• 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

从新喀里多尼亚深海海洋海绵Orina Sp.中提取的其他溴化双吲哚和三吲哚生物碱

Further brominated bis- and tris-indole alkaloids from the deep-water New Caledonian marine sponge Orina Sp.

作者信息

Bifulco G, Bruno I, Riccio R, Lavayre J, Bourdy G

机构信息

Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli Ferderico II, Italy.

出版信息

J Nat Prod. 1995 Aug;58(8):1254-60. doi: 10.1021/np50122a017.

DOI:10.1021/np50122a017
PMID:7595591
Abstract

Two tris-indole alkaloids, (+/-) gelliusines A and B [1], have been isolated for the first time from a marine source, the New Caledonian sponge, Orina sp. (or Gellius sp.), along with five further indole constituents [2-6]. Compound 6 has been identified as 2,2-bis-(6'-bromo-3'-indolyl(-ethylamine, previously isolated from the tunicate Didemnum candidum, but the remaining four indoles [2-5] are novel compounds. These showed anti-serotonin activity and a strong affinity for somatostatin and neuropeptide Y receptors in receptor-binding assays.

摘要

首次从海洋来源新喀里多尼亚海绵Orina sp.(或Gellius sp.)中分离出两种三吲哚生物碱,即(±)盖利辛A和B [1],同时,同时还分离出另外五种吲哚成分[2-6]。化合物6已被鉴定为2,2-双-(6'-溴-3'-吲哚基)乙胺,该化合物先前已从被囊动物白色皮海鞘中分离得到,但其余四种吲哚[2-5]是新化合物。在受体结合试验中,这些化合物表现出抗血清素活性,并对生长抑素和神经肽Y受体具有很强的亲和力。

相似文献

1
Further brominated bis- and tris-indole alkaloids from the deep-water New Caledonian marine sponge Orina Sp.从新喀里多尼亚深海海洋海绵Orina Sp.中提取的其他溴化双吲哚和三吲哚生物碱
J Nat Prod. 1995 Aug;58(8):1254-60. doi: 10.1021/np50122a017.
2
(+/-)-Gelliusines A and B, two diastereomeric brominated tris-indole alkaloids from a deep water new caledonian marine sponge (Gellius or Orina sp.).(±)-盖利乌辛A和B,两种非对映体溴化三吲哚生物碱,从新喀里多尼亚深水海洋海绵(盖利乌斯属或奥里纳属海绵)中提取得到。
J Nat Prod. 1994 Sep;57(9):1294-9. doi: 10.1021/np50111a020.
3
Hamacanthins A and B, new antifungal bis indole alkaloids from the deep-water marine sponge, Hamacantha sp.哈马坎亭A和B,源自深水海洋海绵哈马坎塔属(Hamacantha sp.)的新型抗真菌双吲哚生物碱
J Nat Prod. 1994 Oct;57(10):1437-41. doi: 10.1021/np50112a014.
4
Four new dimeric peptide alkaloids, anchinopeptolides B-D, and cycloanchinopeptolide C, congeners of anchinopeptolide A, from the Mediterranean marine sponge Anchinoe tenacior.从地中海海洋海绵坚韧锚海绵(Anchinoe tenacior)中分离出四种新的二聚体肽生物碱,即锚肽内酯B - D和环锚肽内酯C,它们是锚肽内酯A的同系物。
J Nat Prod. 1994 Sep;57(9):1227-33. doi: 10.1021/np50111a006.
5
Comparison of fascaplysin and related alkaloids: a study of structures, cytotoxicities, and sources.法斯卡普利辛及相关生物碱的比较:结构、细胞毒性及来源的研究
J Nat Prod. 2004 May;67(5):783-92. doi: 10.1021/np049935+.
6
Brominated indole alkaloids from the marine tunicate Pseudodistoma arborescens.来自海洋被囊动物树状拟双体海鞘的溴化吲哚生物碱。
J Nat Prod. 1993 Jan;56(1):99-104. doi: 10.1021/np50091a014.
7
Bis(indole) alkaloids as sortase A inhibitors from the sponge Spongosorites sp.来自海绵Spongosorites sp.的双(吲哚)生物碱作为分选酶A抑制剂
Bioorg Med Chem Lett. 2005 Nov 15;15(22):4927-31. doi: 10.1016/j.bmcl.2005.08.021.
8
Two new alkaloids from Xestospongia sp., a New Caledonian sponge.
J Nat Prod. 1992 Oct;55(10):1505-8. doi: 10.1021/np50088a017.
9
1,2-bis(1H-indol-3-yl)ethane-1,2-dione, an indole alkaloid from the marine sponge Smenospongia sp.1,2-双(1H-吲哚-3-基)乙烷-1,2-二酮,一种从海洋海绵Smenospongia sp.中提取的吲哚生物碱。
J Nat Prod. 2002 Apr;65(4):595-7. doi: 10.1021/np010347v.
10
Novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella verrucosa.来自地中海海绵疣轴海绵的新型生物活性溴吡咯生物碱。
Bioorg Med Chem. 2006 Jan 1;14(1):17-24. doi: 10.1016/j.bmc.2005.07.057. Epub 2005 Sep 16.

引用本文的文献

1
Green Synthesis of Primary Aniline-Based Indolylmethanes via One-Pot Aza-Friedel-Crafts Reaction Catalyzed by Brønsted Acidic Ionic Liquid in Aqueous Media.在水介质中通过布朗斯台德酸性离子液体催化的一锅法氮杂傅-克反应实现基于苯胺的吲哚甲烷的绿色合成。
ACS Omega. 2025 Aug 2;10(31):34951-34963. doi: 10.1021/acsomega.5c04294. eCollection 2025 Aug 12.
2
Short Total Synthesis of (+)-Colletotryptins B-D and Mucronatin B Derivative.(+)- 炭疽菌素 B-D 和刺桐碱 B 衍生物的短全合成。
J Org Chem. 2024 Jun 21;89(12):8620-8631. doi: 10.1021/acs.joc.4c00552. Epub 2024 May 29.
3
Advances in the total synthesis of bis- and tris-indole alkaloids containing N-heterocyclic linker moieties.
含 N-杂环连接基团的双吲哚和三吲哚生物碱的全合成进展。
Nat Prod Rep. 2024 Aug 14;41(8):1264-1293. doi: 10.1039/d4np00012a.
4
Relevant Developments in the Use of Three-Component Reactions for the Total Synthesis of Natural Products. The last 15 Years.用于天然产物全合成的三组分反应的相关进展。过去15年。
ChemistryOpen. 2024 May;13(5):e202300306. doi: 10.1002/open.202300306. Epub 2024 Apr 22.
5
LiOBu-promoted synthesis of bis(3-indolyl)methanes by the alkylation of indoles with alcohols under air.在空气中,通过吲哚与醇的烷基化反应,由丁基锂促进合成双(3-吲哚基)甲烷。
RSC Adv. 2024 Jan 11;14(4):2341-2345. doi: 10.1039/d3ra07115d. eCollection 2024 Jan 10.
6
Marine-derived fungi as a source of bioactive indole alkaloids with diversified structures.海洋来源真菌作为具有多样结构的生物活性吲哚生物碱的来源。
Mar Life Sci Technol. 2020 Nov 24;3(1):44-61. doi: 10.1007/s42995-020-00072-w. eCollection 2021 Feb.
7
Organocatalytic enantioselective S1-type dehydrative nucleophilic substitution: access to bis(indolyl)methanes bearing quaternary carbon stereocenters.有机催化对映选择性S1型脱水亲核取代反应:构建含季碳立体中心的双(吲哚基)甲烷类化合物
Chem Sci. 2021 Nov 23;13(1):170-177. doi: 10.1039/d1sc05174a. eCollection 2021 Dec 22.
8
Neural versus alternative integrative systems: molecular insights into origins of neurotransmitters.神经与替代整合系统:神经递质起源的分子见解。
Philos Trans R Soc Lond B Biol Sci. 2021 Mar 29;376(1821):20190762. doi: 10.1098/rstb.2019.0762. Epub 2021 Feb 8.
9
New Antimalarial and Antimicrobial Tryptamine Derivatives from the Marine Sponge .新型抗疟和抗微生物色胺衍生物来自海洋海绵。
Mar Drugs. 2019 Mar 15;17(3):167. doi: 10.3390/md17030167.
10
Marine Alkaloid 2,2-Bis(6-bromo-3-indolyl) Ethylamine and Its Synthetic Derivatives Inhibit Microbial Biofilms Formation and Disaggregate Developed Biofilms.海洋生物碱2,2-双(6-溴-3-吲哚基)乙胺及其合成衍生物抑制微生物生物膜形成并分解已形成的生物膜。
Microorganisms. 2019 Jan 23;7(2):28. doi: 10.3390/microorganisms7020028.