• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

吡咯并咪唑醌类化合物在海绵动物齐氏海绵属中的抗肿瘤活性及分布

Antitumor activity and distribution of pyrroloiminoquinones in the sponge genus Zyzzya.

作者信息

Dijoux Marie-Geneviève, Schnabel Peter C, Hallock Yali F, Boswell Jamie L, Johnson Tanya R, Wilson Jennifer A, Ireland Chris M, van Soest Rob, Boyd Michael R, Barrows Louis R, Cardellina John H

机构信息

Laboratory of Drug Discovery Research and Development, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute-Frederick Cancer Research & Development Center, Frederick, MD 21702-1201, USA.

出版信息

Bioorg Med Chem. 2005 Nov 1;13(21):6035-44. doi: 10.1016/j.bmc.2005.06.019.

DOI:10.1016/j.bmc.2005.06.019
PMID:16009557
Abstract

A detailed analysis of four different collections of the sponge genus Zyzzya yielded nine pyrroloiminoquinones of the makaluvamine, batzelline, and isobatzelline/damirone classes. Dereplication analyses of additional Zyzzya extracts did not disclose more potent or additional new compounds. Comparative testing of these compounds in the National Cancer Institute's 60 cell line human tumor screen revealed varying levels of potency and differential cytotoxicity, apparently related to the unsaturation levels in and substitution patterns on the core ring system. Further studies on the topoisomerase II-mediated DNA cleavage were conducted. Reductive activation of the pyrroloiminoquinones led to DNA damage in vitro, which correlated with half wave potentials and reversibility parameters. DNA damage could be abrogated by ascorbate. Fluorescence displacement was used to measure intercalation with DNA; intercalation efficiency did not correlate with DNA-damaging proficiency. Makaluvamine H (5) emerged as the most potent and differential of our isolates, roughly comparable to makaluvamines C (in vitro) and I (in vivo). 3,7-Dimethyl guanine was isolated from one of the Zyzzya collections and from the sponge Latrunculia purpurea.

摘要

对海绵动物Zyzzya属的四个不同样本进行详细分析后,得到了9种属于makaluvamine、batzelline和异batzelline/damirone类别的吡咯并咪唑醌。对其他Zyzzya提取物进行的去重复分析未发现更具活性的或其他新化合物。在国立癌症研究所的60细胞系人类肿瘤筛选试验中对这些化合物进行比较测试,结果显示其活性水平各异且具有不同的细胞毒性,这显然与核心环系统中的不饱和水平和取代模式有关。还对拓扑异构酶II介导的DNA裂解进行了进一步研究。吡咯并咪唑醌的还原激活在体外导致DNA损伤,这与半波电位和可逆性参数相关。抗坏血酸盐可消除DNA损伤。采用荧光位移法测量与DNA的嵌入情况;嵌入效率与DNA损伤能力不相关。Makaluvamine H(5)是我们分离得到的化合物中活性最强且具有差异性的,大致与makaluvamines C(体外)和I(体内)相当。从Zyzzya的一个样本以及海绵Latrunculia purpurea中分离出了3,7-二甲基鸟嘌呤。

相似文献

1
Antitumor activity and distribution of pyrroloiminoquinones in the sponge genus Zyzzya.吡咯并咪唑醌类化合物在海绵动物齐氏海绵属中的抗肿瘤活性及分布
Bioorg Med Chem. 2005 Nov 1;13(21):6035-44. doi: 10.1016/j.bmc.2005.06.019.
2
Antimalarial activity of pyrroloiminoquinones from the Australian marine sponge Zyzzya sp.吡咯并[2,3-f]喹啉酮类衍生物的抗疟活性来自澳大利亚海洋海绵 Zyzzya sp.
J Med Chem. 2012 Jun 28;55(12):5851-8. doi: 10.1021/jm3002795. Epub 2012 Jun 20.
3
Makaluvamine N: a new pyrroloiminoquinone from Zyzzya fuliginosa.马卡鲁胺N:一种来自黑紫椰爵床的新型吡咯并亚氨基醌。
J Nat Prod. 1997 Apr;60(4):408-10. doi: 10.1021/np9607262.
4
Another Look at Pyrroloiminoquinone Alkaloids-Perspectives on Their Therapeutic Potential from Known Structures and Semisynthetic Analogues.重新审视吡咯并咪唑醌生物碱——从已知结构和半合成类似物看其治疗潜力
Mar Drugs. 2017 Mar 29;15(4):98. doi: 10.3390/md15040098.
5
Cytotoxic pyrroloiminoquinones from four new species of South African latrunculid sponges.来自四种南非梭子海绵新物种的细胞毒性吡咯并亚氨基醌。
J Nat Prod. 2004 Aug;67(8):1268-76. doi: 10.1021/np034084b.
6
Molecular Networking Reveals Two Distinct Chemotypes in Pyrroloiminoquinone-Producing Tsitsikamma favus Sponges.分子网络揭示了产吡咯并[2,3-f]喹喔啉酮的 Tsitsikamma favus 海绵中的两种不同化学型。
Mar Drugs. 2019 Jan 16;17(1):60. doi: 10.3390/md17010060.
7
Zyzzyanones B-D, dipyrroloquinones from the marine sponge Zyzzya fuliginosa.紫胶醌B-D,来自海洋海绵紫胶漆斑菌的二吡咯醌。
J Nat Prod. 2005 Sep;68(9):1424-7. doi: 10.1021/np050154y.
8
Makaluvamines, marine natural products, are active anti-cancer agents and DNA topo II inhibitors.马卡鲁胺类海洋天然产物是活性抗癌剂和DNA拓扑异构酶II抑制剂。
Anticancer Drug Des. 1993 Oct;8(5):333-47.
9
Current Perspectives on Pyrroloiminoquinones: Distribution, Biosynthesis and Drug Discovery Potential.吡咯并[2,3-f]喹啉醌的研究现状:分布、生物合成及药物研发潜力。
Molecules. 2022 Dec 9;27(24):8724. doi: 10.3390/molecules27248724.
10
Discorhabdins S, T, and U, new cytotoxic pyrroloiminoquinones from a deep-water Caribbean sponge of the genus Batzella.Discorhabdins S、T和U,从加勒比海深水巴泽海绵属海绵中分离出的新型细胞毒性吡咯并亚氨基醌。
J Nat Prod. 2003 Dec;66(12):1615-7. doi: 10.1021/np030292s.

引用本文的文献

1
Current Perspectives on Pyrroloiminoquinones: Distribution, Biosynthesis and Drug Discovery Potential.吡咯并[2,3-f]喹啉醌的研究现状:分布、生物合成及药物研发潜力。
Molecules. 2022 Dec 9;27(24):8724. doi: 10.3390/molecules27248724.
2
Anticancer Activities of Marine-Derived Phenolic Compounds and Their Derivatives.海洋来源的酚类化合物及其衍生物的抗癌活性。
Molecules. 2022 Feb 21;27(4):1449. doi: 10.3390/molecules27041449.
3
Synthetic Makaluvamine Analogs Decrease c-Kit Expression and Are Cytotoxic to Neuroendocrine Tumor Cells.
合成马卡卢瓦明类似物降低 c-Kit 表达并对神经内分泌肿瘤细胞具有细胞毒性。
Molecules. 2020 Oct 26;25(21):4940. doi: 10.3390/molecules25214940.
4
Molecular Networking Reveals Two Distinct Chemotypes in Pyrroloiminoquinone-Producing Tsitsikamma favus Sponges.分子网络揭示了产吡咯并[2,3-f]喹喔啉酮的 Tsitsikamma favus 海绵中的两种不同化学型。
Mar Drugs. 2019 Jan 16;17(1):60. doi: 10.3390/md17010060.
5
Synthesis of Jacaranone-Derived Nitrogenous Cyclohexadienones and Their Antiproliferative and Antiprotozoal Activities.Jacaranone 衍生含氮环己二烯酮的合成及其抗增殖和抗原生动物活性。
Molecules. 2018 Nov 7;23(11):2902. doi: 10.3390/molecules23112902.
6
Another Look at Pyrroloiminoquinone Alkaloids-Perspectives on Their Therapeutic Potential from Known Structures and Semisynthetic Analogues.重新审视吡咯并咪唑醌生物碱——从已知结构和半合成类似物看其治疗潜力
Mar Drugs. 2017 Mar 29;15(4):98. doi: 10.3390/md15040098.
7
Recent advances in isolation, synthesis, and evaluation of bioactivities of bispyrroloquinone alkaloids of marine origin.海洋来源双吡咯并醌生物碱的分离、合成及生物活性评价的最新进展
Chin J Nat Med. 2015 Aug;13(8):561-77. doi: 10.1016/S1875-5364(15)30052-2.
8
Natural product MDM2 inhibitors: anticancer activity and mechanisms of action.天然产物 MDM2 抑制剂:抗癌活性及作用机制。
Curr Med Chem. 2012;19(33):5705-25. doi: 10.2174/092986712803988910.
9
Experimental therapy of ovarian cancer with synthetic makaluvamine analog: in vitro and in vivo anticancer activity and molecular mechanisms of action.用合成马卡鲁瓦明类似物治疗卵巢癌的实验疗法:体外和体内抗癌活性及作用机制。
PLoS One. 2011;6(6):e20729. doi: 10.1371/journal.pone.0020729. Epub 2011 Jun 6.
10
Synthesis of the marine pyrroloiminoquinone alkaloids, discorhabdins.海洋吡咯并[2,1-f][1,4]苯并二氮杂*-5,11-二酮生物碱,discorhabdins 的合成。
Mar Drugs. 2010 Apr 21;8(4):1394-416. doi: 10.3390/md8041394.