4',6-双脒基-2-苯基吲哚 | 47165-04-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 4',6-双脒基-2-苯基吲哚
• 中文别名: 4ˊ,6-二脒基-2-苯基吲哚二盐酸盐；二盐酸-4,6-二脒基-2-苯基吲哚；盐酸-4,6-二脒基-2-苯基吲哚；DAPI
• 英文名称: 4',6-diamidino-2-phenylindole
• 英文别名: DAPI；4′,6-diamidino-2-phenylindole；4’,6-diamidino-2-phenylindole；2-(4-carbamimidoylphenyl)-1H-indole-6-carboximidamide
• CAS: 47165-04-8
• 化学式: C₁₆H₁₅N₅
• 分子量: 277.329
• InChiKey: FWBHETKCLVMNFS-UHFFFAOYSA-N

物化性质

• 沸点：
  545.4±60.0 °C(Predicted)
• 密度：
  1.41±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  116
• 氢给体数：
  5
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4',6-双脒基-2-苯基吲哚 在 甲酸 、 palladium 10% on activated carbon 、 氢气 、 碳酸氢铵 作用下， 以 水 、 丙酮 为溶剂， 生成 5-[3-[[6-carbamimidoyl-2-(4-carbamimidoylphenyl)-1H-indol-3-yl]methyl]-4-hydroxyanilino]-5-oxopentanoic acid
  参考文献：
  名称：

  BIFUNCTIONAL PHOTOCROSSLINKING PROBES FOR COVALENT CAPTURE OF PROTEIN-NUCLEIC ACID COMPLEXES IN CELLS

  摘要：

  A new class of molecular probes is provided for real, efficient, stable, and selective capture of protein-nucleic acid complexes inside cells. The molecular probes have a nucleic acid-binding functional group and a photo-reactive diazirine based functional group, separated by a linker of a selected length or with a multi-arm core, thereby generating a photocrosslink between nucleic acids and proteins in close proximity. This is useful in various chromatin research, including the study of interactions between transcription factors and DNA.

  公开号：

  WO2024015963A2
• 作为产物：
  描述：

  ethyl 2-[4-(C-ethoxycarbonimidoyl)phenyl]-1H-indole-6-carboximidate 在 氨 作用下， 以 乙醇 为溶剂， 生成 4',6-双脒基-2-苯基吲哚
  参考文献：
  名称：

  Amidine derived inhibitors of acid-sensing ion channel-3 (ASIC3)

  摘要：

  A series of indole amidines modified at the 2-position of the indole ring were evaluated as inhibitors of Acid-Sensing Ion Channel-3 (ASIC3), a novel target for the treatment of chronic pain. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.06.021

文献信息

• COMPOSITIONS AND METHODS FOR TREATING NEURODEGENERATIVE DISEASE
  申请人：COGNITION THERAPEUTICS, INC.

  公开号：US20170197977A9

  公开（公告）日：2017-07-13

  This invention relates to novel diarylamino compounds that bind to the sigma-2 receptor, to pharmaceutical compositions comprising such compounds, and to methods for inhibiting or restoring synapse loss in neuronal cells, modulating a membrane trafficking change in neuronal cells, and treating cognitive decline and neurodegenerative diseases and disorders therewith.

  这项发明涉及与sigma-2受体结合的新型二芳胺化合物，包括这种化合物的药物组合物，以及用于抑制或恢复神经元细胞中突触丢失，调节神经元细胞中膜运输变化，并用于治疗认知衰退和神经退行性疾病和障碍的方法。
• Chemical inducers of neurogenesis
  申请人：Schneider Jay

  公开号：US20090036451A1

  公开（公告）日：2009-02-05

  The present invention relates to compounds and methods for inducing neuronal differentiation in normal neural stem cells and brain cancer stem cells. The methods may take place in vitro, such as in isolates from the adult mammalian brain, or in vivo. Compounds and methods described herein may find use in the treatment of neurodegenerative and psychiatric diseases, the repair and regeneration of the nervous system, and in treatment of neurologic malignancy.

  本发明涉及化合物和方法，用于诱导正常神经干细胞和脑癌干细胞的神经元分化。这些方法可以在体外进行，例如在成年哺乳动物大脑的分离物中，或在体内进行。本文描述的化合物和方法可能在治疗神经退行性和精神疾病、神经系统的修复和再生以及神经逻辑恶性肿瘤的治疗中发挥作用。
• CLICKABLE POLYOXETANE CARRIER FOR DRUG DELIVERY
  申请人：YANG Hu

  公开号：US20150258204A1

  公开（公告）日：2015-09-17

  A polymer is provided, comprising a subunit having the formula: (I), wherein A, B, C, D, a, b, c, d, and p are defined herein. Compositions, methods of making, and methods of use are provided.

  提供一种聚合物，包括具有以下公式的亚单位：(I)，其中A、B、C、D、a、b、c、d和p在此定义。提供了组成物、制备方法和使用方法。
• ASYMMETRIC BIFUNCTIONAL SILYL MONOMERS AND PARTICLES THEREOF AS PRODRUGS AND DELIVERY VEHICLES FOR PHARMACEUTICAL, CHEMICAL AND BIOLOGICAL AGENTS
  申请人：The University of North Carolina at Chapel Hill

  公开号：US20170021030A1

  公开（公告）日：2017-01-26

  Asymmetric bifunctional silyl (ABS) monomers comprising covalently linked pharmaceutical, chemical and biological agents are described. These agents can also be covalently bound via the silyl group to delivery vehicles for delivering the agents to desired targets or areas. Also described are delivery vehicles which contain ABS monomers comprising covalently linked agents and to vehicles that are covalently linked to the ABS monomers. The silyl modifications described herein can modify properties of the agents and vehicles, thereby providing desired solubility, stability, hydrophobicity and targeting.

  描述了包含共价连接的药物、化学和生物试剂的不对称双功能硅基（ABS）单体。这些试剂也可以通过硅基团共价结合到传递载体上，以将试剂传递到所需的靶标或区域。还描述了包含共价连接试剂的ABS单体的传递载体，以及与ABS单体共价连接的载体。本文描述的硅基修饰可以修改试剂和载体的性质，从而提供所需的溶解性、稳定性、疏水性和靶向性。
• [EN] INHIBITORS OF LYSINE SPECIFIC DEMETHYLASE-1<br/>[FR] INHIBITEURS DE LA DÉMÉTHYLASE-1 SPÉCIFIQUE DE LA LYSINE
  申请人：QUANTICEL PHARMACEUTICALS INC

  公开号：WO2016003917A1

  公开（公告）日：2016-01-07

  The present invention relates generally to compositions and methods for treating cancer and neoplastic disease. Provided herein are substituted heterocyclic derivative compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful for inhibition of lysine specific demethylase-1. Furthermore, the subject compounds and compositions are useful for the treatment of cancer, such as prostate cancer, breast cancer, bladder cancer, lung cancer and/or melanoma and the like.

  本发明一般涉及治疗癌症和肿瘤性疾病的组合物和方法。本文提供了替代杂环衍生物化合物和包含该化合物的药物组合物。所述化合物和组合物对赖氨酸特异性去甲基化酶-1的抑制是有用的。此外，所述化合物和组合物对癌症的治疗是有用的，如前列腺癌、乳腺癌、膀胱癌、肺癌和/或黑色素瘤等。