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[(2E)-cyclooct-2-en-1-yl] N-methyl-N-naphthalen-1-ylcarbamate

中文名称
——
中文别名
——
英文名称
[(2E)-cyclooct-2-en-1-yl] N-methyl-N-naphthalen-1-ylcarbamate
英文别名
——
[(2E)-cyclooct-2-en-1-yl] N-methyl-N-naphthalen-1-ylcarbamate化学式
CAS
——
化学式
C20H23NO2
mdl
——
分子量
309.4
InChiKey
BDGXLOBZJNVGEZ-LFYBBSHMSA-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):
    5.5
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [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基基团,而活化剂包括一个二
  • [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烃,激活剂包括一个二,其中二烃是一个八元非芳香环基团,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。
  • CHEMICALLY CLEAVABLE GROUP
    申请人:TAGWORKS PHARMACEUTICALS B.V.
    公开号:US20150344514A1
    公开(公告)日:2015-12-03
    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 reactive components are a dienophile, particularly a trans-cyclooctene, and a diene, particularly a tetrazine.
    本发明揭示了在体外使用反电子需求Diels-Alder反应的反应组分进行化学遮蔽和解除遮蔽的方法。这可以应用于复杂的化学反应中,特别是在生物分子的合成中,例如在固体支持体上。反应组分是二丙烯,特别是反式-环辛烯,和二,特别是四唑
  • BIO-ORTHOGONAL DRUG ACTIVATION
    申请人:TAGWORKS PHARMACEUTICALS B.V.
    公开号:US20150297741A1
    公开(公告)日:2015-10-22
    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.
    本发明揭示了一种用于前药管理和激活的套件。该套件包括一个与触发物质直接或间接连接的掩蔽基团,该触发物质又连接到药物,以及触发物质的活化剂。触发物质包括二亚甲基丙烯酰基,活化剂包括二,其中二亚甲基丙烯酰基是一种八元非芳香环基基团,优选为环辛烯基团,更优选为反式环辛烯基团。触发物质和活化剂经历快速的生物正交反应,导致掩蔽基团的释放和药物的激活。
  • Chemically cleavable group
    申请人:Tagworks Pharmaceuticals B.V.
    公开号:US10927139B2
    公开(公告)日:2021-02-23
    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 reactive components are a dienophile, particularly a trans-cyclooctene, and a diene, particularly a tetrazine.
    本发明公开了利用反电子需求 Diels Alder 反应的反应组分进行体外化学掩蔽和解除掩蔽的方法。这可用于复杂的化学反应,特别是生物大分子的合成,例如在固体支持物上的合成。反应组分是亲二(尤其是反式环辛烯)和二(尤其是四嗪)。
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