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1-戊氧基苯并三唑 | 60455-00-7

中文名称
1-戊氧基苯并三唑
中文别名
——
英文名称
1-pentyloxy-1H-benzo[d]-1,2,3-triazole
英文别名
1-pentyloxy-1H-benzotriazole;1-Pentoxybenzotriazole
1-戊氧基苯并三唑化学式
CAS
60455-00-7
化学式
C11H15N3O
mdl
——
分子量
205.26
InChiKey
AXZTWHHHIRFDOQ-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    39.9
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:ed317753a2f2eb7fb3cf4c5ff0d47ded
查看

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:
    描述:
    1-溴戊烷1-羟基苯并三唑potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 0.5h, 以93.4%的产率得到1-戊氧基苯并三唑
    参考文献:
    名称:
    Design, Synthesis and Antidepressant and Anticonvulsant Effect of 1-Alkoxy-1H-Benzo[d]-1,2,3-Triazole Derivatives
    摘要:
    背景:设计、制备并评估了21种新型1-烷氧基-1H-苯并[d]-1,2,3-噻唑化合物在小鼠中的抗抑郁和抗惊厥效果。 方法:化合物19在强迫游泳试验(FST)中显著减少了动物的失动时间,而不改变开放场实验中的运动活动,其疗效高于参照标准药物氟西汀。化合物19显著提高了小鼠大脑中5-HT、NE和5-HIAA的水平,这表明其抗抑郁活性可能与这些神经递质有关。在癫痫测试中,化合物19在对抗MES方面也表现出更好的抗惊厥活性,同时没有显示出神经毒性(300 mg/kg)。 结论:我们的数据表明,化合物19可能作为抗抑郁药用于癫痫患者。
    DOI:
    10.2174/1570180813666160826113018
点击查看最新优质反应信息

文献信息

  • Synthesis and Evaluation of 1-hydroxybenzotriazole Derivatives: Dual Inhibitors of Carbonic Anhydrase II and Sodium Hydrogen Exchanger I
    作者:Dhandeep Singh、Nirmal Singh
    DOI:10.2174/1570178617999201014164710
    日期:2021.7.29
    <p>Ischemia reperfusion injury is responsible for impaired graft functioning in organ transplants, cerebral dysfunction, ischemic heart diseases, systemic inflammatory response syndrome, gastrointestinal dysfunction, and multiple organ dysfunction syndromes. Intracellular pH is critical for cell survival in ischemia reperfusion injury. Sodium hydrogen exchanger I and carbonic anhydrase II are critical in the regulation of intracellular pH. Inhibition of sodium hydrogen exchanger I and carbonic anhydrase II during reperfusion is found to ameliorate ischemia reperfusion injury separately. An attempt is made to synthesize dual inhibitors of sodium hydrogen exchanger and carbonic anhydrase to have better potential drug molecule in ischemia reperfusion injury treatment. The hydroxybenzotriazole is considered as a central pharmacophore for this dual activity and 12 derivatives are synthesized. All derivatives are tested for sodium hydrogen exchanger I and carbonic anhydrase II inhibitory activity. The tosylate derivative (12) is found to be the most potent derivative with IC50 158.7± 8.4 μM for carbonic anhydrase II and 31.07 ± 1.06 μM for sodium hydrogen exchanger I. Although the potency is less than standard drugs but this is the first report of dual inhibitor of carbonic anhydrase II and sodium hydrogen exchanger.</p> </sec></div> <div class="value-text ch">缺血再灌注损伤是器官移植中移植物功能受损的原因,也与脑功能障碍、缺血性心脏病、全身炎症反应综合征、胃肠功能障碍和多器官功能障碍综合征有关。细胞内pH对于缺血再灌注损伤中的细胞存活至关重要。<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白I和<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶II在调节细胞内pH方面起着关键作用。在再灌注期间抑制<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白I和<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶II分别被发现可以缓解缺血再灌注损伤。为了在缺血再灌注损伤治疗中获得更好的潜在药物分子,尝试合成<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白和<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶的双重<a href=https://www.molaid.com/fenzi/4221 target="_blank">抑制剂</a>。<a href=https://www.molaid.com/MS_17524 target="_blank">羟基苯并三唑</a>被认为是这种双重活性的中心药效团,合成了12种衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>。所有衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>均经过测试,用于检测<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白I和<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶II的抑制活性。对<a href=https://www.molaid.com/MS_24915 target="_blank">甲磺酸</a>酯衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>(12)发现是最有效的衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>,对<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶II的IC50为158.7±8.4 μM,对<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白I的IC50为31.07±1.06 μM。尽管其效力低于标准药物,但这是对<a href=https://www.molaid.com/MS_20299 target="_blank">碳酸</a>酐酶II和<a href=https://www.molaid.com/MS_5237 target="_blank">钠</a>氢交换蛋白的双重<a href=https://www.molaid.com/fenzi/4221 target="_blank">抑制剂</a>的首次报道。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Preparation and Use of Isolactosamine and Intermediates therefor</div> <div class="value"> <div class="value-text"> <span>申请人:</span>Glycom A/S </div> <div class="value-text"> <span>公开号:</span>US20140303363A1 </div> <div class="value-text"> <span>公开(公告)日:</span>2014-10-09 </div> <div class="value-text en">The invention relates to providing isolactosamine (Galβ1-3GlcNH 2 , formula 1) and salts thereof in the form of either anomer or mixture thereof, as well as hydrates or solvates of the free base and salts thereof. The synthesis of isolactosamine and its use in the synthesis of lacto-N-biose containing oligosaccharides are also disclosed.</div> <div class="value-text ch">本发明涉及提供Galβ1-3GlcNH2(式1)及其盐的异构体或混合物的形式,以及自由碱和其盐的<a href=https://www.molaid.com/MS_34644 target="_blank">水</a>合物或溶剂合物。本发明还公开了Galβ1-3GlcNH2的合成以及其在合成含有<a href=https://www.molaid.com/MS_71840 target="_blank">乳糖</a>N-<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>糖的<a href=https://www.molaid.com/fenzi/4667 target="_blank">寡糖</a>中的应用。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">[EN] PREPARATION AND USE OF ISOLACTOSAMINE AND INTERMEDIATES THEREFOR<br/>[FR] PRÉPARATION ET UTILISATION D'ISOLACTOSAMINE ET INTERMÉDIAIRES S'Y RAPPORTANT</div> <div class="value"> <div class="value-text"> <span>申请人:</span>GLYCOM AS </div> <div class="value-text"> <span>公开号:</span>WO2013083136A1 </div> <div class="value-text"> <span>公开(公告)日:</span>2013-06-13 </div> <div class="value-text en">The invention relates to providing isolactosamine (Galβ1-3GlcN2, formula 1) and salts thereof in the form of either anomer or mixture thereof, as well as hydrates or solvates of the free base and salts thereof. Isolactosamine derivatives of formula 2, the synthesis of isolactosamine by hydrogenolysis of said derivatives and the use of isolactosamine in the synthesis of lacto-N-biose containing oligosaccharides, through the steps of masking the amino group of isolactosamine with a suitable protecting group, protecting the OH-groups, activating the anomeric position to obtain a lacto-N-biosyl donor and coupling the lacto-N-biosyl donor to a desired sugar moiety, are also disclosed.</div> <div class="value-text ch">本发明涉及以α或β异构体或其混合形式的盐的形式提供Galβ1-3GlcN2(式1)和其<a href=https://www.molaid.com/MS_34644 target="_blank">水</a>合物或溶剂化物,以及式2的Isolactosamine衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>,通过遮盖适当的保护基来保护Isolactosamine的<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>基团,保护OH基团,激活异构位置以获得lacto-N-<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>糖供体,并将lacto-N-<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>糖供体与所需的糖基团偶联,用于合成含有lacto-N-biose的<a href=https://www.molaid.com/fenzi/4667 target="_blank">寡糖</a>。同时还公开了通过上述衍<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>的氢解来合成Isolactosamine的方法。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Electrochemically degradable polymers</div> <div class="value"> <div class="value-text"> <span>申请人:</span>d'Alarcao Marc </div> <div class="value-text"> <span>公开号:</span>US20090024074A1 </div> <div class="value-text"> <span>公开(公告)日:</span>2009-01-22 </div> <div class="value-text en">The present invention discloses polymeric materials that incorporate a modified quinone moiety, either to cross-link the polymer or as a monomeric unit of the polymer These polymeric materials can be efficiently degraded through electrochemical reduction of the quinone leading to rapid hydrolysis of the pendant chemical groups and degradation of the polymer. Quinone-containing compositions and methods of producing electrochemically degradable polymers are disclosed. The methods and compositions of the present invention can be used in a wide variety of applications, including, but not limited to, drug delivery, tissue regeneration, biomedical implants, and electronic systems.</div> <div class="value-text ch">本发明揭示了聚合材料,其中包括经过修饰的醌基团,可以用于交联聚合物或作为聚合物的单体单元。这些聚合材料可以通过醌的电<a href=https://www.molaid.com/fenzi/4464 target="_blank">化学</a>还原有效地降解,导致悬挂<a href=https://www.molaid.com/fenzi/4464 target="_blank">化学</a>基团的快速<a href=https://www.molaid.com/MS_34644 target="_blank">水</a>解和聚合物的降解。本发明揭示了含醌的组合物和制备电<a href=https://www.molaid.com/fenzi/4464 target="_blank">化学</a>可降解聚合物的方法。本发明的方法和组合物可以用于各种应用,包括但不限于药物传递、组织再生、<a href=https://www.molaid.com/fenzi/4147 target="_blank">生物</a>医学植入物和电子系统。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Azacyclyl (thio) ureidoacetyl-Verbindungen und Verfahren zu ihrer Herstellung</div> <div class="value"> <div class="value-text"> <span>申请人:</span>CIBA-GEIGY AG </div> <div class="value-text"> <span>公开号:</span>EP0015240A1 </div> <div class="value-text"> <span>公开(公告)日:</span>1980-09-03 </div> <div class="value-text en"> Die Erfindung betrifft Azacyctyl(thio)-ureiodoacetamido- cephem- Verbindungen der Formel worin R1 Wasserstoff, Halogen, veräthertes Hydroxy oder Mercapto, oder einen Rest -CH2-C(=O)-R6, worin R6 Wasserstoff, Hydroxy, Niederalkoxy, Niederalkyl oder gegebenenfalls substituiertes Amino darstellt, R2 Hydroxy oder eine verätherte Hydroxygruppe, die, zusammen mit der Gruppe -C=0, eine unter physiologischen Bedingungen spaltbare veresterte Carboxylgruppe -C(=O)-OR5 bildet, R3 Wasserstoff, einen gegebenenfalls substituierten, ungesättigten cyclischen Kohlenwasserstoffrest oder Heterocyclyl, X Sauerstoff oder Schwefel, der Index n den Wert 1 oder 2, R. Wasserstoff, einen gegebenenfalls substituierten niederaliphatischen oder cycloaliphatischen Rest oder Acyl und Y ein die Stickstoffatome durch zwei Kohlenstoffatome trennendes Niederalkylen bedeuten, Salze von salzbildenden Verbindungen der Formel I, sowie lsomere davon, sowie Verfahren zu ihrer Herstellung, solche Stoffe der Formel 1 enthaltende Präparate und deren Verwendung sowie entsprechende neue Zwischenprodukte. Die Herstellung dieser Verbindungen erfolgt in an sich bekannte Weise, z.B. durch Einführen der Acylgruppe in eine entsprechende 7ß-Amino-3-cephem-Verbindung. Die Verbindungen haben antibiotische Wirksamkeit und können zur Bekämpfung von Infektionen verwendet werden. </div> <div class="value-text ch">本发明涉及式如下的氮杂辛基(<a href=https://www.molaid.com/MS_22128 target="_blank">硫</a>代)-<a href=https://www.molaid.com/fenzi/4421 target="_blank">脲</a><a href=https://www.molaid.com/MS_20835 target="_blank">碘</a>乙酰胺-头孢化合物 其中 R1 是氢、卤素、醚化羟基或巯基,或自由基 -<a href=https://www.molaid.com/MS_1215156 target="_blank">CH2</a>-C(=O)-R6,其中 R6 是氢、羟基、低级烷氧基、低级烷基或任选取代的<a href=https://www.molaid.com/MS_37224 target="_blank">氨</a>基,R2 是羟基或醚化羟基,该羟基与基团 -C=0、R3 是氢、任选取代的不饱和<a href=https://www.molaid.com/fenzi/4519 target="_blank">环烃</a>基或杂<a href=https://www.molaid.com/fenzi/4519 target="_blank">环烃</a>基,X 是氧或<a href=https://www.molaid.com/MS_22128 target="_blank">硫</a>,指数 n 的值为 1 或 2,R.氢、任选取代的低级脂肪族或环脂族自由基或酰基,Y 是将氮原子隔开两个碳原子的低级亚烷基、式 I 的成盐化合物的盐及其异构体、其制备工艺、含有式 1 的此类物质的制剂及其用途以及相应的新中间体。 这些化合物的制备方法本身是已知的,例如将酰基引入相应的 7ß-amino-3-cephem 化合物中。 这些化合物具有抗生素活性,可用于抗感染。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101a17y966331fc49M0&inchikey=AXZTWHHHIRFDOQ-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_2906" class="compound-item" title="阿立必利">阿立必利</a> <a target="_blank" href="https://www.molaid.com/MS_23149294" class="compound-item" title="试剂4,7-Bis(5-bromo-2-thienyl)-5,6-difluoro-2-(2-hexyldecyl)-2H-benzotriazole">试剂4,7-Bis(5-bromo-2-thienyl)-5,6-difluoro-2-(2-hexyldecyl)-2H-benzotriazole</a> <a target="_blank" href="https://www.molaid.com/MS_12235" class="compound-item" title="苯并三氮唑-N,N,N',N'-四甲基脲六氟磷酸盐">苯并三氮唑-N,N,N',N'-四甲基脲六氟磷酸盐</a> <a target="_blank" href="https://www.molaid.com/MS_12236" class="compound-item" title="苯并三氮唑-5-甲酸乙酯">苯并三氮唑-5-甲酸乙酯</a> <a target="_blank" 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