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4,4'-(1-乙酰基-2-羰基二氢吲哚-3-亚基)二苯基二(乙酸酯) | 18869-73-3

中文名称
4,4'-(1-乙酰基-2-羰基二氢吲哚-3-亚基)二苯基二(乙酸酯)
中文别名
4,4'-(1-乙酰基-2-氧代吲哚啉-3-亚基)二苯基二(乙酸酯);三醋酚丁
英文名称
3,3-bis-(4-acetoxy-phenyl)-1-acetyl-indolin-2-one
英文别名
3,3-Bis-(4-acetoxy-phenyl)-1-acetyl-indolin-2-on;4,4'-(1-acetyl-2-oxoindolin-3-ylidene)diphenyl di(acetate);2H-Indol-2-one, 1-acetyl-3,3-bis[4-(acetyloxy)phenyl]-1,3-dihydro-;[4-[1-acetyl-3-(4-acetyloxyphenyl)-2-oxoindol-3-yl]phenyl] acetate
4,4'-(1-乙酰基-2-羰基二氢吲哚-3-亚基)二苯基二(乙酸酯)化学式
CAS
18869-73-3
化学式
C26H21NO6
mdl
——
分子量
443.456
InChiKey
JPGUEMQIAGJQSJ-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

物化性质

  • 熔点:
    201.5°C
  • 沸点:
    553.76°C (rough estimate)
  • 密度:
    1.3106 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    90
  • 氢给体数:
    0
  • 氢受体数:
    6

ADMET

毒理性
  • 药物性肝损伤
化合物:三乙酰基二苯基碘酸酯
Compound:triacetyldiphenolisatin
来源:Drug Induced Liver Injury Rank (DILIrank) Dataset
毒理性
  • 药物性肝损伤
药物性肝损伤标注:最令人关注的药物性肝损伤
DILI Annotation:Most-DILI-Concern
来源:Drug Induced Liver Injury Rank (DILIrank) Dataset
毒理性
  • 药物性肝损伤
严重程度等级:8
Severity Grade:8
来源:Drug Induced Liver Injury Rank (DILIrank) Dataset
毒理性
  • 药物性肝损伤
标签部分:已撤回
Label Section:Withdrawn
来源:Drug Induced Liver Injury Rank (DILIrank) Dataset
毒理性
  • 药物性肝损伤
参考文献:M Chen, V Vijay, Q Shi, Z Liu, H Fang, W Tong. 用于研究药物诱导肝损伤的FDA批准药物标签,药物发现今日,16(15-16):697-703, 2011. PMID:21624500 DOI:10.1016/j.drudis.2011.05.007 M Chen, A Suzuki, S Thakkar, K Yu, C Hu, W Tong. DILIrank:按在人类中发展药物诱导肝损伤风险排名的最大参考药物清单。药物发现今日2016, 21(4): 648-653. PMID:26948801 DOI:10.1016/j.drudis.2016.02.015
References:M Chen, V Vijay, Q Shi, Z Liu, H Fang, W Tong. FDA-Approved Drug Labeling for the Study of Drug-Induced Liver Injury, Drug Discovery Today, 16(15-16):697-703, 2011. PMID:21624500 DOI:10.1016/j.drudis.2011.05.007 M Chen, A Suzuki, S Thakkar, K Yu, C Hu, W Tong. DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans. Drug Discov Today 2016, 21(4): 648-653. PMID:26948801 DOI:10.1016/j.drudis.2016.02.015
来源:Drug Induced Liver Injury Rank (DILIrank) Dataset

安全信息

  • 海关编码:
    2933790090

制备方法与用途

类别:有毒物品

毒性分级:高毒

急性毒性:

  • 口服(大鼠)LD50:500 毫克/公斤
  • 腹腔(大鼠)LD50:350 毫克/公斤

可燃性危险特性:可燃;加热分解时释放有毒氮氧化物和氯化物烟雾

储运特性:库房通风、低温干燥

灭火剂:干粉、泡沫、砂土、二氧化碳、雾状水

反应信息

点击查看最新优质反应信息

文献信息

  • Easy-cleavage shrink laminate film and the bag using the same
    申请人:Idemitsu Petrochemical Co., Ltd.
    公开号:EP0903220A2
    公开(公告)日:1999-03-24
    Disclosed are an easy-cleavage shrink laminate film which is harmless to the environment, easy to tear and moderately shrinkable, and a bag made of the laminate film. The easy-cleavage shrink laminate film 22 has a basic, two-layered structure composed of an easy-cleavage shrink film 19 and a sealant film 21, and may optionally comprise an additional sealant film 21 and/or a substrate film 25 to have a multi-layered structure. The easy-cleavage shrink film 19 comprises from 40 to 85 parts by weight of Ny 6 and from 15 to 60 parts by weight of MXD 6, and this is drawn at an orientation ratio of not smaller than 2.8 times both in the MD direction and in the TD direction and thermally fixed at a heat-treating temperature falling between 120 and 195°C to thereby have a degree of shrinkage of from 15 to 40 % when it is put in hot water at 120°C under pressure of about 2.0 kg/cm2 for 20 minutes.
    本发明公开了一种对环境无害、易撕裂和适度收缩的易撕收缩复合膜,以及一种由该复合膜制成的袋子。易撕裂收缩复合膜 22 具有基本的两层结构,由易撕裂收缩膜 19 和密封膜 21 组成,也可选择包括额外的密封膜 21 和/或基材膜 25 以形成多层结构。易撕裂收缩膜 19 由 40 至 85 重量份的 Ny 6 和 15 至 60 重量份的 MXD 6 组成,以不小于 2.8 倍的取向比在 MD 方向和 TD 方向拉伸,并在 120 至 195°C 的热处理温度下进行热固定,从而在压力约为 2.0 kg/cm2 的情况下将其放入 120°C 的热水中 20 分钟,收缩率为 15 至 40%。
  • PHARMACEUTICAL COMPOSITION CONTAINING A CENTRAL OPIOID AGONIST, A CENTRAL OPIOID ANTAGONIST, AND A PERIPHERAL OPIOID ANTAGONIST, AND METHOD FOR MAKING THE SAME
    申请人:Harrogate Holdings
    公开号:EP1981502A2
    公开(公告)日:2008-10-22
  • Pharmaceutical composition containing a central opioid agonist, a central opioid antagonist, and a peripheral opioid antagonist, and method for making the same
    申请人:Royds B. Robert
    公开号:US20070185145A1
    公开(公告)日:2007-08-09
    A pharmaceutical composition for treating or preventing a disease, condition or symptoms thereof in a warm-blooded animal including a human, includes a therapeutically effective amount of an opioid agonist exhibiting potential pharmacologically addictive properties in warm blooded animals including humans; a side-effect reducing agent present in amounts sufficient to at least substantially neutralize the adverse side effects of the opioid agonist; an opioid antagonist present in a sequestered form in amounts sufficient to block the pharmacological effect of the opioid agonist upon release from the sequestered form; and a pharmaceutically acceptable carrier.
  • Heat-accumulating heater
    申请人:Komiya Kunihiko
    公开号:US20090229593A1
    公开(公告)日:2009-09-17
    A heat-accumulating heater includes a powdery paraffinic latent heat storage substance sealed in a bag-shaped container. The bag-shaped container includes a plurality of inner container members formed of sheets impermeable to the heat storage substance and water and permeable to air. The inner container members are each received in one of first substantially rectangular outer container members made of rubber that are connected to each other in a row so as to be bendable relative to each other. An air layer is present between each inner container member and the corresponding first outer container member, thereby preventing the inner container member from being pressed against the first outer container member. The first outer container members are in turn received in a second outer container member made of cloth.
  • METHOD AND COMPOSITION FOR A SACHA INCHI PERENNIAL PLANT EXTRACT BASED HEALTH AND BEAUTY AID
    申请人:TRI-K Industries, Inc.
    公开号:US20180280287A1
    公开(公告)日:2018-10-04
    A method and composition for non-invasive treatment of skin aging conditions utilizes a topically applied composition that includes a sustainable non GMO water based extract of peptide Sacha Inchi (hydrolyzed Plukenetia Volubilis Seed Extract). The composition utilizes Sacha Inchi to clinically and non-invasively reduce after only 28 days skin sagginess and facial volume contour. Reshaping and resculpting facial skin and reducing dermal non-echogenic surfaces are also accomplished. Increased echogenic surfaces, increased dermal connective tissue and dermal density by restructuring, re-densifying and revitalizing dermis for healthier skin is furthered. The composition was clinically proven to reduce after only 21 days of treatment fine lines, deep wrinkles and facial skin roughness, for a smoother, healthier, younger and less wrinkled skin. The composition was also clinically proven to reduce sebum production, minimize pore size, mattifying skin appearance by sebum regulation and smoothing the appearance of skin after only 21 days of treatment.
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