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Methyl 5-pyridin-2-ylsulfanylpentanoate | 114050-40-7

中文名称
——
中文别名
——
英文名称
Methyl 5-pyridin-2-ylsulfanylpentanoate
英文别名
——
Methyl 5-pyridin-2-ylsulfanylpentanoate化学式
CAS
114050-40-7
化学式
C11H15NO2S
mdl
——
分子量
225.312
InChiKey
WUJORPPPTDBNOQ-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):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    64.5
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-O-methyl 6-O-(2-sulfanylidenepyridin-1-yl) hexanedioate 以35%的产率得到
    参考文献:
    名称:
    BARTON, DEREK H. R.;BRIDON, DOMINIQUE;FERNANDEZ-PICOT, ISABEL;ZARD, SAMIR+, TETRAHEDRON, 43,(1987) N 12, 2733-2740
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • PYRIDIN-2YL SULFANYL ACID ESTERS AND PROCESS FOR THE PREPARATION THEREOF
    申请人:Sarma Jadab Chandra
    公开号:US20130131350A1
    公开(公告)日:2013-05-23
    The present invention relates to Pyridin-2-yl sulfanyl acid ester compounds having antiinflammatory properties. The present invention particularly relates to novel anti-inflammatory heterocyclic acid esters of Pyridin-2-yl sulfanyl having the structure of general formula 1 which have been screened for their antiinflammatory activity with respect to inhibition of adhesion of neutrophils, isolated from human peripheral blood, onto the surface of human umbilical vein endothelial cells (HU-VEC) as a result of inhibition of the cytokine-stimulated expression of cell adhesion molecule ICAM-1. The compound RS—Z, 3-(Pyridin-2-yl sulfanyl)-propionic acid pentyl ester (structure 1a, R 1 =H, R 2 =H, R 3 =CH2-COOC5H 11 ) was found to be most effective for ICAM-1 and neutrophil adhesion inhibition and was found to effectively alleviate inflammation mediated by excessive leukocyte infiltration leading to inflammatory disorders or like conditions, such as acute lung injury and acute respiratory distress syndrome in mice.
    本发明涉及具有抗炎性能的吡啶-2-基硫醇酸酯化合物。本发明特别涉及吡啶-2-基硫醇的新型抗炎杂环酸酯,其具有通式1的结构,已经针对其抗炎活性进行了筛选,以抑制从人类外周血液中分离出的中性粒细胞粘附到人脐静脉内皮细胞(HU-VEC)表面,结果是通过抑制细胞粘附分子ICAM-1的细胞因子刺激表达来实现。化合物RS—Z,3-(吡啶-2-基硫醇)-丙酸戊酯(结构1a,R1=H,R2=H,R3=CH2-COOC5H11)被发现对ICAM-1和中性粒细胞粘附抑制效果最显著,并且被发现有效缓解由过度白细胞浸润引起的炎症,导致炎症性疾病或类似症状,如小鼠的急性肺损伤和急性呼吸窘迫综合征。
  • [EN] PYRIDIN- 2 - YL SULFANYL ACID ESTERS AND PROCESS FOR THE PREPARATION THEREOF<br/>[FR] ESTERS DE PYRIDIN-2-YLSULFANYLACIDES ET LEUR PROCÉDÉ DE SYNTHÈSE
    申请人:COUNCIL SCIENT IND RES
    公开号:WO2012011123A1
    公开(公告)日:2012-01-26
    The present invention relates to Pyridin-2-yl sulfanyl acid ester compounds having antiinflammatory properties. The present invention particularly relates to novel anti-inflammatory heterocyclic acid esters of Pyridin-2-yl sulfanyl having the structure of general formula 1 which have been screened for their antiinflammatory activity with respect to inhibition of adhesion of neutrophils, isolated from human peripheral blood, onto the surface of human umbilical vein endothelial cells (HUVEC) as a result of inhibition of the cytokine-stimulated expression of cell adhesion molecule ICAM-1. The compound RS-Z, 3-(Pyridin-2-yl sulfanyl)-propionic acid pentyl ester (structure la, R1 = H, R2 = H, R3 = CH2COOC5H11) was found to be most effective for ICAM-1 and neutrophil adhesion inhibition and was found to effectively alleviate inflammation mediated by excessive leukocyte infiltration leading to inflammatory disorders or like conditions, such as acute lung injury and acute respiratory distress syndrome in mice.
    本发明涉及具有抗炎性质的吡啶-2-基巯酸酯化合物。本发明特别涉及一类新型的抗炎杂环酸酯,其具有通用公式1的结构,并且已经通过抑制从人外周血中分离的中性粒细胞粘附到人脐静脉内皮细胞(HUVEC)表面的能力来筛选其抗炎活性,这是通过抑制细胞粘附分子ICAM-1的细胞因子刺激表达的结果。发现化合物RS-Z,3-(吡啶-2-基巯基)-丙酸戊酯(结构la,R1 = H,R2 = H,R3 = CH2COOC5H11)对ICAM-1和中性粒细胞粘附抑制最有效,并且发现它有效地缓解了由过度白细胞浸润导致的炎症介导的炎症疾病或类似状况,例如小鼠的急性肺损伤和急性呼吸窘迫综合征。
  • The invention of radical reactions
    作者:Derek H.R. Barton、Dominique Bridon、Isabel Fernandaz-Picot、Samir Z. Zard
    DOI:10.1016/s0040-4020(01)86878-2
    日期:1987.1
    Esters (mixed anhydrides) derived from aliphatic or alicyclic carboxylic acids (RCO2H) and thiohydroxamic acids or undergo a thermally or photochemically induced radical chain reaction to give sulphides with loss of carbon dioxide. On irradiation at low-temperature however, the chain reaction is essentially supressed. Under these conditions moderate to good yields of dimers R-R are obtained from primary
    衍生自脂肪族或脂环族羧酸(RCO 2 H)和硫代异羟肟酸的酯(混合酸酐),或经过热或光化学诱导的自由基链反应,生成硫化物,并减少二氧化碳的损失。然而,在低温下照射时,链反应基本上被抑制。在这些条件下,从伯酸获得中等至良好产率的二聚体RR。讨论了这些观察结果的机理和综合意义。
  • BARTON, DEREK H. R.;BRIDON, DOMINIQUE;FERNANDEZ-PICOT, ISABEL;ZARD, SAMIR+, TETRAHEDRON, 43,(1987) N 12, 2733-2740
    作者:BARTON, DEREK H. R.、BRIDON, DOMINIQUE、FERNANDEZ-PICOT, ISABEL、ZARD, SAMIR+
    DOI:——
    日期:——
  • PYRIDIN-2-YL SULFANYL ACID ESTERS AND PROCESS FOR THE PREPARATION THEREOF
    申请人:Council of Scientific & Industrial Research
    公开号:EP2595957B1
    公开(公告)日:2014-08-13
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