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2-cyano-3-(4-nitrophenyl)-N-[(1R)-1-phenylethyl]prop-2-enamide

中文名称
——
中文别名
——
英文名称
2-cyano-3-(4-nitrophenyl)-N-[(1R)-1-phenylethyl]prop-2-enamide
英文别名
——
2-cyano-3-(4-nitrophenyl)-N-[(1R)-1-phenylethyl]prop-2-enamide化学式
CAS
——
化学式
C18H15N3O3
mdl
——
分子量
321.3
InChiKey
RYYNDHCHTCVQJH-CYBMUJFWSA-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):
    3.3
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    98.7
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Natural-killer/T-cell lymphoma (NKTCL) susceptibility prediction, diagnosis and therapy
    申请人:SINGAPORE HEALTH SERVICES PTE LTD
    公开号:US10378062B2
    公开(公告)日:2019-08-13
    Natural-KilleifT-Cell Lymphoma (NKTCL) susceptibility prediction, diagnosis and therapy. The invention relates to a method for predicting Natural Killer T-cell Lymphoma (NKTCL) susceptibility and/or diagnosing NKTCL in a subject comprising testing for JAK mutations. The invention also relates to a method of screening for candidate agents capable of treating NKTCL using a cell line comprising at least one JAK mutation. The invention includes an NKTCL animal model comprising at least one JAK mutation. The invention also includes JAK inhibitors for treating NKTCL.
    天然杀伤T细胞淋巴瘤(NKTCL)易感性预测、诊断和治疗。本发明涉及一种预测天然杀伤T细胞淋巴瘤(NKTCL)易感性和/或诊断受试者NKTCL的方法,包括检测JAK突变。本发明还涉及一种利用包含至少一种 JAK 突变的细胞系筛选能够治疗 NKTCL 的候选药物的方法。本发明包括一种包含至少一种 JAK 突变的 NKTCL 动物模型。本发明还包括用于治疗NKTCL的JAK抑制剂
  • EP2782562A2
    申请人:——
    公开号:EP2782562A2
    公开(公告)日:2014-10-01
  • NATURAL-KILLER/T-CELL LYMPHOMA (NKTCL) SUSCEPTIBILITY PREDICTION, DIAGNOSIS AND THERAPY
    申请人:Singapore Health Services Pte Ltd
    公开号:EP2782562B1
    公开(公告)日:2016-12-21
  • METHODS OF TREATING DERMATOLOGIC, GYNECOLOGIC, AND GENITAL DISORDERS WITH CAFFEIC ACID ANALOGS
    申请人:Priebe Anna
    公开号:US20110275577A1
    公开(公告)日:2011-11-10
    The present invention relates to caffeic acid analog compounds and methods which may be useful for regeneration, cellular programming, and the treatment of dermatologic, gynecologic, and genital diseases such as inflammatory dermatologic conditions, dysplasia, neoplasia, in situ carcinoma, invasive carcinoma, lichen sclerosus, lichen planus, vaginal dysplasia, vaginal carcinoma, vulvar dysplasia, vulvar carcinoma, cervical dysplasia, cervical carcinoma, and Kaposi's sarcoma.
  • INTERFERON THERAPIES IN COMBINATION WITH BLOCKADE OF STAT3 ACTIVATION
    申请人:Priebe Waldemar
    公开号:US20130129675A1
    公开(公告)日:2013-05-23
    Methods of modulating the INF-induced STAT3 activation in a patient in need-thereof are provided for the treatment of disease. The methods comprise the step of administrating to a patient the combination of a therapeutically effective amount of interferon including INF-α and/or INF-β in combination with a STAT3 inhibitor.
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