17-Allylaminogeldanamycin

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酰胺类
• 英文名称: 17-Allylaminogeldanamycin
• 英文别名: [13-hydroxy-8,14-dimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-19-(prop-2-enylamino)-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl] carbamate
• 化学式: C₃₁H₄₃N₃O₈
• 分子量: 585.7
• InChiKey: AYUNIORJHRXIBJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  42
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  166
• 氢给体数：
  4
• 氢受体数：
  9

文献信息

• Anti-Tumor Methods Using Multi Drug Resistance Independent Synthetic HSP90 Inhibitors
  申请人：Zhang Hong

  公开号：US20070105874A1

  公开（公告）日：2007-05-10

  The present invention provides a method of treating an individual having an HSP90 mediated disorder comprising administering to said individual a pharmaceutical composition comprising a pharmaceutically effective amount of a synthetic heterocyclic HSP90 inhibitor, wherein the activity of the HSP90 inhibitor is substantially independent of multi drug resistance. In one embodiment, the activity of the HSP90 inhibitor is substantially independent of P-gp and MRP expression.
• METHODS, COMPOSITIONS, AND KITS FOR THE TREATMENT OF CANCER
  申请人：Haggerty Timothy J.

  公开号：US20140335050A1

  公开（公告）日：2014-11-13

  The invention features methods, compositions, and kits for the administration of an HSP90 inhibitor, OBAA, flunarizine, aphidicolin, damnacanthal, dantrolene, or an analog thereof, alone, or in combination with, e.g., a TAA, an antigen-binding scaffold (e.g., an antibody, a soluble T cell receptor, or a chimeric receptor) specific for a TAA, a cell (e.g., a white blood cell that targets a cancer cell), and/or an IFN-β receptor agonist or an IFN-γ receptor agonist, for the treatment of cancer.
• Use of Small Molecule Unfolder Protein Response Modulators to Treat Tumors With Active Sonic Hedgehog (SSH) Signaling Due To Smoothened (SMO) Mutation
  申请人：ST. JUDE CHILDREN'S RESEARCH HOSPITAL

  公开号：US20150320723A1

  公开（公告）日：2015-11-12

  The present invention relates to methods for treating tumors having SMO mutations as well as diagnosing tumors with SMO mutations. The invention relates to methods for the treatment of cancer with ER stress-inducing compounds or UPR inducing compounds. The ER stress-inducing compounds or UPR inducing compounds might fill a clinical need for additional methods of targeting the Hh pathway, either in frontline combination therapy or in salvage therapy for relapsed patients who develop resistance to the available SMO inhibitor and offer a significant advantage over SMO-specific small molecules. Because ER stress modulators and UPR inducing compounds exploit a cellular process that is distinct from the Hh signaling pathway, their efficacy should be unaltered by acquired SMO mutation.
• [EN] USE OF SMALL MOLECULE UNFOLDER PROTEIN RESPONSE MODULATORS TO TREAT TUMORS WITH ACTIVE SONIC HEDGEHOG (SSH) SIGNALING DUE TO SMOOTHENED (SMO) MUTATION<br/>[FR] UTILISATION DE MODULATEURS DE RÉPONSE DE LA PROTÉINE DÉPLIÉE (UPR) À PETITES MOLÉCULES POUR TRAITER DES TUMEURS DONT LA VOIE DE SIGNALISATION SONIC HEDGEHOG (SSH) A ÉTÉ ACTIVÉE EN RAISON D'UNE MUTATION SMOOTHENED (SMO)
  申请人：ST JUDE CHILDRENS RES HOSPITAL

  公开号：WO2014107655A1

  公开（公告）日：2014-07-10

  The present invention relates to methods for treating tumors having SMO mutations as well as diagnosing tumors with SMO mutations. The invention relates to methods for the treatment of cancer with ER stress-inducing compounds or UPR inducing compounds. The ER stress-inducing compounds or UPR inducing compounds might fill a clinical need for additional methods of targeting the Hh pathway, either in frontline combination therapy or in salvage therapy for relapsed patients who develop resistance to the available SMO inhibitor and offer a significant advantage over SMO-specific small molecules. Because ER stress modulators and UPR inducing compounds exploit a cellular process that is distinct from the Hh signaling pathway, their efficacy should be unaltered by acquired SMO mutation.