Show simple item record

Mutagenicity of aryl propylene and butylene oxides with Salmonella

dc.contributor.authorRosman, L. B.en_US
dc.contributor.authorGaddamidi, V.en_US
dc.contributor.authorSinsheimer, Joseph E.en_US
dc.date.accessioned2006-04-07T19:46:22Z
dc.date.available2006-04-07T19:46:22Z
dc.date.issued1987-11en_US
dc.identifier.citationRosman, L. B., Gaddamidi, V., Sinsheimer, J. E. (1987/11)."Mutagenicity of aryl propylene and butylene oxides with Salmonella." Mutation Research/Genetic Toxicology 189(3): 189-204. <http://hdl.handle.net/2027.42/26518>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B73FB-475NY07-16/2/8fac61af96911807d4c4b79ca2987a8aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26518
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3313034&dopt=citationen_US
dc.description.abstract10 aryl propylene oxides and 6 aryl butylene oxides were synthesized. Dose-mutagenicity relationships were studied for these compounds and for 1,2-epoxybutane, using both the preincubation and plate incorporation Ames tests with Salmonella typhimurium strains TA100 and TA1535. Structure-mutagenicity relationships were further examined by concurrent testing at single doses with the plate incorporation assay in strain TA100. In both series of compounds, mutagenicity showed very weak correlation to chemical reactivity, molar volume and partition values. However, all compounds were mutagenic in at least one system with the propylene oxides being more mutagenic than the corresponding butylene oxide derivatives. The naphthyl derivatives in each series were the most mutagenic.en_US
dc.format.extent891739 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleMutagenicity of aryl propylene and butylene oxides with Salmonellaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCollege of Pharmacy, University of Michigan, Ann Arbor, MI 48109-1065, U.S.A.en_US
dc.contributor.affiliationumCollege of Pharmacy, University of Michigan, Ann Arbor, MI 48109-1065, U.S.A.en_US
dc.contributor.affiliationumCollege of Pharmacy, University of Michigan, Ann Arbor, MI 48109-1065, U.S.A.en_US
dc.identifier.pmid3313034en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26518/1/0000056.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0165-1218(87)90053-Xen_US
dc.identifier.sourceMutation Research/Genetic Toxicologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.