• 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

库拉索菌素A和B,由拟青霉属FO-3684菌株产生的新型蛋白质法尼基转移酶抑制剂。II. 结构解析与全合成。

Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. II. Structure elucidation and total synthesis.

作者信息

Uchida R, Shiomi K, Sunazuka T, Inokoshi J, Nishizawa A, Hirose T, Tanaka H, Iwai Y, Omura S

机构信息

Research Center for Biological Function, Kitasato Institute, Tokyo, Japan.

出版信息

J Antibiot (Tokyo). 1996 Sep;49(9):886-9. doi: 10.7164/antibiotics.49.886.

DOI:10.7164/antibiotics.49.886
PMID:8931722
Abstract

The structures of new protein farnesyltransferase inhibitors, kurasoins A and B, were elucidated by NMR study. Kurasoins A and B are acyloin compounds having in common a 3-hydroxy-1-phenyl-2-butanone moiety, to which p-hydroxyphenyl and 3-indolyl moieties respectively, are connected at C-4. The structures were confirmed by total synthesis.

摘要

通过核磁共振研究阐明了新型蛋白质法尼基转移酶抑制剂库拉索因A和B的结构。库拉索因A和B是偶姻化合物,它们共同具有一个3-羟基-1-苯基-2-丁酮部分,在C-4位分别连接有对羟基苯基和3-吲哚基部分。通过全合成确认了其结构。

相似文献

1
Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. II. Structure elucidation and total synthesis.库拉索菌素A和B,由拟青霉属FO-3684菌株产生的新型蛋白质法尼基转移酶抑制剂。II. 结构解析与全合成。
J Antibiot (Tokyo). 1996 Sep;49(9):886-9. doi: 10.7164/antibiotics.49.886.
2
Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. I. Producing strain, fermentation, isolation, and biological activities.库拉索菌素A和B,由拟青霉属菌株FO-3684产生的新型蛋白质法尼基转移酶抑制剂。I. 产生菌株、发酵、分离及生物活性。
J Antibiot (Tokyo). 1996 Sep;49(9):932-4. doi: 10.7164/antibiotics.49.932.
3
Syntheses and absolute structures of novel protein farnesyltransferase inhibitors, kurasoins A and B.新型蛋白质法尼基转移酶抑制剂库拉索因A和B的合成及绝对结构
J Antibiot (Tokyo). 1997 May;50(5):453-5. doi: 10.7164/antibiotics.50.453.
4
Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. I. Producing strain, fermentation, isolation, and biological activities.安曲霉素A-C,由青霉菌FO-3929产生的新型蛋白法尼基转移酶抑制剂。I. 产生菌、发酵、分离及生物活性。
J Antibiot (Tokyo). 1996 May;49(5):414-7. doi: 10.7164/antibiotics.49.414.
5
Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. II. Structure elucidation and biosynthesis.安曲汀A-C,由青霉菌FO-3929产生的新型蛋白质法尼基转移酶抑制剂。II. 结构解析与生物合成。
J Antibiot (Tokyo). 1996 May;49(5):418-24. doi: 10.7164/antibiotics.49.418.
6
Andrastin D, novel protein farnesyltransferase inhibitor produced by Penicillium sp. FO-3929.
J Antibiot (Tokyo). 1996 Dec;49(12):1278-80. doi: 10.7164/antibiotics.49.1278.
7
Benzimidazolones and indoles as non-thiol farnesyltransferase inhibitors based on tipifarnib scaffold: synthesis and activity.基于替匹法尼骨架的苯并咪唑酮类和吲哚类化合物作为非硫醇法尼基转移酶抑制剂:合成与活性
Bioorg Med Chem Lett. 2005 Jun 2;15(11):2918-22. doi: 10.1016/j.bmcl.2005.03.049. Epub 2005 Apr 21.
8
Synthesis and conformational analysis of peptide inhibitors of farnesyltransferase.法尼基转移酶肽抑制剂的合成与构象分析
Bioorg Med Chem. 1997 Jan;5(1):115-24. doi: 10.1016/s0968-0896(96)00210-6.
9
Novel conformationally extended naphthalene-based inhibitors of farnesyltransferase.
J Med Chem. 1997 Jun 6;40(12):1763-7. doi: 10.1021/jm9701177.
10
Farnesyltransferase inhibitors: a new class of cancer chemotherapeutics.法尼基转移酶抑制剂:一类新型癌症化疗药物。
Biochem Soc Trans. 1996 Aug;24(3):688-92. doi: 10.1042/bst0240688.

引用本文的文献

1
Visible-light-induced nickel-catalyzed α-hydroxytrifluoroethylation of alkyl carboxylic acids: Access to trifluoromethyl alkyl acyloins.可见光诱导的镍催化烷基羧酸的α-羟基三氟乙基化反应:通向三氟甲基烷基偶姻的途径。
Beilstein J Org Chem. 2023 Sep 11;19:1372-1378. doi: 10.3762/bjoc.19.98. eCollection 2023.
2
CsCO-Promoted reaction of tertiary bromopropargylic alcohols and phenols in DMF: a novel approach to α-phenoxyketones.碳酸铯促进叔溴代炔丙醇与酚在N,N-二甲基甲酰胺中的反应:一种合成α-苯氧基酮的新方法。
Beilstein J Org Chem. 2022 Apr 12;18:420-428. doi: 10.3762/bjoc.18.44. eCollection 2022.
3
Secondary Metabolites and Their Bioactivities Produced by .
海洋真菌. 产生的次生代谢产物及其生物活性
Molecules. 2020 Nov 1;25(21):5077. doi: 10.3390/molecules25215077.
4
Discovery and total synthesis of a new estrogen receptor heterodimerizing actinopolymorphol A from Actinopolymorpha rutilus.从 Actinopolymorpha rutilus 中发现并全合成新型雌激素受体异二聚化化合物 actinopolymorphol A。
Org Lett. 2010 Aug 6;12(15):3525-7. doi: 10.1021/ol1013526.