Bio

Publications


2020

Langat, MK, Ndunda B, Salter C, Odusina BO, Isyaka SM, Mas-Claret E, Onocha PA, Midiwo JO, Nuzillard J-M, Mulholland DA.  2020.  Diterpenoids from the stem bark of Croton megalocarpoides Friis & M. G. Gilbert. Phytochemistry Letters. 39:1-7.
Langat, MK, Djuidje EFK, Ndunda BM, Isyaka SM, Dolan NS, Ettridge GD, Whitmore H, Lopez I, Alqahtani AM, Atiku I, Lobe JS, Mas-Claret E, Crouch NR, Midiwo JO, Mulholland DA, Kamdem AFW.  2020.  The phytochemical investigation of five African Croton species: Croton oligandrus, Croton megalocarpus, Croton menyharthii, Croton rivularis and Croton megalobotrys. Phytochemistry Letters. 40(2020):148-155.chemistry_of_five_croton_species_phytolletters_2020.pdf

2017

Omosa, LK, RW M, O MJ, EK O, R M, B N, R B, Heydenreich M, H A, E K, EK O, RA O, A Y.  2017.  Antiplasmodial activities of the stem bark extract and compounds of Zanthoxylum gilletii (De wild) P.G. Waterman. Pharmacognosy Communications. 7(1):41-46.
Aldhaher, A, Langat M, Ndunda B, Chirchir D, Midiwo JO, Njue A, Schwikkard S, Carew M, Mulholland D.  2017.  Diterpenoids from the roots of Croton dichogamus Pax. Phytochemistry . 144(2017):1-8.

2016

Ndunda, BE, MBOROKI GUANTAI.  2016.  TCT 332: CHEMISTRY SUBJECT METHODS TEACHING MODULE.
Ndunda, B, Langat MK, Mulholland DA, Eastman H, Jacob MR, Khan SI, A.Walker L, Muhammad I, Kerubo LO, Midiwo JO.  2016.  New ent-Clerodane and Abietane Diterpenoids from the Roots of Kenyan Croton megalocarpoides Friis & M.G. Gilbert. Planta Med. 82(2016):1079-1086.
Omosa, LK, Akala H, Kenanda EO, Ndunda B.  2016.  Variability of Surface Exudates of Dodonaea angustifolia L.f, Antioxidant and Antiplasmodial activities of the compounds. Journal of Natural Sciences Research. 6(10):2224-3186.

2015

Wanjohi, JM, Ndunda B.  2015.  SCH 404: NATURAL PRODUCTS CHEMISTRY Teaching Module.
Ndunda, BE, Langat MK, Midiwo JO, Omosa LK.  2015.  Diterpenoid Derivatives of Kenyan Croton sylvaticus. NPC. 10(4):557-558.

2014

Ndunda, BE, Midiwo JO, Omosa LK, LANG’AT MK.  2014.  PHYTOCHEMISTRY AND BIOACTIVITY INVESTIGATIONS OF THREE KENYAN CROTON SPECIES. , Nairobi-Kenya: University of Nairobi
Omosa, LK, Amugune B, Ndunda B, Milugo TK, Heydenreich M, Yenesew A, Midiwo JO.  2014.  Antimicrobial flavonoids and diterpenoids from Dodonaea angustifolia. South African Journal of Botany. Abstract

The surface exudates of the leaves of Dodonaea angustifolia from Ngong forest population (6 km from Nairobi city center, Kenya) demonstrated antimicrobial activity against Gram-negative (Escherichia coli), Gram-positive (Staphylococcus aureus and Bacillus pumilus) bacteria and the fungus Sacchromyces cerevisiae. Chromatographic separation of the exudates yielded eight methylated flavonoids; 5-hydroxy-3, 4′,7-trimethoxyflavone (1), 3,5-dihydroxy-4′,7-dimethoxyflavone (2), santin (3), kumatakenin (4), rhamnocitrin (5), isokaempferide (6), 3,4′,5,7, tetrahydroxy-6-methoxyflavone (7), pinocembrin (8); two clerodanes, dodonic acid (9) and 2β-hydroxyhardwickiic acid (10) and one labdane; (ent-3β,8α)-15,16-epoxy-13(16),14-labdadiene-3,8-diol (11) diterpenoids. The flavonoid aglycones; 6, 7 and the clerodane diterpenoids; 9 and 10 and labdane diterpenoid, 11 were isolated for the first time from this plant species. The structures of the isolated compounds were identified using ultraviolet (UV), mass spectroscopy (MS), one dimension (1D) and two dimension (2D) nuclear magnetic resonance (NMR) spectroscopy and by comparison of the spectral data with literature. The quercetin derivative, 3,4′,5-trihydroxy-3′,7-dimethoxyflavone (12) showed broad spectrum antibacterial activities against E. coli and B. pumilus with minimum inhibition concentration (MIC) values less than 31.25 μg/well and against S. aureus with MIC below 62.5 μg/well. This compound showed poor antifungal activity against S. cerevisiae (MIC < 500 μg/well). Good antifungal activities were observed for 5,4′-dihydroxy-7-methoxyflavanone (13) and hautriwaic acid lactone (14) against S. cerevisiae with MIC values less than 7.8 μg/well. The most active antifungal compound was 5,7-dihydro-3,4′,6-trimethoxyflavone (3, santin) with an MIC value less than 3.9 μg/well against S. cerevisiae. The rest of the compounds exhibited weak to moderate activities. For comprehensive structure activity relationship studies (SAR), hautriwaic acid lactone (14), hautriwaic acid (15), penduletin (16) isolated from the surface exudates of D. angustifolia from Voi (200 km from Mombasa city center, Kenya) and 12 and 13 from Senecio roseiflorus isolated earlier were included in the bioassays.

2013

2007

2005

Ndunda, B, Chabbra S, Langat-Thoruwa C, Akenga T.  2005.  Isolation and Characterization of Compounds from Kenyan Medicinal Plants of the Genus Croton. , JUJA-KENYA: JKUAT

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