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(R)-4-(nitrooxy)butyl 2-((5-(1,2-dithiolan-3-yl)pentanoyl)oxy)benzoate | 1357392-70-1

中文名称
——
中文别名
——
英文名称
(R)-4-(nitrooxy)butyl 2-((5-(1,2-dithiolan-3-yl)pentanoyl)oxy)benzoate
英文别名
4-nitrooxybutyl 2-[5-[(3R)-dithiolan-3-yl]pentanoyloxy]benzoate
(R)-4-(nitrooxy)butyl 2-((5-(1,2-dithiolan-3-yl)pentanoyl)oxy)benzoate化学式
CAS
1357392-70-1
化学式
C19H25NO7S2
mdl
——
分子量
443.542
InChiKey
RONOJSOBVVSEJP-OAHLLOKOSA-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):
    4.4
  • 重原子数:
    29
  • 可旋转键数:
    14
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    158
  • 氢给体数:
    0
  • 氢受体数:
    9

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

  • 作为产物:
    参考文献:
    名称:
    NOSH-Aspirin: A Novel Nitric Oxide–Hydrogen Sulfide-Releasing Hybrid: A New Class of Anti-inflammatory Pharmaceuticals
    摘要:
    A series of new hybrids of aspirin (ASA), bearing both nitric oxide (NO) and hydrogen sulfide (H2S)-releasing moieties were synthesized and designated as NOSH compounds (1-4). NOSH-1 (4-(3-thioxo-3H-1,2-dithiol-5-yl) phenyl 24(4-(nitrooxy)butanoyl)oxy) benzoate); NOSH-2 (4-(nitrooxy)butyl (2-((4-(3-thioxo-3H-1,2-dithiol-5-yl)phenoxy)carbonyl)phenyl)); NOSH-3 (4-carbamothioylphenyl 2-((4-(nitrooxy)butanoyl)oxy)benzoate); and NOSH-4 (4-(nitrooxy)butyl 2-(5-((R)-1,2-dithiolan-3-yl)pentanoyloxy)benzoate). The cell growth inhibitory properties of compounds 1-4 were evaluated in eleven different human cancer cell lines of six different tissue origins. These cell lines are of adenomatous (colon, pancreatic, lung, prostate), epithelial (breast), and lymphocytic (leukemia) origin. All NOSH compounds were extremely effective in inhibiting the growth of these cell lines. NOSH-1 was the most potent, with an IC50 of 48 +/- 3 nM in HT-29 colon cancer cells. This is the first NSAID-based compound with such potency. This compound was also devoid of any cellular toxicity, as determined by LDH release. NOSH-1 was comparable to aspirin in its anti-inflammatory properties, using the carrageenan rat paw edema model.
    DOI:
    10.1021/ml300002m
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文献信息

  • NO- and H2S-releasing compounds
    申请人:RESEARCH FOUNDATION OF THE CITY UNIVERSITY OF NEW YORK
    公开号:US10450260B2
    公开(公告)日:2019-10-22
    This disclosure relates to compounds containing both an NO-releasing moiety and an H2S-releasing moiety and the use of such compounds in treating inflammatory diseases, including cancers.
    本公开涉及同时含有释放 NO 的分子和释放 H2S 的分子的化合物,以及此类化合物在治疗炎症性疾病(包括癌症)中的应用。
  • NO- AND H2S- RELEASING COMPOUNDS
    申请人:Research Foundation Of The City University Of New York
    公开号:EP2744487B1
    公开(公告)日:2016-10-05
  • [EN] NO- AND H2S- RELEASING COMPOUNDS<br/>[FR] COMPOSÉS LIBÉRANT NO ET H2S
    申请人:UNIV CITY NEW YORK RES FOUND
    公开号:WO2013025790A3
    公开(公告)日:2013-05-10
  • Method of Priming Plants Against Abiotic Stress Factors
    申请人:Research Foundation of the City University of New York
    公开号:US20170174651A1
    公开(公告)日:2017-06-22
    A method of reducing cellular damage to a plant by treating the plant with a compound containing an NO-releasing moiety and an H 2 S-releasing moiety covalently bonded to an aspirin derived core or a NOSH compound is claimed. The compounds may also be used in a method of priming a plant against abiotic stress factors and a method of promoting plant growth.
  • US9688607B2
    申请人:——
    公开号:US9688607B2
    公开(公告)日:2017-06-27
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同类化合物

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