• 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

GERI-BP001化合物,烟曲霉F37酰基辅酶A:胆固醇酰基转移酶的新型抑制剂。I. 生产、分离以及物理化学和生物学特性

GERI-BP001 compounds, new inhibitors of acyl-CoA: cholesterol acyltransferase from Aspergillus fumigatus F37. I. Production, isolation, and physico-chemical and biological properties.

作者信息

Jeong T S, Kim S U, Son K H, Kwon B M, Kim Y K, Choi M U, Bok S H

机构信息

Bioproducts Research Group, Korea Research Institute of Bioscience & Biotechnology, KIST, Taejon.

出版信息

J Antibiot (Tokyo). 1995 Aug;48(8):751-6. doi: 10.7164/antibiotics.48.751.

DOI:10.7164/antibiotics.48.751
PMID:7592016
Abstract

GERI-BP001 compounds, new inhibitors of acyl-CoA:cholesterol acyltransferase (ACAT), were isolated from a culture broth of Aspergillus fumigatus F37 by acetone extraction, EtOAc extraction, SiO2 column chromatography, and reverse phase HPLC. GERI-BP001 M, A, and B inhibit ACAT activity in an enzyme assay system using rat liver microsomes by 50% at concentrations of 42, 94, and 40 microM, respectively.

摘要

GERI - BP001化合物是酰基辅酶A:胆固醇酰基转移酶(ACAT)的新型抑制剂,通过丙酮萃取、乙酸乙酯萃取、硅胶柱色谱和反相高效液相色谱从烟曲霉F37的培养液中分离得到。在使用大鼠肝微粒体的酶分析系统中,GERI - BP001 M、A和B分别在浓度为42、94和40微摩尔时抑制ACAT活性达50%。

相似文献

1
GERI-BP001 compounds, new inhibitors of acyl-CoA: cholesterol acyltransferase from Aspergillus fumigatus F37. I. Production, isolation, and physico-chemical and biological properties.GERI-BP001化合物,烟曲霉F37酰基辅酶A:胆固醇酰基转移酶的新型抑制剂。I. 生产、分离以及物理化学和生物学特性
J Antibiot (Tokyo). 1995 Aug;48(8):751-6. doi: 10.7164/antibiotics.48.751.
2
Pyripyropenes, novel inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus. I. Production, isolation, and biological properties.烟曲霉产生的新型酰基辅酶A:胆固醇酰基转移酶抑制剂——吡啶并吡喃类化合物。I. 产生、分离及生物学特性
J Antibiot (Tokyo). 1994 Feb;47(2):148-53. doi: 10.7164/antibiotics.47.148.
3
GERI-BP002-A, novel inhibitor of acyl-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus F93.GERI-BP002-A,烟曲霉F93产生的新型酰基辅酶A:胆固醇酰基转移酶抑制剂。
J Antibiot (Tokyo). 1996 Jan;49(1):31-6. doi: 10.7164/antibiotics.49.31.
4
Pyripyropenes, Novel ACAT inhibitors produced by Aspergillus fumigatus. III. Structure elucidation of pyripyropenes E to L.焦曲霉产生的新型乙酰辅酶A酰基转移酶(ACAT)抑制剂——焦曲霉烯类。III. 焦曲霉烯类E至L的结构解析
J Antibiot (Tokyo). 1995 Jun;48(6):495-503. doi: 10.7164/antibiotics.48.495.
5
Pyripyropenes, novel ACAT inhibitors produced by Aspergillus fumigatus. IV. Structure elucidation of pyripyropenes M to R.烟曲霉产生的新型ACAT抑制剂——吡啶并吡咯烯类化合物。IV. 吡啶并吡咯烯类化合物M至R的结构解析
J Antibiot (Tokyo). 1996 Mar;49(3):292-8. doi: 10.7164/antibiotics.49.292.
6
Pyripyropenes, novel inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus. II. Structure elucidation of pyripyropenes A, B, C and D.烟曲霉产生的新型酰基辅酶A:胆固醇酰基转移酶抑制剂——吡喃并吡咯类化合物。II. 吡喃并吡咯类化合物A、B、C和D的结构解析
J Antibiot (Tokyo). 1994 Feb;47(2):154-62. doi: 10.7164/antibiotics.47.154.
7
Penicillium griseofulvum F1959, high-production strain of pyripyropene a, specific inhibitor of acyl-CoA: cholesterol acyltransferase 2.灰黄青霉F1959,吡喃并吡咯菌素A的高产菌株,酰基辅酶A:胆固醇酰基转移酶2的特异性抑制剂。
J Microbiol Biotechnol. 2008 Oct;18(10):1663-5.
8
Purpactins, new inhibitors of acyl-CoA:cholesterol acyltransferase produced by Penicillium purpurogenum. I. Production, isolation and physico-chemical and biological properties.紫青霉素,由产紫青霉产生的新型酰基辅酶A:胆固醇酰基转移酶抑制剂。I. 生产、分离以及物理化学和生物学性质
J Antibiot (Tokyo). 1991 Feb;44(2):136-43. doi: 10.7164/antibiotics.44.136.
9
Pyripyropenes, highly potent inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus.烟曲霉素,由烟曲霉产生的酰基辅酶A:胆固醇酰基转移酶的高效抑制剂。
J Antibiot (Tokyo). 1993 Jul;46(7):1168-9. doi: 10.7164/antibiotics.46.1168.
10
Isolation of Acyl-CoA:cholesterol acyltransferase inhibitor from Persicaria vulgaris.
Planta Med. 2002 Sep;68(9):845-7. doi: 10.1055/s-2002-34395.

引用本文的文献

1
from Pathogenic Fungus to Unexplored Natural Treasure: Changing the Concept.从致病真菌到未被发掘的天然宝藏:转变观念。
J Microbiol Biotechnol. 2025 Mar 11;35:e2411082. doi: 10.4014/jmb.2411.11082.
2
Old tricks, new dogs: organocatalytic dienamine activation of α,β-unsaturated aldehydes.老方法,新应用:α,β-不饱和醛的有机催化烯胺活化
Chem Soc Rev. 2016 Dec 21;45(24):6812-6832. doi: 10.1039/c6cs00438e. Epub 2016 Nov 2.
3
Reconstitution of a fungal meroterpenoid biosynthesis reveals the involvement of a novel family of terpene cyclases.
真菌混合萜类生物合成的重建揭示了一类新型萜烯环化酶的参与。
Nat Chem. 2010 Oct;2(10):858-64. doi: 10.1038/nchem.764. Epub 2010 Aug 1.