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Carboxy Alkyl Cysteines

dc.contributor.authorSmith, John Walter
dc.date.accessioned2009-04-14T22:03:26Z
dc.date.accessioned2022-10-17T21:07:35Z
dc.date.available2009-04-14T22:03:26Z
dc.date.available2022-10-17T21:07:35Z
dc.date.copyright1969
dc.date.issued1969
dc.description.abstractA. S-Alkyl substituted cysteines and their sulphoxides (I) Structure These compounds comprise a large number of cysteine derivatives in which the thiol hydrogen is replaced by various aliphatic residues. The basic structure is R - S - CH2-CH.(NH2).COOH where R represents the aliphatic residue, which may range in size from methyl to 2-carboxy-1,1-dimethylethyl. The corresponding sulphoxides of the structurally simpler compound are also known to occur naturally, an example of these being S-methyl-L-cysteine.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/22066
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.rights.holderAll rights, except those explicitly waived, are held by the Authoren_NZ
dc.rights.licenseAuthor Retains Copyrighten_NZ
dc.rights.urihttps://www.wgtn.ac.nz/library/about-us/policies-and-strategies/copyright-for-the-researcharchive
dc.subjectBiochemistryen_NZ
dc.titleCarboxy Alkyl Cysteinesen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineBiochemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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