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dc.contributor.authorKamau, FN
dc.contributor.authorKibwage, IO
dc.contributor.authorMuriuki, G
dc.contributor.authorGuantai, AN
dc.contributor.authorChepkwony, H
dc.contributor.authorHoogmartens, J
dc.contributor.authorRoets, E.
dc.contributor.authorBusson, R
dc.date.accessioned2013-02-20T10:13:22Z
dc.date.issued2006
dc.identifier.citationEast and Central African Journal ofPhannaceutical Sciences Vol. 9 (2006) 52-57en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/10433
dc.description.abstractThree steroidal indoxyls, 3-oxo-16,17-seco-16;.nor-l,4-androstadien-15-(7'-methoxy-2-indoxyliden)17-oic acid, 1-(2'-indoxyliden)-2-nor-l,2-secocholestan-3~ oic acid and 1-(5'- chloro-2-indoxyliden)-2-nor-l,2-secocholestan-3-oic acid were synthesized and screened for anti-inflammatory activity. Their pK. values were also determined using a solubility method. The first compound, 3-oxo-16,17- seco-16-nor-l ,4-androstadien-15-(7' -methoxy-2-indoxyliden) 17 -oic acid, had an EDso value of 15.3 mg/kg and a pK. of 7.09. The cholestane derivative, 1-(2'-indoxyliden)-2-nor-l,2-secocholestan-3-oic acid, and its chloro analogue 1-(5'-chloro-2-indoxyliden)-2-nor-l,2-secocholestan-3-oic acid had EDso values of 16.2 and 22.8 mg/kg, while their pK. values were 6.56 and 7.07, respectively, suggesting that these compounds are relatively weak acids.en
dc.language.isoenen
dc.subjectSteroidal indoxyls,en
dc.subjectPka values,en
dc.subjectAnti-inflammatoryen
dc.titleSteroidal Indoxyls: Evaluation of Pk, values and anti-inflammatory activityen
dc.title.alternativeEvaluation of Pk, values and anti-inflammatory activityen
dc.typeArticleen
local.publisherDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Nairobien
local.publisher'Department of Pharmacology and Pharmacognosy, School of Pharmacy, University of Nairobien
local.publisherNational Quality Control Laboratory,en
local.publisherKatholieke Universiteit Leuven, Faculteit Farmaceutische Wetenschappen, Van Evenstraaten


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