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172 related items for PubMed ID: 884667
1. Covalent interaction of dehydroretronecine, a carcinogenic metabolite of the pyrrolizidine alkaloid monocrotaline, with cysteine and glutathione. Robertson KA, Seymour JL, Hsia MT, Allen JR. Cancer Res; 1977 Sep; 37(9):3141-4. PubMed ID: 884667 [Abstract] [Full Text] [Related]
2. Alkylation of N2 in deoxyguanosine by dehydroretronecine, a carcinogenic metabolite of the pyrrolizidine alkaloid monocrotaline. Robertson KA. Cancer Res; 1982 Jan; 42(1):8-14. PubMed ID: 6797726 [Abstract] [Full Text] [Related]
3. Human liver microsomal reduction of pyrrolizidine alkaloid N-oxides to form the corresponding carcinogenic parent alkaloid. Wang YP, Yan J, Fu PP, Chou MW. Toxicol Lett; 2005 Mar 15; 155(3):411-20. PubMed ID: 15649625 [Abstract] [Full Text] [Related]
4. Identity of a biliary metabolite formed from monocrotaline in isolated, perfused rat liver. Mattocks AR, Croswell S, Jukes R, Huxtable RJ. Toxicon; 1991 Mar 15; 29(4-5):409-15. PubMed ID: 1907409 [Abstract] [Full Text] [Related]
5. Alkylation by dehydroretronecine, a cytotoxic metabolite of some pyrrolizidine alkaloids: an in vitro test. Mattocks AR, Bird I. Toxicol Lett; 1983 Apr 15; 16(1-2):1-8. PubMed ID: 6836605 [Abstract] [Full Text] [Related]
6. Metabolic activation of pyrrolizidine alkaloids by human, rat and avocado microsomes. Couet CE, Hopley J, Hanley AB. Toxicon; 1996 Sep 15; 34(9):1058-61. PubMed ID: 8896199 [Abstract] [Full Text] [Related]
7. A new pyrrolizidine alkaloid metabolite, 19-hydroxysenecionine isolated from mouse hepatic microsomes in vitro. Eastman DF, Segall HJ. Drug Metab Dispos; 1982 Sep 15; 10(6):696-9. PubMed ID: 6130926 [Abstract] [Full Text] [Related]
8. Binding of tritiated dehydroretronecine to macromolecules. Hsu IC, Robertson KA, Shumaker RC, Allen JR. Res Commun Chem Pathol Pharmacol; 1975 May 15; 11(1):99-106. PubMed ID: 239444 [Abstract] [Full Text] [Related]
9. Effects of glutathione and cysteine on pyrrolizidine alkaloid-induced hepatotoxicity and DNA adduct formation in rat primary hepatocytes. He X, Xia Q, Shi Q, Fu PP. J Environ Sci Health C Toxicol Carcinog; 2020 May 15; 38(2):109-123. PubMed ID: 32500832 [Abstract] [Full Text] [Related]
11. Activation of monocrotaline, fulvine and their derivatives to toxic pyrroles by some thiols. Juneja TR, Gupta RL, Samanta S. Toxicol Lett; 1984 May 15; 21(2):185-9. PubMed ID: 6426098 [Abstract] [Full Text] [Related]
12. Isolation and identification of a pyrrolic glutathione conjugate metabolite of the pyrrolizidine alkaloid monocrotaline. Lamé MW, Morin D, Jones AD, Segall HJ, Wilson DW. Toxicol Lett; 1990 May 15; 51(3):321-9. PubMed ID: 2111054 [Abstract] [Full Text] [Related]
13. Formation of DHP-derived DNA adducts from metabolic activation of the prototype heliotridine-type pyrrolizidine alkaloid, heliotrine. Xia Q, Yan J, Chou MW, Fu PP. Toxicol Lett; 2008 May 05; 178(2):77-82. PubMed ID: 18395999 [Abstract] [Full Text] [Related]
14. 7-Glutathione-pyrrole and 7-cysteine-pyrrole are potential carcinogenic metabolites of pyrrolizidine alkaloids. He X, Xia Q, Fu PP. J Environ Sci Health C Environ Carcinog Ecotoxicol Rev; 2017 Apr 03; 35(2):69-83. PubMed ID: 28418776 [Abstract] [Full Text] [Related]
16. 7-cysteine-pyrrole conjugate: A new potential DNA reactive metabolite of pyrrolizidine alkaloids. He X, Xia Q, Ma L, Fu PP. J Environ Sci Health C Environ Carcinog Ecotoxicol Rev; 2016 Apr 03; 34(1):57-76. PubMed ID: 26761716 [Abstract] [Full Text] [Related]