New lysine chromogenic substrates for trypsin

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dc.contributor.authorSomorin, O.
dc.contributor.authorOkiei, W.O.
dc.contributor.authorEmokpae, T.
dc.contributor.authorOgunlesi, M.
dc.date.accessioned2019-09-03T12:47:21Z
dc.date.available2019-09-03T12:47:21Z
dc.date.issued1987
dc.descriptionStaff publicationsen_US
dc.description.abstractEight new direct chromogenic lysine substrates, namely N α-benzyloxycarbonyl-l-lysine 3, 5-dinitroanilide hydrochloride (l-ZLDA· Hcl), N α-benzyloxycarbonyl-l-lysine 3-nitroanilide hydrochloride (l-ZLNA· HCl), N α-benzyloxycarbonyl-l-lysine 3-nitro-5-bromoanilide hydrochloride (l-ZLNBA· HCl), N α-benzyloxycarbonyl-l-lysine 3-nitro-5-chloroanilide hydrochloride (l-ZLNCA· HCl), N α-benzyloxycarbonyl-l-lysine 3-nitro-5-fluoroanilide hyrochloride (l-ZLNFA· HCl), N α-benzyloxycarbonyl-l-lysine 3-nitro-5-iodoanilide hydrochloride (l-ZLNIA· HCl), N α-benzyloxycarbonyl-l-lysine 3-nitro-5-(methylsulphonyl) anilide hydrochloride (l-ZLNMA· HCl) and N α-benzyloxycarbonyl-l-lysine 3-nitro-5-(trifluoromethyl) anilide hydrochloride (l-ZLNTA· HCl) were synthesized by the direct condensation of N α-benzyloxycarbonyl, N ϵ-t-butyloxycarbonyl-l-lysine and 3-nitro-5X-substituted aniline,(X= F, Cl, Br, I, H, NO 2, CF 3 or SO 2 CH 3en_US
dc.identifier.citationSomorin, O., Okiei, W., Emokpae, T., and Ogunlesi, M. (1987). New lysine chromogenic substrates for trypsin. International Journal of Biological Macromolecules, 9(1), 27-31.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/5078
dc.language.isoenen_US
dc.publisherElsevier Scienceen_US
dc.relation.ispartofseriesInternational Journal of Biological Macromolecules;Vol.9(1)
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistryen_US
dc.subjectsynthesisen_US
dc.subjectlysine substratesen_US
dc.titleNew lysine chromogenic substrates for trypsinen_US
dc.typeArticleen_US
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