4-Aza-5-thiatricyclo[5.2.1.0(3,7)]decane, 5,5-dioxo-4-(2-propenoyl)-10,10-dimethyl-

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 4-Aza-5-thiatricyclo[5.2.1.0(3,7)]decane, 5,5-dioxo-4-(2-propenoyl)-10,10-dimethyl-
• 英文别名: 1-(10,10-dimethyl-3,3-dioxo-3λ6-thia-4-azatricyclo[5.2.1.01,5]decan-4-yl)prop-2-en-1-one
• 化学式: C₁₃H₁₉NO₃S
• 分子量: 269.36
• InChiKey: QYWKUFBZHFLMBU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  62.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-Aza-5-thiatricyclo[5.2.1.0(3,7)]decane, 5,5-dioxo-4-(2-propenoyl)-10,10-dimethyl- 、 环戊二烯 以49%的产率得到
  参考文献：
  名称：

  Yamamoto Keiji, Momose Satoru, Funahashi Masakazu, Ebata Satoshi, Ohmura +, Chem. Lett, (1994) N 2, S 198-192

  摘要：

  DOI：

文献信息

• [EN] TRIOXACARCINS, TRIOXACARCIN-ANTIBODY CONJUGATES, AND USES THEREOF<br/>[FR] TRIOXACARCINES, CONJUGUÉS TRIOXACARCINE-ANTICORPS, ET LEURS UTILISATIONS
  申请人：HARVARD COLLEGE

  公开号：WO2014082065A1

  公开（公告）日：2014-05-30

  Provided herein are trioxacarcin-antibody drug conjugates of Formula (A): and pharmaceutically acceptable salts thereof, comprising at least one instance of the group - L1 -(A-L2 )a-B attached thereto, wherein a is an integer between 1 and 10, inclusive, L1 is absent or is a linking group, A is a moiety formed from the reaction of two complimentary groups (X and Y), L2 is absent or is another linking group, and B is an antibody or antibody fragment. Also provided are methods of preparing these antibody-drug conjugates, pharmaceutically acceptable compositions thereof, and methods of their use and treatment. Further provided are precursors to the trioxacarcin-antibody drug conjugates, novel trioxacarcins without an antibody conjugated thereto, pharmaceutical compositions thereof, and methods of their use and treatment.

  本文提供的是Formula（A）的三氧卡西青霉素-抗体药物偶联物及其药学上可接受的盐，其中至少包括一个-L1-（A-L2）a-B的组合，其中a是1到10之间的整数，L1不存在或是一个连接基团，A是由两个互补基团（X和Y）反应形成的基团，L2不存在或是另一个连接基团，B是抗体或抗体片段。还提供了制备这些抗体药物偶联物的方法，其药学上可接受的组成物，以及其使用和治疗的方法。此外，还提供了三氧卡西青霉素-抗体药物偶联物的前体，未与抗体偶联的新型三氧卡西青霉素，其药学上可接受的组成物，以及其使用和治疗的方法。
• Tetrapeptide analogs
  申请人：Chao Bin

  公开号：US20100190688A1

  公开（公告）日：2010-07-29

  Compounds, compositions and methods for treatment of hyperproliferative diseases, such as cancer are provided.

  提供了用于治疗过度增殖性疾病，如癌症的化合物、组合物和方法。
• TRIOXACARCINS AND USES THEREOF
  申请人：Myers Andrew G.

  公开号：US20130150314A1

  公开（公告）日：2013-06-13

  The present invention relates to trioxacarcin compounds of the formula: (I) or pharmaceutically acceptable forms thereof; wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are as defined herein. The present invention also provides processes for preparing such compounds and intermediates thereto; pharmaceutical compositions comprising such compounds; and methods of use and treatment.

  本发明涉及式(I)的三氧卡西林化合物或其药学上可接受的形式；其中R1、R2、R3、R4、R5、R6、R7、R8和R9如本文所定义。本发明还提供制备这种化合物和中间体的过程；包含这种化合物的药物组合物；以及使用和治疗的方法。
• Tripeptides as caspase modulators
  申请人：Idun Pharmaceuticals, Inc.

  公开号：EP2457896A1

  公开（公告）日：2012-05-30

  Compounds, compositions and methods for treatment of hyperproliferative diseases, such as cancer are provided. or a pharmaceutically acceptable derivative thereof, where: M is CO, SO or SO2; R1sand R2s are selected as follows: (i) R1s is hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl or heterocyclyI; and R2s is selected from hydrogen, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl, heterocyclyl, OR11 and NR15R16, or (ii) R 1sand R2s together with the nitrogen atom on which they are substituted form a heterocyclic or heteroaryl ring; R3s, R4s and R5s are each independently selected from (i) or (ii) as follows: (i) R3s is hydrogen or alkyl; R4s is alkyl; and R5s is selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heteroarylium, cycloalkyl, heterocyclyl and NR15R16; (ii )R5s and R3s or R5s and R4s together with the atoms on which they are substituted form heterocyclic or heteroaryl ring and the other of R3s or R4s is selected as (ii); R6s is hydrogen, lower alkyl, lower alkenyl or lower alkynyl; R7s is hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl or heterocyclyl. The other variables are as defined in the claims.

  本研究提供了用于治疗过度增殖性疾病（如癌症）的化合物、组合物和方法。 或其药学上可接受的衍生物、 其中 M 是 CO、SO 或 SO2； R1s 和 R2s 选取如下： (i) R1s 是氢、烷基、烯基、炔基、芳基、杂芳基、环烷基或杂环烷基；R2s 选自氢、烯基、炔基、芳基、杂芳基、环烷基、杂环烷基、 OR11 和 NR15R16，或 (ii) R 1s 和 R2s 与它们被取代的氮原子一起形成杂环或杂芳基环； R3s、R4s 和 R5s 各自独立地选自如下的 (i) 或 (ii)： (i) R3s 是氢或烷基；R4s 是烷基；R5s 选自氢、烷基、烯基、炔基、芳基、杂芳基、杂芳脲基、环烷基、杂环烷基和 NR15R16； (ii)R5s 和 R3s 或 R5s 和 R4s 与它们被取代的原子一起形成杂环或杂芳基环，且 R3s 或 R4s 中的另一个选为(ii)； R6s 是氢、低级烷基、低级烯基或低级炔基； R7s 是氢、烷基、烯基、炔基、芳基、杂芳基、环烷基或杂环烷基。 其他变量如权利要求中所定义。
• Trioxacarcins, trioxacarcin#antibody conjugates, and uses thereof
  申请人：President and Fellows of Harvard College

  公开号：US10639381B2

  公开（公告）日：2020-05-05

  Provided herein are trioxacarcin-antibody drug conjugates of Formula (A): and pharmaceutically acceptable salts thereof, comprising at least one instance of the group -L1-(A-L2)a-B attached thereto, wherein a is an integer between 1 and 10, inclusive, L1 is absent or is a linking group, A is a moiety formed from the reaction of two complimentary groups (X and Y), L2 is absent or is another linking group, and B is an antibody or antibody fragment. Also provided are methods of preparing these antibody-drug conjugates, pharmaceutically acceptable compositions thereof, and methods of their use and treatment. Further provided are precursors to the trioxacarcin-antibody drug conjugates, novel trioxacarcins without an antibody conjugated thereto, pharmaceutical compositions thereof, and methods of their use and treatment.

  本文提供的是式 (A) 的三氧羰基霉素-抗体药物共轭物： 及其药学上可接受的盐，包含至少一个连接在其上的基团-L1-(A-L2)a-B 的实例，其中 a 是 1 至 10（包括 10）之间的整数，L1 不存在或为连接基团，A 是由两个互补基团（X 和 Y）反应形成的分子，L2 不存在或为另一个连接基团，B 是抗体或抗体片段。此外，还提供了制备这些抗体-药物共轭物的方法、其药学上可接受的组合物及其使用和治疗方法。此外，还提供了三氧嘧啶-抗体药物共轭物的前体、不含抗体的新型三氧嘧啶、其药用组合物及其使用和治疗方法。