Synthesis and structure reassignment of mercaptohistidines of marine origin. Syntheses of L-ovothiols A and C
- 1 September 1987
- journal article
- letter
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (19), 4420-4421
- https://doi.org/10.1021/jo00228a060
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- New synthesis of 4- and 5-imidazolethiolsThe Journal of Organic Chemistry, 1987
- Ovothiols, a family of redox-active mercaptohistidine compounds from marine invertebrate eggsBiochemistry, 1987
- Ovothiol: a novel thiohistidine compound from sea urchin eggs that confers NAD(P)H-O2 oxidoreductase activity on ovoperoxidase.Journal of Biological Chemistry, 1986
- Isolation and distribution of 1-methyl-5-thiol-l-histidine disulphide and a related metabolite in eggs from echinodermsComparative Biochemistry and Physiology Part B: Comparative Biochemistry, 1984
- Isolation and characterization of adenochrome, a unique iron(III)-binding peptide from Octopus vulgarisJournal of the Chemical Society, Perkin Transactions 1, 1979