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2-acetamido-5-phenoxy thiophene | 190967-00-1

中文名称
——
中文别名
——
英文名称
2-acetamido-5-phenoxy thiophene
英文别名
N-(5-phenoxythiophen-2-yl)acetamide
2-acetamido-5-phenoxy thiophene化学式
CAS
190967-00-1
化学式
C12H11NO2S
mdl
——
分子量
233.291
InChiKey
FALJLPFFINOHSD-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):
    3
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    66.6
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    2-acetamido-5-phenoxy thiopheneammonium hydroxidelithium diisopropyl amide 作用下, 以 甲醇 为溶剂, 反应 1.75h, 生成 N-[5Phenoxythien-2-yl]isopropylsulfonamide
    参考文献:
    名称:
    N-(5-substituted) thiophene-2-alkylsulfonamides as potent inhibitors of 5-lipoxygenase
    摘要:
    Compound 4k N-[5-(4-fluoro) phenoxythien-2-yl] methanesulfonamide is representative of a new class of potent inhibitors of 5-lipoxygenase (5-LO). These versatile compounds exhibit dose-dependent inhibition of 5-LO with IC(50)s ranging from 20-100 nM in the rat basophilic leukemia (RBL-1) cell homogenate assay and submicromolar IC,,s in both the RBL-1 and human peripheral blood leukocyte (PBL) whole cell assays. Compound 4k also showed significant anti-inflammatory activity in the adjuvant arthritic rat at an oral dose of 3 mg/kg. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(97)00025-4
  • 作为产物:
    描述:
    苯酚 、 alkaline earth salt of/the/ methylsulfuric acid 在 铁粉potassium carbonate溶剂黄146 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 生成 2-acetamido-5-phenoxy thiophene
    参考文献:
    名称:
    N-(5-substituted) thiophene-2-alkylsulfonamides as potent inhibitors of 5-lipoxygenase
    摘要:
    Compound 4k N-[5-(4-fluoro) phenoxythien-2-yl] methanesulfonamide is representative of a new class of potent inhibitors of 5-lipoxygenase (5-LO). These versatile compounds exhibit dose-dependent inhibition of 5-LO with IC(50)s ranging from 20-100 nM in the rat basophilic leukemia (RBL-1) cell homogenate assay and submicromolar IC,,s in both the RBL-1 and human peripheral blood leukocyte (PBL) whole cell assays. Compound 4k also showed significant anti-inflammatory activity in the adjuvant arthritic rat at an oral dose of 3 mg/kg. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(97)00025-4
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文献信息

  • 2,5-disubstituted thiophenes: inhibitors of 5-lipoxygenase and inducible
    申请人:Ortho Pharmaceutical Corporation
    公开号:US05783597A1
    公开(公告)日:1998-07-21
    2,5-Disubstituted thiophene derivatives, and more particularly, to 2-aryloxy-5-alkansulfonamido-thiophenes of the general formula: ##STR1## Wherein, R.sub.2 is CF.sub.3, C.sub.1 -C.sub.10 alkyl, or phenyl; X is O, S, or CH.sub.2 ; and R is aryl, C.sub.1 -C.sub.10 alkyl, or C.sub.3 -C.sub.8 cycloalkyl; which compounds are pharmacologically active in alleviating inflammation, asthma, arthritis, hypersensitivity, myocardial ischemia and dermatological conditions, such as, psoriasis and dermatitis, and gastrointestinal inflammatory conditions, such as, inflammatory bowel syndrome.
    本发明涉及2,5-二取代噻吩生物,更具体地,涉及通式为:##STR1##的2-芳氧基-5-烷基磺酰胺基噻吩。其中,R.sub.2为CF.sub.3,C.sub.1-C.sub.10烷基或苯基;X为O,S或CH.sub.2;R为芳基,C.sub.1-C.sub.10烷基或C.sub.3-C.sub.8环烷基。这些化合物在缓解炎症、哮喘、关节炎、过敏、心肌缺血和皮肤病(如牛皮癣和皮炎)以及胃肠道炎症状况(如炎性肠病)方面具有药理活性。
  • US5783597A
    申请人:——
    公开号:US5783597A
    公开(公告)日:1998-07-21
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