6-ethoxycarbonyloxy-5,7-dihydro-indolo-[2,3-b]carbazole | 666752-30-3

• 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
• 英文名称: 6-ethoxycarbonyloxy-5,7-dihydro-indolo-[2,3-b]carbazole
• 英文别名: SR 13650；Carbonic acid, 5,7-dihydroindolo[2,3-b]carbazol-6-yl ethyl ester；5,7-dihydroindolo[2,3-b]carbazol-6-yl ethyl carbonate
• CAS: 666752-30-3
• 化学式: C₂₁H₁₆N₂O₃
• 分子量: 344.37
• InChiKey: HHLRSANYYAEVCV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  67.1
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  Ditert-butyl 6-ethoxycarbonyloxyindolo[2,3-b]carbazole-5,7-dicarboxylate 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 以0.39 g的产率得到6-ethoxycarbonyloxy-5,7-dihydro-indolo-[2,3-b]carbazole
  参考文献：
  名称：

  Computer-Aided Rational Drug Design:  A Novel Agent (SR13668) Designed to Mimic the Unique Anticancer Mechanisms of Dietary Indole-3-Carbinol to Block Akt Signaling

  摘要：

  Indole-3-carbinol (I3C) is a naturally occurring anticancer agent and has entered clinical trials for cancer prevention. However, the clinical development of I3C has been impeded by its poor metabolic profile. The active components of I3C were used to develop a novel class of indole analogs to optimize I3C's anticancer actions, including blocking growth factor-stimulated Akt activation. The most promising of these analogs, SR13668, exhibited potent oral anticancer activity against various cancers and no significant toxicity.

  DOI：

  10.1021/jm070040e

文献信息

• Analogs of indole-3-carbinol metabolites as chemotherapeutic and chemopreventive agents
  申请人：——

  公开号：US20040043965A1

  公开（公告）日：2004-03-04

  Novel compounds useful as chemotherapeutic and chemopreventive agents are provided. The compounds are analogs of indole-3-carbinol metabolites wherein the structures and substituents of the compounds are selected to enhance the compounds' overall efficacy, particularly with respect to therapeutic activity, oral bioavailability, long-term safety, patient tolerability, and therapeutic window. The compounds are useful not only in treatment of cancer but also in prevention of cancer. One preferred class of the novel compounds have the structure of formula (I) 1 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , and R 12 are defined herein. Pharmaceutical compositions are provided as well, as are methods of synthesis and use.

  提供了作为化疗和化学预防剂有用的新化合物。这些化合物是吲哚-3-甲醇代谢物的类似物，其中化合物的结构和取代基被选择以增强化合物的整体功效，特别是在治疗活性、口服生物利用度、长期安全性、患者耐受性和治疗窗口方面。这些化合物不仅在癌症治疗中有用，而且在癌症预防中也有用。一类首选的新化合物具有以下结构式（I） 1 其中R 1 、R 2 、R 3 、R 4 、R 5 、R 6 、R 7 、R 8 、R 9 、R 10 、R 11 和R 12 在此定义。还提供了药物组合物，以及合成和使用方法。
• Analogs of Indole-3-Carbinol and Their Use as Agents Against Infection
  申请人：Jong Ling

  公开号：US20100069355A1

  公开（公告）日：2010-03-18

  Compounds useful as antibacterial agents are provided. The compounds are analogs of indole-3-carbinol and have a backbone selected from dihydroindolo[2,3-b]carbazole, 2,2′-diindolylmethane, 2′,3-diindolylmethane, and 3,3′-diindolylmethane. The compounds are useful therapeutic and prophylactic treatment of bacterial infections in mammals. Methods of synthesis of the compounds are provided, as are pharmaceutical compositions containing the compounds.

  提供了作为抗菌剂有用的化合物。这些化合物是吲哚-3-甲醇的类似物，具有从二氢吲哚并[2,3-b]咔唑，2,2′-二吲哚甲烷，2′,3-二吲哚甲烷和3,3′-二吲哚甲烷中选择的骨架。这些化合物对哺乳动物的细菌感染的治疗和预防治疗有用。提供了合成这些化合物的方法，以及含有这些化合物的药物组合物。
• Combined use of cruciferous indoles and chelators for the treatment of papilloma virus-related conditions
  申请人：Zeligs A. Michael

  公开号：US20050063903A1

  公开（公告）日：2005-03-24

  This abstract describes eliminating the need for cutting up manufactured synthetic filament polymer yarns (for examples, nylon and Kevlar) into wool and linen lengths and respinning these again into yarns approaching wool and linen like wear properties in clothing and other textiles at significant reductions in production costs accomplished by using laser pierced holes in the plates of and adding continuous wave or pulsed sonic generators to the rear of spinneret housings through which viscous polymer fluids flow both of which produce surface irregularities in the yarns (longitudinal and circumferential ridges in valleys) in the spun continuous filaments approaching wear properties of natural wool and linen.

  该摘要描述了通过在纺丝器壳体后部添加连续波或脉冲声波发生器，并在纺丝器板上使用激光穿孔孔，消除了将制造的合成纤维聚合物纱线（例如尼龙和凯夫拉）切成羊毛和亚麻长度，并重新纺成具有羊毛和亚麻类服装和其他纺织品的纱线的需要，从而在生产成本上实现了显着的降低。这两种方法都会在连续纤维中产生表面不规则性（纵向和周向脊和谷），使其接近天然羊毛和亚麻的耐磨性质。
• Analogs of Indole-3-Carbinol Metabolites as Chemotherapeutic and Chemopreventive Agents
  申请人：JONG Ling

  公开号：US20090023796A1

  公开（公告）日：2009-01-22

  Novel compounds useful as chemotherapeutic and chemopreventive agents are provided. The compounds are analogs of indole-3-carbinol metabolites wherein the structures and substituents of the compounds are selected to enhance the compounds' overall efficacy, particularly with respect to therapeutic activity, oral bioavailability, long-term safety, patient tolerability, and therapeutic window. The compounds are useful not only in treatment of cancer but also in prevention of cancer. One preferred class of the novel compounds has the structure of formula (IV) wherein: R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 5A , R 6A , R 7A , R 8A , R 22 and R 23 are defined herein. Pharmaceutical compositions are provided as well, as are methods of synthesis and use.

  提供了一种作为化疗和化学预防剂的新化合物。这些化合物是吲哚-3-甲醇代谢产物的类似物，其中这些化合物的结构和取代基被选择以增强这些化合物的整体功效，特别是治疗活性、口服生物利用度、长期安全性、患者耐受性和治疗窗口方面的功效。这些化合物不仅在癌症治疗方面有用，而且在癌症预防方面也有用。其中一类优选的新化合物具有公式（IV）的结构，其中：R1、R2、R3、R4、R5、R6、R7、R8、R5A、R6A、R7A、R8A、R22和R23在此被定义。此外，还提供了制药组合物、合成和使用方法。
• Analogs of indole-3-carbinol metabolites as chemotherapeutic and chemopreventative agents
  申请人：SRI International

  公开号：EP1623985A2

  公开（公告）日：2006-02-08

  Novel compounds useful as chemotherapeutic and chemopreventative agents are provided. The compounds are analogs of indole-3-carbinol metabolites wherein the structures and substituents of the compounds are selected to enhance the compounds' overall efficacy, particularly with respect to therapeutic activity, oral bioavailability, long-term safety, patient tolerability, and therapeutic window. The compounds are useful not only in treatment of cancer but also in prevention of cancer. One preferred class of the novel compounds has the structure of formula (I), wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 and R12 are defined herein. Pharmacetical compositions are provided as well, as are methods of synthesis and use.

  本研究提供了可用作化疗和化疗预防剂的新型化合物。这些化合物是吲哚-3-甲醇代谢物的类似物，其中化合物的结构和取代基的选择是为了提高化合物的整体疗效，特别是在治疗活性、口服生物利用度、长期安全性、患者耐受性和治疗窗口方面。这些化合物不仅可用于治疗癌症，还可用于预防癌症。一类优选的新型化合物具有式 (I) 结构，其中 R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R11 和 R12 在此定义。此外，还提供了药用组合物以及合成和使用方法。