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4-(4-morpholinyl)butanethiol | 778604-03-8

中文名称
——
中文别名
——
英文名称
4-(4-morpholinyl)butanethiol
英文别名
4-(Morpholin-4-yl)butane-1-thiol;4-morpholin-4-ylbutane-1-thiol
4-(4-morpholinyl)butanethiol化学式
CAS
778604-03-8
化学式
C8H17NOS
mdl
——
分子量
175.295
InChiKey
KMDMNFSGDOSEGU-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:
    11
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    13.5
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE AND PHARMACEUTICALS CONTAINING THE SAME
    申请人:CHUGAI SEIYAKU KABUSHIKI KAISHA
    公开号:US20160002251A1
    公开(公告)日:2016-01-07
    The present invention provides a dihydropyridazine-3,5-dione derivative or a salt thereof, or a solvate of the compound or the salt, a pharmaceutical drug, a pharmaceutical composition, a sodium-dependent phosphate transporter inhibitor, and a preventive and/or therapeutic agent for hyperphosphatemia, secondary hyperparathyroidism, chronic renal failure, chronic kidney disease, and arteriosclerosis associated with vascular calcification comprising the compound as an active ingredient, and a method for prevention and/or treatment.
    本发明提供了一种二氢吡啶嗪-3,5-二酮衍生物或其盐,或化合物或盐的溶剂化合物,一种药物,一种药物组合物,一种依赖性磷酸盐转运体抑制剂,以及作为活性成分的化合物的高血症、继发性甲状旁腺功能亢进症、慢性肾功能衰竭、慢性肾病和与血管化相关的动脉硬化的预防和/或治疗剂,以及预防和/或治疗的方法。
  • Fused bicyclic amide compounds and medicinal use thereof
    申请人:——
    公开号:US20030203909A1
    公开(公告)日:2003-10-30
    The present invention provides a compound represented by the formula (I) 1 wherein ring A is benzene, cyclohexane, pyridine, piperidine or a derivative thereof, imidazole or a derivative thereof and the like, ring B is benzene, cyclohexane, pyrrole or a derivative thereof, furan, thiophene and the like, R 1 , R 2 and R 3 are each hydrogen, alkyl, halogen, hydroxyl group, alkoxy and the like, W is hydrogen, alkyl or hydroxycarbonylalkyl, X is halogen, cyano, nitro and the like, X′ is hydrogen, halogen and the like, and Y is alkyl, hydroxyalkyl, hydroxycarbonylalkyl, aminoalkyl and the like, a salt thereof, and a pharmaceutical agent containing the compound. The compound of the present invention shows a superior inhibitory effect on the proliferation of activated lymphocyte and is useful as an agent for the prophylaxis or treatment of various autoimmune diseases.
    本发明提供了一种由以下化学式(I)1所代表的化合物,其中环A为苯、环己烷吡啶哌啶或其衍生物咪唑或其衍生物等,环B为苯、环己烷吡咯或其衍生物呋喃噻吩等,R1、R2和R3分别为氢、烷基、卤素、羟基、烷氧基等,W为氢、烷基或羟基羰基烷基,X为卤素、基、硝基等,X′为氢、卤素等,Y为烷基、羟基烷基、羟基羰基烷基、基烷基等,其盐和含有该化合物的药物。本发明的化合物对活化淋巴细胞的增殖具有优越的抑制作用,并可用作各种自身免疫性疾病的预防或治疗剂。
  • Omega-quaternary ammonium alkyl esters and thioesters of acidic nonsteroidal antiinflammatory drugs
    申请人:SYNTEX PHARMACEUTICALS INTERNATIONAL LIMITED
    公开号:EP0289262A2
    公开(公告)日:1988-11-02
    Quaternary ammonium alkyl esters and thioesters of acidic nonsteroidal anti-inflammatory drugs (NSAIDs) are disclosed. These esters and thioesters display the anti-­inflammatory profile of the parent NSAIDs with greatly reduced gastrointestinal irritancy, providing a more favorable separation of therapeutic activity and toxicological side effects than the parent NSAIDs.
    本发明公开了酸性非甾体抗炎药(NSAIDs)的季烷基酯和代酯。这些酯类酯类具有母体非甾体抗炎药的抗炎特性,但胃肠道刺激性大大降低,与母体非甾体抗炎药相比,能更有效地将治疗活性和毒副作用分开。
  • FUSED BICYCLIC AMIDE COMPOUNDS AND MEDICINAL USE THEREOF
    申请人:Mitsubishi Pharma Corporation
    公开号:EP1310488A1
    公开(公告)日:2003-05-14
    The present invention provides a compound represented by the formula (I) wherein ring A is benzene, cyclohexane, pyridine, piperidine or a derivative thereof, imidazole or a derivative thereof and the like, ring B is benzene, cyclohexane, pyrrole or a derivative thereof, furan, thiophene and the like, R1, R2 and R3 are each hydrogen, alkyl, halogen, hydroxyl group, alkoxy and the like, W is hydrogen, alkyl or hydroxycarbonylalkyl, X is halogen, cyano, nitro and the like, X' is hydrogen, halogen and the like, and Y is alkyl, hydroxyalkyl, hydroxycarbonylalkyl, aminoalkyl and the like, a salt thereof, and a pharmaceutical agent containing the compound. The compound of the present invention shows a superior inhibitory effect on the proliferation of activated lymphocyte and is useful as an agent for the prophylaxis or treatment of various autoimmune diseases.
    本发明提供了一种由式(I)表示的化合物 其中环 A 是苯、环己烷吡啶哌啶或其衍生物咪唑或其衍生物等,环 B 是苯、环己烷吡咯或其衍生物呋喃噻吩等,R1、R2 和 R3 分别是氢、烷基、卤素、羟基、烷氧基等,W 是氢、烷基或羟基羰基烷基,X 是卤素、基、硝基等、W为氢、烷基或羟基羰基烷基,X为卤素、基、硝基等,X'为氢、卤素等,Y为烷基、羟基烷基、羟基羰基烷基、基烷基等,其盐以及含有该化合物的药剂。本发明的化合物对活化淋巴细胞的增殖有很好的抑制作用,可作为预防或治疗各种自身免疫性疾病的药物。
  • DIHYDROPYRIDAZINE-3,5-DIONE DERIVATIVE
    申请人:Chugai Seiyaku Kabushiki Kaisha
    公开号:EP2975030A1
    公开(公告)日:2016-01-20
    The present invention provides a dihydropyridazine-3,5-dione derivative or a salt thereof, or a solvate of the compound or the salt, a pharmaceutical drug, a pharmaceutical composition, a sodium-dependent phosphate transporter inhibitor, and a preventive and/or therapeutic agent for hyperphosphatemia, secondary hyperparathyroidism, and chronic renal failure, comprising the compound as an active ingredient, and a method for prevention and/or treatment.
    本发明提供了一种二氢哒嗪-3,5-二酮衍生物或其盐,或该化合物或该盐的溶液剂、一种药物、一种药物组合物、一种依赖性磷酸盐转运体抑制剂,以及一种预防和/或治疗高血症、继发性甲状旁腺功能亢进症和慢性肾功能衰竭的药物,其中包含该化合物作为活性成分,以及一种预防和/或治疗方法。
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