Abiy Yenesew

Abiy Yenesew

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2004 in Phytochemistry
Verified
Journal Article
Closed access
AYAbiy Yenesew
Abiy Yenesew
MIMartha Induli
Martha Induli
SDSolomon Derese
Solomon Derese
JMJacob O. Midiwo
Jacob O. Midiwo
MHMatthias Heydenreich
Matthias Heydenreich
NWNorman C. Waters
Norman C. Waters

1 May 2019 in Phytomedicine
Verified
Journal Article
Closed access
FAFozia A. Adem
Fozia A. Adem
MAMBAVENG T Armelle
MBAVENG T Armelle
KKKuete Kuete
Kuete Kuete
MHMatthias Heydenreich
Matthias Heydenreich
ANAlbert Ndakala
Albert Ndakala
Thomas EfferthThomas Efferth
Thomas Efferth

1 October 2003 in Phytochemistry
Verified
Journal Article
Closed access
AYAbiy Yenesew
Abiy Yenesew
SDSolomon Derese
Solomon Derese
JMJacob O Midiwo
Jacob O Midiwo
HOHellen Oketch-Rabah
Hellen Oketch-Rabah
JLJohn Lisgarten
John Lisgarten
NWNorman C Waters
Norman C Waters

1 July 2003 in Planta Medica
Verified
Journal Article
Closed access
PDF file
AYAbiy Yenesew
Abiy Yenesew
SDSolomon Derese
Solomon Derese
BIBeatrice N. Irungu
Beatrice N. Irungu
JMJacob O. Midiwo
Jacob O. Midiwo
NWNorman C. Waters
Norman C. Waters
MPMartin G. Peter
Martin G. Peter
From the root bark of Erythrina abyssinica a new pterocarpene [3-hydroxy-9-methoxy-10-(3,3-dimethylallyl)pterocarpene] and a new isoflav-3-ene [7,4′-dihydroxy-2′,5′-dimethoxyisoflav-3-ene] were isolated. In addition, the known compounds erycristagallin, licoagrochalcone A, octacosyl ferulate and triacontyl 4-hydroxycinnamate were identified. The structures were determined on the basis of spectroscopic evidence. The crude extract and the flavonoids and isoflavonoids obtained from the roots of this plant showed antiplasmodial activities.

21 July 2020 in Plants
Verified
Journal Article
Open access
PDF file
MKMagrate Kaigongi
Magrate Kaigongi
CLCatherine W. Lukhoba
Catherine W. Lukhoba
YSYaouba Souaibou
Yaouba Souaibou
NMNokwanda Makunga
Nokwanda Makunga
JGJoseph Githiomi
Joseph Githiomi
AYAbiy Yenesew
Abiy Yenesew
Zanthoxylum paracanthum Kokwaro (Rutaceae) is an endemic Kenyan and Tanzanian plant used in folk medicine by local populations. Although other Zanthoxylum species have been studied, only Z. paracantum stem extracts have been profiled, even though the roots are also used as herbal remedies. As root extracts may be another source of pharmaceutical compounds, the CH2Cl2/MeOH (1:1) root bark extract was studied in this report. Eight root bark compounds were isolated and their structural identities were confirmed by mass spectrometry (MS) and nuclear magnetic resonance (NMR) (using COSY, HSQC, NOESY and HMBC) analyses. The structural identities were determined as follows: the fatty acid—myristic acid (1); the sterol—stigmasterol (2); the lignan—sesamin (3); two β-carboline alkaloids—10-methoxycanthin-6-one (6) and canthin-6-one (7); and three phenanthridine alkaloids—8-acetonyldihydrochelerythrine (4), arnottianamide (5) and 8-oxochelerythrine (8). Some of these compounds were identified in the species for the first time. These compounds and the extract were then tested in vitro against methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213) and Candida albicans (ATCC 10231) before tests for antiproliferative activity against the human breast cancer (HCC 1395), human prostate cancer (DU 145) and normal (Vero E6) cell lines were conducted. Minimum inhibition concentration values of 3.91, 1.95, 0.98 and 7.81 µg/mL against MRSA, S. aureus, E. coli and C. albicans, respectively, were recorded. Among the isolates, canthin-6-one was the most active, followed by 10-methoxycanthin-6-one. The root extract and some of the compounds also had antiproliferative activity against the HCC 1395 cell line. Stigmasterol and canthin-6-one had IC50 values of 7.2 and 0.42. The root bark extract also showed activity, at 8.12 µg/mL, against the HCC 1395 cells. Out of the chemical isolates, 10-methoxycanthin-6-one and canthin-6-one showed the strongest inhibition of the DU 145 cells. The root extract had significant antimicrobial and antiproliferative activities, supporting the traditional use of this plant in treating microbial infections and cancer-related ailments.

16 September 2014 in Journal of Natural Products
Verified
Journal Article
Closed access
IGIvan Gumula
Ivan Gumula
JAJohn Patrick Alao
John Patrick Alao
INIsaiah Omolo Ndiege
Isaiah Omolo Ndiege
PSPer Sunnerhagen
Per Sunnerhagen
AYAbiy Yenesew
Abiy Yenesew
MEMate Erdelyi
Mate Erdelyi