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2-(4-((nitrooxy)methyl)phenyl)acetic acid | 646510-50-1

中文名称
——
中文别名
——
英文名称
2-(4-((nitrooxy)methyl)phenyl)acetic acid
英文别名
4-[(nitrooxy)methyl]-benzeneacetic acid;2-[4-(Nitrooxymethyl)phenyl]acetic acid
2-(4-((nitrooxy)methyl)phenyl)acetic acid化学式
CAS
646510-50-1
化学式
C9H9NO5
mdl
——
分子量
211.174
InChiKey
XRNQBJIAVZGRFH-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):
    1.6
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    92.4
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    2-(4-((nitrooxy)methyl)phenyl)acetic acid4-氨基-1-苄基哌啶1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 乙腈 为溶剂, 反应 5.33h, 以79%的产率得到4-(2-((1-benzylpiperidin-4-yl)amino)-2-oxoethyl)benzyl nitrate
    参考文献:
    名称:
    Sigma Receptor Ligands Carrying a Nitric Oxide Donor Nitrate Moiety: Synthesis, In Silico, and Biological Evaluation
    摘要:
    We report the development of molecular hybrids in which a nitrate group serving as nitric oxide (NO) donor is covalently joined to sigma receptor ligands to give candidates for double-targeted cancer therapy. The compounds have been evaluated in radioligand binding assay at both sigma receptors and selected compounds tested for NO release. Compounds 9, 15, 18, 19, and 21 were subjected to MTT test. Compound 15 produced a significant reduction of MCF-7 and Caco-2 cellular viability with comparable IC50 as doxorubicin, being also not toxic for fibroblast HFF-1 cells. Compound 15 has shown a sigma(1), receptor antagonist/sigma(2) receptor agonist profile. Two derivatives of compound 15 lacking the nitrate group did not induce a reduction of MCF-7 cellular viability, suggesting a potential synergistic effect between the sigma receptors and the NO-mediated events. Overall, the combination of NO donor and sigma receptors ligands provided compounds with beneficial effects for the treatment of cancer.
    DOI:
    10.1021/acsmedchemlett.9b00661
  • 作为产物:
    描述:
    4-(溴甲基)苯乙酸silver nitrate 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 1.0h, 以67%的产率得到2-(4-((nitrooxy)methyl)phenyl)acetic acid
    参考文献:
    名称:
    Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use related applications
    摘要:
    该发明描述了新型亚硝化非甾体抗炎药(NSAIDs)及其药用盐,以及包含至少一种亚硝化NSAID的新型组合物,以及可选地,至少一种提供、转移或释放一氧化氮、刺激内源性一氧化氮合成、提高内源性内皮源性舒张因子水平或是一氧化氮合酶底物的化合物,和/或至少一种治疗剂。该发明还提供了包含至少一种亚硝化NSAID和至少一种提供、转移或释放一氧化氮、提高内源性内皮源性舒张因子水平、刺激内源性一氧化氮合成或是一氧化氮合酶底物和/或至少一种治疗剂的新型组合物。该发明还提供了包含至少一种亚硝化NSAID,可选地至少一种一氧化氮供体和/或至少一种治疗剂的新型试剂盒。该发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防由非甾体抗炎化合物使用引起的胃肠道、肾脏和/或呼吸道毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的方法。
    公开号:
    US20040024057A1
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文献信息

  • Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use related applications
    申请人:NitroMed, Inc.
    公开号:US20040024057A1
    公开(公告)日:2004-02-05
    The invention describes novel nitrosated nonsteroidal antiinflammatory drugs (NSAIDs) and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one nitrosated NSAID, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one nitrosated NSAID, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders.
    该发明描述了新型亚硝化非甾体抗炎药(NSAIDs)及其药用盐,以及包含至少一种亚硝化NSAID的新型组合物,以及可选地,至少一种提供、转移或释放一氧化氮、刺激内源性一氧化氮合成、提高内源性内皮源性舒张因子水平或是一氧化氮合酶底物的化合物,和/或至少一种治疗剂。该发明还提供了包含至少一种亚硝化NSAID和至少一种提供、转移或释放一氧化氮、提高内源性内皮源性舒张因子水平、刺激内源性一氧化氮合成或是一氧化氮合酶底物和/或至少一种治疗剂的新型组合物。该发明还提供了包含至少一种亚硝化NSAID,可选地至少一种一氧化氮供体和/或至少一种治疗剂的新型试剂盒。该发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防由非甾体抗炎化合物使用引起的胃肠道、肾脏和/或呼吸道毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的方法。
  • Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
    申请人:Earl A. Richard
    公开号:US20050222243A1
    公开(公告)日:2005-10-06
    The invention describes novel nitrosated nonsteroidal antiinflammatory drugs (NSAIDs) and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one nitrosated NSAID, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one nitrosated NSAID, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders.
    本发明描述了新型亚硝基化非甾体抗炎药(NSAIDs)及其药学上可接受的盐,以及包含至少一种亚硝基化NSAID和可选地至少一种化合物的新型组合物,该化合物捐赠、转移或释放一氧化氮,刺激内源性一氧化氮的合成,提高内源性的内皮源性舒张因子水平或是一氧化氮合酶的底物,和/或至少一种治疗剂。本发明还提供了包含至少一种亚硝基化NSAID和至少一种化合物的新型组合物,该化合物捐赠、转移或释放一氧化氮,提高内源性的内皮源性舒张因子水平,刺激内源性一氧化氮的合成或是一氧化氮合酶的底物和/或至少一种治疗剂。本发明还提供了包含至少一种亚硝基化NSAID、可选地至少一种一氧化氮供体和/或至少一种治疗剂的新型试剂盒。本发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防由非甾体抗炎化合物使用引起的胃肠道、肾脏和/或呼吸毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的方法。
  • NITRIC OXIDE DONATING DIURETIC COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:GARVEY David S.
    公开号:US20080255101A1
    公开(公告)日:2008-10-16
    The invention describes novel compositions and kits comprising at least one nitric oxide enhancing diuretic compound, or pharmaceutically acceptable salts thereof, and, optionally, at least one nitric oxide enhancing compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating conditions resulting from excessive water and/or electrolyte retention; (b) treating cardiovascular diseases; (c) treating renovascular diseases; (d) treating diabetes; (e) treating diseases resulting from oxidative stress; (f) treating endothelial dysfunctions; (g) treating diseases caused by endothelial dysfunctions; (h) treating cirrhosis; (j) treating pre-eclampsia; (k) treating osteoporosis; (l) treating nephropathy; (m) treating peripheral vascular diseases; (n) treating portal hypertension; (o) treating central nervous system disorders; (p) treating metabolic syndrome; (q) treating sexual dysfunctions; and (r) hyperlipidemia. The nitric oxide enhancing diuretic compounds comprise at least one nitric oxide enhancing group linked to the diuretic compound through one or more sites such as carbon, oxygen and/or nitrogen via a bond or moiety that cannot be hydrolyzed.
    这项发明描述了新颖的组合物和试剂盒,包括至少一种增强一氧化氮利尿化合物或其药学上可接受的盐,并且可选地,还包括至少一种增强一氧化氮化合物和/或至少一种治疗剂。该发明还提供了以下方法:(a)治疗由过度水和/或电解质潴留引起的疾病;(b)治疗心血管疾病;(c)治疗肾血管疾病;(d)治疗糖尿病;(e)治疗由氧化应激引起的疾病;(f)治疗内皮功能障碍;(g)治疗由内皮功能障碍引起的疾病;(h)治疗肝硬化;(j)治疗先兆子痫;(k)治疗骨质疏松症;(l)治疗肾病;(m)治疗外周血管疾病;(n)治疗门静脉高压;(o)治疗中枢神经系统疾病;(p)治疗代谢综合征;(q)治疗性功能障碍;以及(r)治疗高脂血症。增强一氧化氮利尿化合物包括至少一个增强一氧化氮基团,通过碳、氧和/或氮等一个或多个位点连接到利尿化合物上,通过无法水解的键或基团连接。
  • NITROSATED NONSTEROIDAL ANTIINFLAMMATORY COMPOUNDS, COMPOSITIONS AND METHODS OF USE
    申请人:EARL Richard A.
    公开号:US20100093671A1
    公开(公告)日:2010-04-15
    The invention describes novel nitrosated nonsteroidal antiinflammatory drugs (NSAIDs) and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one nitrosated NSAID, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one nitrosated NSAID, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders.
    该发明描述了新型亚硝酰化非甾体抗炎药(NSAIDs)及其药学上可接受的盐,并且描述了至少包含一种亚硝酰化NSAID和可选的至少一种化合物的新型组合物,该化合物捐赠、转移或释放一氧化氮,刺激内源性一氧化氮的合成,提高内源性内皮源性松弛因子的水平或是一氧化氮合酶的底物,并/或至少包含一种治疗剂。该发明还提供了至少包含一种亚硝酰化NSAID和至少一种化合物的新型组合物,该化合物捐赠、转移或释放一氧化氮,提高内源性内皮源性松弛因子的水平,刺激内源性一氧化氮的合成或是一氧化氮合酶的底物,并/或至少包含一种治疗剂。该发明还提供了至少包含一种亚硝酰化NSAID,可选的至少一种一氧化氮供体和/或至少一种治疗剂的新型试剂盒。该发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防使用非甾体抗炎化合物导致的胃肠道、肾脏和/或呼吸道毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的方法。
  • Nitrosated Nonsteroidal Antiinflammatory Compounds, Compositions and Methods of Use
    申请人:Earl Richard
    公开号:US20110098253A1
    公开(公告)日:2011-04-28
    The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders comprising administration of novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent.
    该发明还提供了治疗炎症、疼痛和发热的方法;治疗胃肠道疾病的方法;促进伤口愈合的方法;治疗和/或预防非甾体类抗炎化合物使用引起的胃肠道、肾脏和/或呼吸道毒性的方法;治疗炎症性疾病状态和/或疾病的方法;以及治疗和/或预防眼科疾病和/或疾病的新组合物的给药方法,该组合物包括至少一种硝化的非甾体类抗炎药,以及可选地至少一种捐赠、转移或释放一氧化氮、提高内皮源性松弛因子内源水平、刺激内源性一氧化氮合成或是一氧化氮合酶底物和/或至少一种治疗剂。
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