(S)-methyl 4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate | 1383714-46-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (S)-methyl 4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate
• 英文别名: (S)-methyl 4-(4-(4-(4-(7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-8-yloxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate；methyl (S)-4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-benzo[e]pyrrolo[1,2-a][1,4]diazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate；KMR-28-35；methyl 4-[4-[[4-[4-[[(6aS)-2-methoxy-11-oxo-6a,7,8,9-tetrahydropyrrolo[2,1-c][1,4]benzodiazepin-3-yl]oxy]butanoylamino]-1-methylpyrrole-2-carbonyl]amino]phenyl]-1-methylpyrrole-2-carboxylate
• CAS: 1383714-46-2
• 化学式: C₃₆H₃₈N₆O₇
• 分子量: 666.734
• InChiKey: OVVDVKXCZRNFHP-SANMLTNESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  49
• 可旋转键数：
  12
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  146
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (S)-methyl 4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate 在 palladium 10% on activated carbon 、 甲酸铵 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 16.0h， 以46%的产率得到methyl (S)-4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,10,11,11a-hexahydro-1H-benzo[e]pyrrolo[1,2-a][1,4]diazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate
  参考文献：
  名称：

  [EN] POLYCYCLIC AMIDES AS CYTOTOXIC AGENTS
  [FR] AMIDES POLYCYCLIQUES SERVANT D'AGENTS CYTOTOXIQUES

  摘要：

  该发明涉及公式(I)的化合物；或其药学上可接受的盐、溶剂合物、互变异构体、立体异构体或它们的混合物；其中融合环基团是非烷基化基团；这些化合物可用作药物，特别是用作抗体药物结合物中的药物，以及用于治疗增殖性疾病、细菌感染、疟疾感染和炎症。

  公开号：

  WO2020049286A1
• 作为产物：
  描述：

  1-(4-bromo-1-methyl-1H-pyrrol-2-yl)-2,2,2-trichloroethan-1-one 在 盐酸 、 4-二甲氨基吡啶 、 四(三苯基膦)钯 、 硫酸 、 potassium carbonate 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 1,4-二氧六环 、 甲醇 、 乙醇 、 水 、 甲苯 为溶剂， 生成 (S)-methyl 4-(4-(4-(4-((7-methoxy-5-oxo-2,3,5,11a-tetrahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl)oxy)butanamido)-1-methyl-1H-pyrrole-2-carboxamido)phenyl)-1-methyl-1H-pyrrole-2-carboxylate
  参考文献：
  名称：

  Mechanistic insight into the repair of C8-linked pyrrolobenzodiazepine monomer-mediated DNA damage

  摘要：

  我们对吡咯并苯并二氮杂环（PBD）单体的作用方式的理解仍不完整。这项研究揭示了PBD单体在细菌中引起DNA损伤的潜力，并确定了修复这些PBD加合物所涉及的机制。

  DOI：

  10.1039/d2md00194b

文献信息

• [EN] PYRROLOBENZODIAZEPINES<br/>[FR] PYRROLOBENZODIAZÉPINES
  申请人：SPIROGEN SARL

  公开号：WO2013164593A1

  公开（公告）日：2013-11-07

  Pyrrolobenzodiazepine (PBDs) having a (1-methyl-1H-pyrrol-3- yl)phenyl based amino residue were found to be highly effective compounds having improved cytotoxicity ad DNA binding properties.

  发现具有（1-甲基-1H-吡咯-3-基）苯基氨基残基的吡咯苯并二氮杂环烃（PBDs）是具有改善的细胞毒性和DNA结合性能的高效化合物。
• PYRROLOBENZODIAZEPINES
  申请人：SPIROGEN SÀRL

  公开号：US20150133435A1

  公开（公告）日：2015-05-14

  Pyrrolobenzodiazepine (PBDs) having a (1-methyl-1H-pyrrol-3-yl)phenyl based amino residue were found to be highly effective compounds having improved cytotoxicity ad DNA binding properties.

  发现具有基于(1-甲基-1H-吡咯-3-基)苯基氨基残基的吡咯并苯二氮平（PBDs）是高效化合物，具有改善的细胞毒性和DNA结合性能。
• Pyrrolobenzodiazepines as antiproliferative agents
  申请人：MEDIMMUNE LIMITED

  公开号：US09376440B2

  公开（公告）日：2016-06-28

  Novel pyrrolobenzodiazepines (PBDs) having a (1-methyl-1H-pyrrol-3-yl)phenyl based amino acid residue and use thereof as antiproliferative agents are disclosed herein.

  本发明揭示了具有（1-甲基-1H-吡咯-3-基）苯基氨基酸残基的新型吡咯苯并二氮杂环类化合物（PBDs），并将其用作抗增殖剂。
• GC-Targeted C8-Linked Pyrrolobenzodiazepine–Biaryl Conjugates with Femtomolar in Vitro Cytotoxicity and in Vivo Antitumor Activity in Mouse Models
  作者：Khondaker M. Rahman、Paul J. M. Jackson、Colin H. James、B. Piku Basu、John A. Hartley、Maria de la Fuente、Andreas Schatzlein、Mathew Robson、R. Barbara Pedley、Chris Pepper、Keith R. Fox、Philip W. Howard、David E. Thurston

  DOI：10.1021/jm301882a

  日期：2013.4.11

  DNA binding 4-(1-methyl-1H-pyrrol-3-yl)-benzenamine (MPB) building blocks have been developed that span two DNA base pairs with a strong preference for GC-rich DNA. They have been conjugated to a pyrrolo[2,1-c][1,4]benzodiazepine (PBD) molecule to produce C8-linked PBD MPB hybrids that can stabilize GC-rich DNA by up to 13-fold compared to AT-rich DNA. Some have subpicomolar IC50 values in human tumor cell lines and in primary chronic lymphocytic leukemia cells, while being up to 6 orders less cytotoxic in the non-tumor cell line WI38, suggesting that key DNA sequences may be relevant targets in these ultrasensitive cancer cell lines. One conjugate, 7h (KMR-28-39), which has femtomolar activity in the breast cancer cell line MDA-MB-231, has significant dose-dependent antitumor activity in MDA-MB-231 (breast) and MIA PaCa-2 (pancreatic) human tumor xenograft mouse models with insignificant toxicity at therapeutic doses. Preliminary studies suggest that 7h may sterically inhibit interaction of the transcription factor NF-kappa B with its cognate DNA binding sequence.
• POLYCYCLIC AMIDES AS CYTOTOXIC AGENTS
  申请人：FEMTOGENIX LIMITED

  公开号：US20210371413A1

  公开（公告）日：2021-12-02

  The invention relates to a compound of formula (I): or pharmaceutically acceptable salts, solvates, tautomers, stereoisomers or mixtures thereof; wherein the fused ring moiety is a non-alkylating moiety; and wherein the compounds are useful as medicaments, in particular for use as a drug in an antibody-drug conjugate and in the treatment of a proliferative disease, a bacterial infection, a malarial infection and inflammation.