doi: 10.7164/antibiotics.41.875.
Novel cholecystokinin antagonists from Aspergillus alliaceus. I. Fermentation, isolation, and biological properties
Affiliations
- PMID: 3417561
- DOI: 10.7164/antibiotics.41.875
Item in Clipboard
Novel cholecystokinin antagonists from Aspergillus alliaceus. I. Fermentation, isolation, and biological properties
J Antibiot (Tokyo).
1988 Jul.
Free article
Abstract
The discovery and biological properties of four novel cholecystokinin antagonists produced by Aspergillus alliaceus is described. One of these was seven times more potent than the previously reported asperlicin.
Similar articles
-
Asperlicin, a novel non-peptidal cholecystokinin antagonist from Aspergillus alliaceus. Fermentation, isolation and biological properties.J Antibiot (Tokyo). 1985 Dec;38(12):1633-7. doi: 10.7164/antibiotics.38.1633. J Antibiot (Tokyo). 1985. PMID: 3005212
-
On the biosynthesis of asperlicin and the directed biosynthesis of analogs in Aspergillus alliaceus.J Antibiot (Tokyo). 1988 Jul;41(7):882-91. doi: 10.7164/antibiotics.41.882. J Antibiot (Tokyo). 1988. PMID: 3417563
-
A potent nonpeptide cholecystokinin antagonist selective for peripheral tissues isolated from Aspergillus alliaceus.Science. 1985 Oct 11;230(4722):177-9. doi: 10.1126/science.2994227. Science. 1985. PMID: 2994227
-
[Cholecystokinin and its antagonists: effects on digestive motility].Gastroenterol Clin Biol. 1991;15(10):744-57. Gastroenterol Clin Biol. 1991. PMID: 1816015 Review. French. No abstract available.
-
[Cholecystokinin antagonists: anxiolytic drugs of the future].Pathol Biol (Paris). 1992 Mar;40(3):215-7. Pathol Biol (Paris). 1992. PMID: 1608663 Review. French. No abstract available.
Cited by
-
Short pathways to complexity generation: fungal peptidyl alkaloid multicyclic scaffolds from anthranilate building blocks.ACS Chem Biol. 2013 Jul 19;8(7):1366-82. doi: 10.1021/cb4001684. Epub 2013 Jun 4. ACS Chem Biol. 2013. PMID: 23659680 Free PMC article. Review.
-
Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.Biochemistry. 2010 Oct 5;49(39):8564-76. doi: 10.1021/bi1012029. Epub 2010 Sep 8. Biochemistry. 2010. PMID: 20804163 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
