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1-[3-(trifluoromethyl)phenyl]-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate

中文名称
——
中文别名
——
英文名称
1-[3-(trifluoromethyl)phenyl]-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate
英文别名
——
1-[3-(trifluoromethyl)phenyl]-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate化学式
CAS
——
化学式
C19H15F3N2O2
mdl
MFCD02059128
分子量
360.3
InChiKey
BCAAQHIVHZXLCQ-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):
    1.4
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    65.1
  • 氢给体数:
    3
  • 氢受体数:
    6

文献信息

  • [EN] CARBOLINE AND BETACARBOLINE DERIVATIVES FOR USE AS HDAC ENZYME INHIBITORS<br/>[FR] DERIVES DE CARBOLINE ET DE BETACARBOLINE INHIBITEURS DE L'ENZYME HDAC
    申请人:CHROMA THERAPEUTICS LTD
    公开号:WO2004113336A1
    公开(公告)日:2004-12-29
    Compounds of formula (IA) and (IB) are inhibitors of histone deacetylase activity and useful for the treatment of, inter alia, cancers: wherein fused rings A1 and A2 are optionally substituted; linker radical R1 represents a radical of formula
    式(IA)和(IB)的化合物是组蛋白去乙酰化酶活性的抑制剂,用于治疗癌症等疾病:其中融合的环A1和A2可以选择性地被取代;连接基团R1代表一个公式的基团。
  • IDO Inhibitors
    申请人:Mautino Mario
    公开号:US20110053941A1
    公开(公告)日:2011-03-03
    Presently provided are methods for (a) modulating an activity of indoleamine 2,3-dioxygenase comprising contacting an indoleamine 2,3-dioxygenase with a modulation effective amount of a compound as described in one of the aspects described herein; (b) treating indoleamine 2,3-dioxygenase (IDO) mediated immunosuppression in a subject in need thereof, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (c) treating a medical conditions that benefit from the inhibition of enzymatic activity of indoleamine-2,3-dioxygenase comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (d) enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent and a compound as described in one of the aspects described herein; (e) treating tumor-specific immunosuppression associated with cancer comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; and (f) treating immunosuppression associated with an infectious disease, e.g., HIV-I infection, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount a compound as described in one of the aspects described herein.
    目前提供以下方法:(a) 通过接触本文中描述的化合物的调节有效量与吲哚胺2,3-二氧化酶相互作用,从而调节吲哚胺2,3-二氧化酶的活性;(b) 治疗需要吲哚胺2,3-二氧化酶(IDO)介导的免疫抑制的患者,包括给予本文中描述的化合物的有效吲哚胺2,3-二氧化酶抑制剂量;(c) 治疗需要抑制吲哚胺-2,3-二氧化酶酶活性的医疗状况,包括给予本文中描述的化合物的有效吲哚胺2,3-二氧化酶抑制剂量;(d) 增强抗癌治疗的有效性,包括给予抗癌剂和本文中描述的化合物;(e) 治疗与癌症相关的肿瘤特异性免疫抑制,包括给予本文中描述的化合物的有效吲哚胺2,3-二氧化酶抑制剂量;(f) 治疗与传染病相关的免疫抑制,例如HIV-1感染,包括给予本文中描述的化合物的有效吲哚胺2,3-二氧化酶抑制剂量。
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