Adetunji J. Aladesanmi
Obafemi Awolowo University
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Featured researches published by Adetunji J. Aladesanmi.
Phytochemistry | 1994
Johannes Reisch; Adeleke Clement Adebajo; Vijaya Kumar; Adetunji J. Aladesanmi
Abstract The non-cyclized possible biogenetic precursors of girinimbine and mahanimbine, 2-hydroxyl-3-methyl-1-(3-methyl-2-butenyl)carbazole (girinimbilol) and 2-hydroxyl-3-methyl-1-(3,7-dimethyl-2,6-octadienyl)carbazole (mahanimbilol) have been isolated from the stem bark of Murraya koenigii. The structures were established by cyclization to dihydrogirinimbine and a new bicyclocarbazole, bicyclomahanimbiline, respectively.
Phytochemistry | 1988
Adetunji J. Aladesanmi; Clement Oladapo Adewunmi; Charles J. Kelley; John D. Leary; Ted A. Bischoff; Xiaolin Zhang; John K. Snyder
Abstract A new, homoerythrina-derived alkaloid with molluscicidal activity, lenticellarine, was isolated from the leaves of Dysoxylum lenticellare and its structure was determined by spectroscopic methods.
Phytochemistry | 1996
Kan He; Barbara N. Timmermann; Adetunji J. Aladesanmi; Lu Zeng
Abstract A novel biflavonoid, robustaflavone 4′,7″-dimethyl ether, has been isolated from the leaves of Dysoxylum lenticellare , in addition to two known compounds, isoginkgetin and bilobetin. Their structures were established by spectroscopic data and chemical modification.
Tetrahedron | 1988
Adetunji J. Aladesanmi
Abstract A total of nine compounds have been isolated from the stem of Dysoxylum lenticellare Gillespie (Meliaceae). They are the five homoerythrina-type alkaloids ( 1 , 2 , 6 , 7 , 9 ), of which 1 and 2 are new. Three diterpenes ( 3 - 5 ) while ( 3 ) is a new compound, compound ( 8 ) is well known. The nine compounds were characterized by the spectroscopic analysis.
Phytochemistry | 1994
Adetunji J. Aladesanmi; Joseph J. Hoffmann
Abstract 2-α-Methoxycomosivine and two presumed homoerythrina-derived alkaloids, 2α-methoxylenticellarine and 2α-hydroxylenticellarine, have been isolated from the stem of Dysoxylum lenticellare . The three alkaloids have been identified by comparison of their spectroscopic properties.
Journal of Diabetes | 2013
Adeleke Clement Adebajo; Marcus Durojaye Ayoola; Samuel Akintunde Odediran; Adetunji J. Aladesanmi; Thomas J. Schmidt; Eugene Joseph Verspohl
The insulinotropic activity of the combined root and stem of Gongronema latifolium (Asclepiadaceae) was evaluated to justify its African ethnomedicinal use in the management of diabetes.
Journal of Diabetes | 2013
Adeleke Clement Adebajo; Ayoola; Samuel Akintunde Odediran; Adetunji J. Aladesanmi; Thomas J. Schmidt; Eugene Joseph Verspohl
The insulinotropic activity of the combined root and stem of Gongronema latifolium (Asclepiadaceae) was evaluated to justify its African ethnomedicinal use in the management of diabetes.
Journal of The Chemical Society, Chemical Communications | 1985
Kay D. Onan; Charles J. Kelley; Chamnan Patarapanich; John D. Leary; Adetunji J. Aladesanmi
Spectroscopic and X-ray diffraction analyses have established the structure and stereochemistry of ferrubietolide, a new bis-diterpene isolated from Dysoxylum Ienticellare, which apparently arises as the result of a Diels–Alder condensation of two dissimilar diterpenes.
Journal of Herbs, Spices & Medicinal Plants | 2013
Adeleke Clement Adebajo; Samuel Akintunde Odediran; Chiaka M. Nneji; Ezekiel O. Iwalewa; G.M. Rukunga; Adetunji J. Aladesanmi; J.W. Gathirwa; Olusegun G. Ademowo; Tiwalade Adewale Olugbade; Thomas J. Schmidt; Eugene Joseph Verspohl
Methanolic extract and chromatographic fractions of Gongronema latifolium were tested against clinical isolates of Plasmodium falciparum-, P. yoelii nigeriensis-infected mice, chloroquine-sensitive (D6) and chloroquine-resistant (W2) P. falciparum clones. The isolates, characterized as a 1:1 mixture of α-amyrin and β-amyrin cinnamates (1a/1b), lupenyl cinnamate (2) and lupenyl acetate (3), were assayed using the clones. Extract, most active vacuum liquid and column chromatographic fractions had respective ED50 values of 120.85, 32.03, 25.62 mg.kg-1 and IC50 of 36.27, 9.45, 7.05 μg.mL-1, against W2 clones. Lupenyl acetate had 18.96 μg.mL-1, indicating synergistic action of the constituents. Results justified its ethnomedical use for treating malaria.
Journal of Diabetes | 2013
Adeleke Clement Adebajo; Marcus Durojaye Ayoola; Samuel Akintunde Odediran; Adetunji J. Aladesanmi; Thomas J. Schmidt; Eugene Joseph Verspohl
The insulinotropic activity of the combined root and stem of Gongronema latifolium (Asclepiadaceae) was evaluated to justify its African ethnomedicinal use in the management of diabetes.