasis, dracunculiasis, ascariasis, trichuriasis, stronglyoidiasis, trichostrongyliasis, trichomoniasis or cestodiasis.
    许多导致哺乳动物疾病的寄生虫依赖于半胱氨酸蛋白酶进行各种生命周期功能。抑制或降低这些蛋白酶的功能可以在治疗和/或预防这些寄生虫病方面发挥作用,包括弓形虫病、疟疾、非洲锥虫病、恙虫病、利什曼病、血吸虫病、阿米巴病、贾第鞭毛虫病、华支睾吸虫病、华支睾吸虫病、肺吸虫病、广篇吸虫病、淋巴丝虫病、昆虫媒介的皮下丝虫病、龙线虫病、蛔虫病、鞭虫病、强蛔虫病、阴道毛滴虫病或绦虫病。
  • CYSTEINE PROTEASE INHIBITORS FOR THE TREATMENT OF PARASITIC DISEASE
    申请人:Isabel Elise
    公开号:US20100305056A1
    公开(公告)日:2010-12-02
    Several parasites responsible for mammalian diseases are dependent on cysteine protease for various life-cycle functions. Inhibition or decreasing function of these proteases can be useful in the treatment and/or prevention of these parasitic diseases including; toxoplasmosis, malaria, African trypanosomiasis, Chagas disease, leishmaniasis, schistosomiasis, amebiasis, giardiasis, clonorchiasis, opisthorchiasis, paragonimiasis, fasciolopsiasis, lymphatic filariasis, onchocerciasis, dracunculiasis, ascariasis, trichuriasis, strongyloidiasis, trichostrongyliasis, trichomoniasis or cestodiasis. Compounds of formula I of the invention are capable of treating and/or preventing the above-identified diseases:
    一些导致哺乳动物疾病的寄生虫依赖半胱氨酸蛋白酶进行不同的生命周期功能。抑制或减少这些蛋白酶的功能可以用于治疗和/或预防这些寄生虫病,包括弓形虫病、疟疾、非洲锥虫病、恙虫病、利什曼病、血吸虫病、阿米巴病、贾第鞭毛虫病、华支睾吸虫病、华支睾吸虫病、肺吸虫病、巨吸虫病、淋巴丝虫病、眼虫病、蛔虫病、鞭虫病、弓形虫病。本发明的I式化合物能够治疗和/或预防上述疾病。
  • US8642799B2
    申请人:——
    公开号:US8642799B2
    公开(公告)日:2014-02-04
  • Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease
    作者:Christian Beaulieu、Elise Isabel、Angélique Fortier、Frédéric Massé、Christophe Mellon、Nathalie Méthot、Momar Ndao、Deborah Nicoll-Griffith、Doris Lee、Hyeram Park、W. Cameron Black
    DOI:10.1016/j.bmcl.2010.10.015
    日期:2010.12
    Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease is described. The identified inhibitors bearing an amino nitrile warhead in P1 exhibit low nanomolar in vitro potency against cruzipain. Further SAR in P2 portion led to the identification of compounds, such as 26, that have a unique selectivity profile against other cysteine proteases and offering new opportunities for safer treatment of Chagas disease. (C) 2010 Elsevier Ltd. All rights reserved.
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