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3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine | 118795-59-8

中文名称
——
中文别名
——
英文名称
3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine
英文别名
4,4'-(1,2,4,5-tetrazine-3,6-diyl)diphenol;Phenol, 4,4'-(1,2,4,5-tetrazine-3,6-diyl)bis-;4-[6-(4-hydroxyphenyl)-1,2,4,5-tetrazin-3-yl]phenol
3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine化学式
CAS
118795-59-8
化学式
C14H10N4O2
mdl
——
分子量
266.259
InChiKey
CPOMHYIJGJUENL-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):
    1.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    92
  • 氢给体数:
    2
  • 氢受体数:
    6

上下游信息

  • 下游产品
    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:
    3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine 在 3Fe(2+)*3HO(1-)*1.5C4O4(2-) 作用下, 以 乙腈 为溶剂, 反应 20.0h, 以53%的产率得到2,5-双(4-羟基苯基)-1,3,4-噁二唑
    参考文献:
    名称:
    Study of Heterogeneous Catalysis by Iron-Squarate based 3D Metal Organic Framework for the Transformation of Tetrazines to Oxadiazole derivatives
    摘要:
    We present here a simple, milder, and environmentally benign heterogeneous catalytic method for the transformation of tetrazines to oxadiazole derivatives at room temperature (25 degrees C) using our earlier synthesized iron-squarate based 3D metal organic framework, [Fe-3(OH)(3)(C4O4)(C4O4)(0.5)](n) (FeSq-MOF).
    DOI:
    10.1021/ic5003258
  • 作为产物:
    描述:
    4-羟基苯甲腈溶剂黄146 、 sodium nitrite 作用下, 生成 3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine
    参考文献:
    名称:
    3,6-Substituted-1,2,4,5-tetrazines: tuning reaction rates for staged labeling applications
    摘要:
    涉及四氮杂环的环加成反应已被证明是多种应用的强大生物正交工具。可以想象,通过调整反应速率,可以实现基于四氮杂环的顺序和选择性标记。通过改变四氮杂环上的取代基,已实现与相同的二烯亲和体相比超过200倍的环加成速率变化。与不同的二烯亲和体(如诺尔本烯)耦合时,反应速率差异可超过14,000倍。这些取代的四氮杂环在不同条件下的选择性标记中非常有用。
    DOI:
    10.1039/c4ob00280f
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文献信息

  • BIO-ORTHOGONAL DRUG ACTIVATION
    申请人:KONINKLIJKE PHILIPS N.V.
    公开号:US20160106859A1
    公开(公告)日:2016-04-21
    The invention relates to a Prodrug activation method, for therapeutics, wherein use is made of abiotic reactive chemical groups that exhibit bio-orthogonal reactivity towards each other. The invention also relates to a Prodrug kit comprising at least one Prodrug and at least one Activator, wherein the Prodrug comprises a Drug and a first Bio-orthogonal Reactive Group (the Trigger), and wherein the Activator comprises a second Bio-orthogonal Reactive Group. The invention also relates to targeted therapeutics used in the above-mentioned method and kit. The invention particularly pertains to antibody-drug conjugates and to bi- and trispecific antibody derivatives.
    该发明涉及一种用于治疗学的原药激活方法,其中使用了表现出彼此生物正交反应性的非生物活性化学基团。该发明还涉及一种包含至少一种原药和至少一种激活剂的试剂盒,其中原药包含药物和第一个生物正交反应基团(触发器),而激活剂包含第二个生物正交反应基团。该发明还涉及在上述方法和试剂盒中使用的靶向治疗剂。该发明特别适用于抗体药物偶联物和双特异性及三特异性抗体衍生物。
  • [EN] CHANNEL PROTEIN ACTIVATABLE LIPOSOMES<br/>[FR] LIPOSOMES ACTIVABLES PAR DES PROTÉINES DE CANAL
    申请人:TAGWORKS PHARMACEUTICALS B V
    公开号:WO2014081300A1
    公开(公告)日:2014-05-30
    Disclosed is a liposome, comprising a lipid bilayer enclosing a cavity, wherein the bilayer comprises a channel protein releasably linked to an eight-membered non-aromatic cyclic alkenylene group, preferably a cyclooctene group, and more preferably a trans-cyclooctene group. The liposomes are used in a kit comprising the liposome, the liposomal membrane of which comprises a channel protein linked to a Trigger, and an Activator for the Trigger, wherein the Trigger comprises the eight- membered non-aromatic cyclic alkenylene group, and the Activator comprises a diene.
    揭示了一种脂质体,包括包裹腔的脂质双层,其中双层包括与八元非芳香环烯链基(优选为环辛烯基,更优选为反式环辛烯基)可释放地连接的通道蛋白。这些脂质体用于一种套装,包括该脂质体,其脂质体膜包括连接到触发器的通道蛋白,以及用于触发器的激活剂,其中触发器包括八元非芳香环烯链基,而激活剂包括二烯。
  • [EN] CHEMICALLY CLEAVABLE GROUP<br/>[FR] GROUPE CLIVABLE PAR VOIE CHIMIQUE
    申请人:TAGWORKS PHARMACEUTICALS B V
    公开号:WO2014081303A1
    公开(公告)日:2014-05-30
    Disclosed is the use of the reactive components of the inverse electron-demand Diels Alder reaction for chemical masking and unmasking in vitro. This can be applied in complex chemical reactions and, particularly in the synthesis of biomolecules, e.g. on solid supports. The reactice components are a dienophile, particularly a trans-cyclooctene, and a diene, particularly a tetrazine.
    本文揭示了逆电子需求Diels-Alder反应的反应性组分用于体外化学掩蔽和解除掩蔽。这可以应用于复杂的化学反应中,特别是在生物分子合成中,例如在固相支持上。反应性组分包括双烯,特别是反式环辛二烯,和二烯,特别是四氮唑。
  • [EN] ACTIVATABLE LIPOSOMES<br/>[FR] LIPOSOME POUVANT ÊTRE ACTIF
    申请人:TAGWORKS PHARMACEUTICALS B V
    公开号:WO2014081299A1
    公开(公告)日:2014-05-30
    Disclosed are reactive liposome, comprising a lipid bilayer enclosing a cavity, wherein the bilayer comprises a linkage to an eight-membered non-aromatic cyclic alkenylene group, preferably a cyclooctene group, and more preferably a trans-cyclooctene group. The liposomes are use in a kit comprising the liposome linked, directly or indirectly, to a Trigger, and an Activator for the Trigger, wherein the Trigger comprises an eight-membered non-aromatic cyclic alkenylene group, and the Activator comprises a diene.
    揭示了一种反应性脂质体,包括一个脂质双层包裹的腔隙,其中该双层包括与一个含有八个成员的非芳香环烯基基团连接的连接,最好是环辛烯基团,更好是反式环辛烯基团。这些脂质体用于一种工具包,该工具包包括直接或间接地与一个触发器连接的脂质体,以及用于触发器的活化剂,其中触发器包括一个含有八个成员的非芳香环烯基基团,而活化剂包括一个二烯。
  • [EN] BIO-ORTHOGONAL DRUG ACTIVATION<br/>[FR] ACTIVATION DE MÉDICAMENT BIO-ORTHOGONALE
    申请人:TAGWORKS PHARMACEUTICALS B V
    公开号:WO2014081301A1
    公开(公告)日:2014-05-30
    Disclosed is a kit for the administration and activation of a Prodrug. The kit comprises a Masking Moiety linked, directly or indirectly, to a Trigger moiety, which in turn is linked to a Drug, and an Activator for the Trigger moiety. The Trigger moiety comprises a dienophile and the Activator comprises a diene, whereby the dienophile is an eight-membered non- aromatic cyclic alkenylene group, preferably a cyclooctene group, and more preferably a trans-cyclooctene group. The Trigger and the Activator undergo a fast, bio-orthogonal reaction resulting in the release of the Masking Moiety, and activation of the drug.
    揭示了一种用于给予和激活前药的工具包。该工具包包括一个掩蔽基团,直接或间接地连接到一个触发基团,该触发基团又连接到一种药物,以及一个用于触发基团的激活剂。触发基团包括一个二烯烃,激活剂包括一个二烯,其中二烯烃是一个八元非芳香环烯基团,优选为环辛烯基团,更优选为反式环辛烯基团。触发基团和激活剂经历一个快速的生物正交反应,导致掩蔽基团的释放和药物的激活。
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