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(S)-2-allylamino-4-methylsulfanylbutyric acid

中文名称
——
中文别名
——
英文名称
(S)-2-allylamino-4-methylsulfanylbutyric acid
英文别名
AMSB;(2S)-4-methylsulfanyl-2-(prop-2-enylamino)butanoic acid
(S)-2-allylamino-4-methylsulfanylbutyric acid化学式
CAS
——
化学式
C8H15NO2S
mdl
——
分子量
189.279
InChiKey
ICHPRNNVJZNMNM-ZETCQYMHSA-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):
    -1.2
  • 重原子数:
    12
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

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

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文献信息

  • Organic salts and their use as reagents in electrochemical reactions
    申请人:Callens Roland
    公开号:US20060049061A1
    公开(公告)日:2006-03-09
    Use of an organic compound salt of general formula A-XY   (I) wherein A means an organic residue, X means a charged group and Y means a counter-ion, as a reagent in an electrochemical reaction and organic compound salt corresponding to the formula R1R2ZC-T-Q-XY wherein X is a charged group, Y is a counter-ion, Z is a group capable of being substituted, R1 and R2 mean organic residues, T means a group containing a hetero atom selected among N-R4, O and S, and Q means a connecting group linking the hetero atom and the charged group.
    使用通式A-XY的有机化合物盐,其中A表示有机残基,X表示带电团,Y表示反离子,在电化学反应中作为试剂,以及符合以下公式的有机化合物盐R1R2ZC-T-Q-XY,其中X为带电团,Y为反离子,Z为可被取代的基团,R1和R2表示有机残基,T表示包含在N-R4,O和S中选择的杂原子的基团,Q表示连接杂原子和带电团的连接基团。
  • Synthesis, molecular modeling and biological evaluation of novel 2-allyl amino 4-methyl sulfanyl butyric acid as α-amylase and α-glucosidase inhibitor
    作者:Kannan Balan、Perumal Perumal、Narayanan Sundarabaalaji、Thayumanavan Palvannan
    DOI:10.1016/j.molstruc.2014.09.086
    日期:2015.2
    In the present study 2-allyl amino 4-methyl sulfanyl butyric acid (AMSB) was synthesized in good yield. AMSB was characterized by Fourier transforms infrared spectroscopy (FTIR), Nuclear magnetic resonance (NMR) (H-1 and C-13) and Liquid chromatography mass spectrometry (LCMS). The radical scavenging activity and reducing power assay of AMSB was assessed using 1-1-diphenyl 2-picryl hydrazyl (DPPH), 2,2'-azino-bis (3-ethyl benzothiazoline-6-sulfonic acid) (ABTS) and ferric ion reducing antioxidant power assay (FRAP) and was found to be 44.1, 34.71 and 41.7 mu g/ml respectively. The compound showed effective inhibition against alpha-amylase and alpha-glucosidase. AMSB was identified to be a reversible mixed noncompetitive inhibitor of alpha-amylase and alpha-glucosidase. The molecular docking study was carried out to evaluate the specific groove binding properties and affords valuable information of AMSB binding mode in the active site of alpha-glucosidase the study may lead to the which leads to the rational design of new class of antidiabetic drugs targeting alpha-glucosidase based on AMSB in near future. (C) 2014 Elsevier B.V. All rights reserved.
  • ORGANIC SALTS AND THEIR USE AS REAGENTS IN ELECTROCHEMICAL REACTIONS
    申请人:Solvay SA
    公开号:EP1540037A1
    公开(公告)日:2005-06-15
  • US7767073B2
    申请人:——
    公开号:US7767073B2
    公开(公告)日:2010-08-03
  • [EN] ORGANIC SALTS AND THEIR USE AS REAGENTS IN ELECTROCHEMICAL REACTIONS<br/>[FR] SELS ORGANIQUES ET LEUR UTILISATION EN TANT QUE REACTIFS DANS DES REACTIONS ELECTROCHIMIQUES
    申请人:SOLVAY
    公开号:WO2004024991A1
    公开(公告)日:2004-03-25
    Use of an organic compound salt of general formula (I) : A-X Y wherein A means an organic residue, X means a charged group and Y means a counter-ion, as a reagent in an electrochemical reaction and organic compound salt corresponding to the formula R1R2ZC-T-Q-X Y wherein X is a charged group, Y is a counter-ion, Z is a group capable of being substituted, R1 and R2 mean organic residues, T means a group containing a hetero atom selected among N-R4, O and S, and Q means a connecting group linking the hetero atom and the charged group.
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