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2-(3-甲酰基-2-甲基-1H-吲哚-1-基)乙酰胺 | 61922-00-7

中文名称
2-(3-甲酰基-2-甲基-1H-吲哚-1-基)乙酰胺
中文别名
2-(3-甲酰-2-甲基-1H-吲哚-1-基)乙酰胺
英文名称
2-(3-formyl-2-methyl-indol-1-yl)-acetamide
英文别名
2-methyl-3-formyl-1-indoleacetamide;3-Formyl-2-methylindol-1-acetamid;2-(3-Formyl-2-methyl-1H-indol-1-yl)acetamide;2-(3-formyl-2-methylindol-1-yl)acetamide
2-(3-甲酰基-2-甲基-1H-吲哚-1-基)乙酰胺化学式
CAS
61922-00-7
化学式
C12H12N2O2
mdl
MFCD02197474
分子量
216.239
InChiKey
YPMNUMFCLRBFHC-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):
    0.9
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    65.1
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933990090
  • WGK Germany:
    3

SDS

SDS:0529b20188761fff9606529cab3846bd
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-甲基吲哚-3-甲醛氯乙酰胺 以 (2S)-N-methyl-1-phenylpropan-2-amine hydrate 、 N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 生成 2-(3-甲酰基-2-甲基-1H-吲哚-1-基)乙酰胺
    参考文献:
    名称:
    2-Substituted-indole-1-lower-alkanecarboxamides
    摘要:
    2-取代吲哚-1-低烷基羧酰胺,通过相应酸或酯的酰胺化制备;通过相应碳腈的水解或硫水解;通过将适当的吲哚与卤代低烷基羧酰胺烷基化;或通过对1-吲哚氯磺酰氨基衍生物的水解,具有抗分泌和抗溃疡活性。
    公开号:
    US04021448A1
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文献信息

  • [EN] INDOLINIUM-DERIVED THIOL/DISULFIDE DYE, DYE COMPOSITION COMPRISNG THIS DYE, PROCESS FOR LIGHTENING KERATIN MATERIALS USING THIS DYE<br/>[FR] COLORANT THIOL/DISULFURE DÉRIVÉ D'INDOLIUM, COMPOSITION COLORANTE COMPRENANT LEDIT COLORANT, PROCÉDÉ D'ÉCLAIRCISSEMENT DE MATÉRIAUX À BASE DE KÉRATINE AU MOYEN DE CE COLORANT
    申请人:OREAL
    公开号:WO2009037348A1
    公开(公告)日:2009-03-26
    The invention relates to the dyeing of keratin materials using indolinium-derived thiol and disulfide fluorescent dyes. The invention relates to a dye composition comprising an indolinium-derived-chromophore thiol or disulfide dye and to a dyeing process with a lightening effect on keratin fibers such as the hair, using said composition. It similarly relates to novel indolinium-derived-chromophore thiol dyes and to the uses thereof in lightening keratin materials. This composition makes it possible to obtain a coloring with a lightening effect which is particularly resistant and visible on dark keratin fibers.
    该发明涉及使用吲哚啉衍生硫醇和二硫化物荧光染料对角蛋白材料进行染色。该发明涉及一种染料组合物,包括一种吲哚啉衍生色团硫醇或二硫化物染料,以及使用该组合物对角蛋白纤维(如头发)进行具有减淡效果的染色过程。它还涉及新型吲哚啉衍生色团硫醇染料及其在减淡角蛋白材料中的用途。该组合物能够实现一种具有减淡效果的染色,特别是在深色角蛋白纤维上表现出耐久性和可见性。
  • 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。
  • Bi-functional complexes and methods for making and using such complexes
    申请人:Gouliaev Alex Haahr
    公开号:US11225655B2
    公开(公告)日:2022-01-18
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
    本发明涉及一种合成双功能复合物的方法,该复合物包括分子部分和识别分子部分的识别寡核苷酸部分。根据本发明的合成方法的一部分优选在一种或多种有机溶剂中进行,此时包含可选保护标签或寡核苷酸标识符的新生双功能复合物与固体支持物相连接,合成方法的另一部分优选在适合于将寡核苷酸标签酶加到溶液中的新生双功能复合物的条件下进行。
  • BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Nuevolution A/S
    公开号:EP2558577A1
    公开(公告)日:2013-02-20
  • BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Gouliaev Alex Haahr
    公开号:US20130281324A1
    公开(公告)日:2013-10-24
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
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