1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine | 304863-12-5

• 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: 1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine
• 英文别名: N-[4-[4-[4-[ethyl-(2,4,6-trimethylphenyl)sulfonylamino]butyl-(2,4,6-trimethylphenyl)sulfonylamino]butyl-(2,4,6-trimethylphenyl)sulfonylamino]butyl]-2,4,6-trimethylbenzenesulfonamide
• CAS: 304863-12-5
• 化学式: C₅₀H₇₄N₄O₈S₄
• 分子量: 987.424
• InChiKey: LUVZZPLOIIOBPP-UHFFFAOYSA-N

物化性质

• 沸点：
  1008.7±75.0 °C(Predicted)
• 密度：
  1.189±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  10.3
• 重原子数：
  66
• 可旋转键数：
  24
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.52
• 拓扑面积：
  192
• 氢给体数：
  1
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine 在 sodium hydride 、 一水合肼 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 5,10,15,20-tetrakis(mesitylenesulfonyl)-5,10,15,20-tetraaza-1-docosamine
  参考文献：
  名称：

  SYNTHESIS AND GROWTH REGULATORY ACTIVITY OF A PROTOTYPE MEMBER OF A NEW FAMILY OF AMlNOTHIOL RADIOPROTECTORS

  摘要：

  报道了PrC-210氨硫醇，3-(甲氨基)-2-((甲氨基)甲基)丙烷-1-硫醇及其多胺和硫化多胺前体的合成、生长抑制和放射防护活性。所有分子均显著抑制培养的正常人类成纤维细胞的生长。具有ROS清除硫基团和带正电的烷基胺骨架的组合提供了最具放射防护性的氨硫醇分子。

  公开号：

  US20140107216A1
• 作为产物：
  描述：

  N-ethylmesitylenesulfonamide 在 sodium hydride 、 一水合肼 、 三乙胺 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 生成 1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine
  参考文献：
  名称：

  SYNTHESIS AND GROWTH REGULATORY ACTIVITY OF A PROTOTYPE MEMBER OF A NEW FAMILY OF AMlNOTHIOL RADIOPROTECTORS

  摘要：

  报道了PrC-210氨硫醇，3-(甲氨基)-2-((甲氨基)甲基)丙烷-1-硫醇及其多胺和硫化多胺前体的合成、生长抑制和放射防护活性。所有分子均显著抑制培养的正常人类成纤维细胞的生长。具有ROS清除硫基团和带正电的烷基胺骨架的组合提供了最具放射防护性的氨硫醇分子。

  公开号：

  US20140107216A1

文献信息

• [EN] PORPHYRIN-POLYAMINE CONJUGATES FOR CANCER THERAPY<br/>[FR] CONJUGUE DE PORPHYRINE-POLYAMINE POUR LA CANCEROTHERAPIE
  申请人：SLIL BIOMEDICAL CORP

  公开号：WO2004002991A1

  公开（公告）日：2004-01-08

  Porphyrin-polyamine conjugate compounds are disclosed which have anticancer and antitumor effects. The porphyrin moiety selectively localizes in tumors, while the polyamine moiety serves as a cytotoxic agent. Methods of making and using the porphyrin-polyamine conjugate compounds are also disclosed.

  揭示了具有抗癌和抗肿瘤效果的卟啉-聚胺共轭化合物。卟啉基团选择性地定位在肿瘤中，而聚胺基团作为细胞毒性剂。还公开了制备和使用卟啉-聚胺共轭化合物的方法。
• SYNTHESIS AND GROWTH REGULATORY ACTIVITY OF A PROTOTYPE MEMBER OF A NEW FAMILY OF AMlNOTHIOL RADIOPROTECTORS
  申请人：Fahl William E.

  公开号：US20140107216A1

  公开（公告）日：2014-04-17

  The synthesis, growth inhibition and radioprotective activity of the PrC-210 aminothiol, 3-(methyl-amino)-2-((methylamino)methyl)propane-1-thiol, and its polyamine and thiolated polyamine progenitors are reported. All of the molecules significantly inhibited growth of cultured normal human fibroblasts. The combination of an ROS-scavenging thiol group and a positively charged alkyl-amine backbone provided the most radioprotective aminothiol molecule.

  报道了PrC-210氨硫醇，3-(甲氨基)-2-((甲氨基)甲基)丙烷-1-硫醇及其多胺和硫化多胺前体的合成、生长抑制和放射防护活性。所有分子均显著抑制培养的正常人类成纤维细胞的生长。具有ROS清除硫基团和带正电的烷基胺骨架的组合提供了最具放射防护性的氨硫醇分子。
• Cyclopropane-Containing Polyamine Analogues Are Efficient Growth Inhibitors of a Human Prostate Tumor Xenograft in Nude Mice
  作者：Benjamin Frydman、Andrei V. Blokhin、Sara Brummel、George Wilding、Yulia Maxuitenko、Aparajita Sarkar、Subhra Bhattacharya、Dawn Church、Venodhar K. Reddy、John A. Kink、Laurence J. Marton、Aldonia Valasinas、Hirak S. Basu

  DOI：10.1021/jm030175u

  日期：2003.10.1

  Polyamine analogues 7, 10, 18, 27, and 32 containing cyclopropane rings were obtained by chemical synthesis. Their antineoplastic activities were assessed against the cultured human prostate tumor cell lines DU-145, DuPro, and PC-3. Decamines 32 and 27 exhibited variable levels of cytotoxicity against all three cell lines, while 7, 10, and 18 were efficacious against DU-145 and DuPro. Maximum tolerated doses (MTD) for all five compounds in a NCr-nu mouse model were determined at dosing schedules of q1d x 5 (ip) in two cycles with a break of 10 days between cycles. Their antitumor efficacies were then tested against DU-145 tumor xenografts in mice treated with all five agents at their respective MTDs. In addition, the efficacies of 7 and 10 against the same tumor xenograft were assessed at doses below their respective MTDs. In all experiments, administration began two weeks after tumor implantation. All compounds efficiently inhibited tumor growth for up to 50 days postimplantation, with negligible animal body weight loss. Tetramine 10 and hexamine 18 were the most efficient among the five analogues in arresting tumor growth. Tetramine 10 containing two cyclopropane rings had the lowest systemic toxicity as reflected in animal body weight loss. It was further assessed at a weekly administration regimen of (q1w x 4) in two cycles with a four-week break between the cycles. At this dosing schedule, 10 again efficiently arrested tumor growth with negligible effect on animal body weight. Tetramine 10 also arrested the growth of large tumors (ca. 2000 mm(3)) treated 66 days postimplantation. Studies on the metabolism of 10 showed that it accumulates in tumor within 6 h after the end of administration and reached a maximum level 72 h after cessation of dosing. Intracellular concentrations of 10 in liver and kidney were much smaller when compared to those in the tumor when measured 72 h after cessation of dosing. In liver and kidney, the deethyl metabolites of 10 accumulated over a 96 h period after cessation of dosing.
• Long-chain polyamines (oligoamines) exhibit strong cytotoxicities against human prostate cancer cells
  作者：Aldonia Valasinas、Venodhar K Reddy、Andrei V Blokhin、Hirak S Basu、Subhra Bhattacharya、Aparajita Sarkar、Laurence J Marton、Benjamin Frydman

  DOI：10.1016/s0968-0896(03)00453-x

  日期：2003.9

  N-alpha,N-omega-bis(ethyl) octamine SL-11160, decamine SL-11159, dodecamine SL-11226, and tetradecamine SL-11175 were chemically synthesized. We called this class of compounds 'oligoamines'. In these compounds, each -NH2+ residue is separated by four CH2 residues. trans-Unsaturation was also introduced into the center of the oligoamine chain resulting in the trans-octamine SL-11158, trans-decamine SL-11144, trans-dodecamine SL-11172 and trans-tetradecamine SL-11227. cis-Unsaturation gave the cisoctamine SL-11157 and cis-decamine SL-11150. When assayed for their growth inhibitory effect against four human prostate cancer cell lines LnCap, DU-145, DuPro, and PC-3 by a MTT assay, the ID50 values were less than 1 muM in all four cell lines. On day 6 of treatment, 2 muM SL-11159, SL-11144 and SL-11175 killed over five logs of DuPro cells while SL-11172 killed over four logs as determined by a colony forming efficiency (CFE) assay. In addition, SL-11159, SL-11226 and SL-11227 killed four logs of PC-3 cells. PC-3 cells are generally resistant to shorter chain polyamine analogues. Such a level of cytotoxicity in any of the prostate tumor cell lines has not been observed for any other polyamine analogues tested thus far. The DU-145 cell line was too sensitive to oligoamines to perform a CFE analysis and the DuPro cell line was too sensitive to SL-11227 treatment to obtain reproducible CFE data. Interestingly, all 10 oligoamines were efficient DNA aggregators in a cell-free system and their cytotoxicities generally parallel their capacities to aggregate DNA. (C) 2003 Elsevier Ltd. All rights reserved.
• US7314959B2
  申请人：——

  公开号：US7314959B2

  公开（公告）日：2008-01-01