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3-(3-(5-hexenyloxy)-1,2,5-thiadiazol-4-yl)pyridine | 131987-85-4

中文名称
——
中文别名
——
英文名称
3-(3-(5-hexenyloxy)-1,2,5-thiadiazol-4-yl)pyridine
英文别名
3-(4-(5-hexenyloxy)-1,2,5-thiadiazol-3-yl)pyridine;3-hex-5-enoxy-4-pyridin-3-yl-1,2,5-thiadiazole
3-(3-(5-hexenyloxy)-1,2,5-thiadiazol-4-yl)pyridine化学式
CAS
131987-85-4
化学式
C13H15N3OS
mdl
——
分子量
261.348
InChiKey
WHRGYNQUJQBPER-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):
    3.1
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    76.1
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-(3-(5-hexenyloxy)-1,2,5-thiadiazol-4-yl)pyridine 在 sodium tetrahydroborate 作用下, 以 乙醇丙酮 为溶剂, 反应 18.5h, 生成 3-(3-(5-Hexenyloxy)-1,2,5-thiadiazol-4-yl)-1,2,5,6-tetrahydro-1-methylpyridine
    参考文献:
    名称:
    Muscarinic Analgesics with Potent and Selective Effects on the Gastrointestinal Tract:  Potential Application for the Treatment of Irritable Bowel Syndrome
    摘要:
    Irritable bowel syndrome (IBS) is a pathopysiolocal condition characterized by abnormal bowel habits that are frequently accompanied by abdominal pain. Current therapy based on reducing high-amplitude GI contractions with nonselective muscarinic antagonists is limited in efficacy due to typical muscarinic side effects and provides no pain relief. We have previously found potent antinociceptive agents acting through muscarinic receptors. In the present work, new 1,2,5-thiadiazole-based structures with muscarinic activity have been evaluated both for activity as analgesics in the mouse withing assay and for activity in normalizing spontaneous cluster contractions in ferret jejunum as a model of IBS in humans. (5R,6R)-exo-6-[4-[(4,4,4-Trifluorobutyl)thio]-1,2,5-thiadiazol-3-yl]-1-azabicyclo[3.2.1]octane (35, LY316108/NNC11-2192) was found to offer an exceptional profile combining analgesic potency in mouse writhing (ED(50) = 0.1 mg/kg) along with potency for normalization of GI motility (ED(50) = 0.17 mg/kg). This combination of GI and analgesic potency suggests 35 as an excellent candidate for evaluation as a potential treatment of IBS.
    DOI:
    10.1021/jm9602470
  • 作为产物:
    描述:
    参考文献:
    名称:
    Piperidine compounds and their preparation and use
    摘要:
    公开号:
    EP0384288B1
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文献信息

  • Method of treating urinary bladder dysfunctions with
    申请人:——
    公开号:US05565475A1
    公开(公告)日:1996-10-15
    The present invention relates to a novel method for treating a mammal suffering from urinary bladder dysfunctions.
    本发明涉及一种治疗患有尿道膀胱功能障碍的哺乳动物的新方法。
  • Method of treating schizophrenia
    申请人:Novo Nordisk A/S
    公开号:US05750541A1
    公开(公告)日:1998-05-12
    The present invention relates to a novel method for treating a mammal suffering from or susceptible to schizophrenia and schizophreniform diseases by administering thiadiazole or oxadiazole compounds.
    本发明涉及一种通过给予噻二唑或氧二唑化合物治疗患有或易患精神分裂症和分裂形障碍的哺乳动物的新方法。
  • Method of treating gastrointestinal motility disorders
    申请人:Novo Nordisk A/S
    公开号:US05545638A1
    公开(公告)日:1996-08-13
    The present invention relates to a novel method for treating a mammal suffering from gastrointestinal motility disorders.
    本发明涉及一种治疗患有胃肠蠕动障碍的哺乳动物的新方法。
  • [EN] HETEROCYCLIC COMPOUNDS AND THEIR PREPARATION AND USE<br/>[FR] COMPOSES HETEROCYCLIQUES, LEUR PREPARATION ET UTILISATION
    申请人:NOVO NORDISK A/S
    公开号:WO1994020495A1
    公开(公告)日:1994-09-15
    (EN) The present invention relates to therapeutically active azabicyclic compounds of Formula (1), wherein Z1 is oxygen or sulphur; a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease, severe painful conditions and glaucoma.(FR) L'invention concerne des composés azabicycliques thérapeutiquement actifs, un procédé permettant de les préparer et des compositions pharmaceutiques les comprenant. Ces nouveaux composés servent à stimuler la fonction cognitive du prosencéphale et de l'hippocampe des mammifères, dans notamment le traitement de la maladie d'Alzheimer, des états fortement douloureux et du glaucome.
    (中文) 本发明涉及公式(1)的治疗活性的氮杂双环化合物,其中Z1是氧或硫;一种制备它们的方法以及包含这些化合物的制药组合物。这些新化合物可用作哺乳动物前脑和海马的认知功能的刺激剂,特别适用于治疗阿尔茨海默病、严重疼痛症和青光眼。
  • Piperidine compounds and use
    申请人:Novo Nordisk A/S
    公开号:US05264444A1
    公开(公告)日:1993-11-23
    The present invention relates to therapeutically active piperidine compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease, severe painful conditions and glaucoma.
    本发明涉及治疗活性哌啶化合物,其制备方法以及包含该化合物的制药组合物。这些新型化合物可用作哺乳动物前脑和海马的认知功能刺激剂,特别适用于治疗阿尔茨海默病、严重疼痛和青光眼。
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