8
M. ELSBAEY ET AL.
Ali M, Kim D, Seong S, Kim H-R, Jung H, Choi J. 2017. a-Glucosidase and protein tyrosine phos-
phatase 1B inhibitory activity of plastoquinones from marine brown alga Sargassum serratifo-
lium. Mar Drugs. 15(12):368–387.
Chen J, Wang X, Cai Y, Tang M, Dai Q, Hu X, Huang M, Sun F, Liu Y, Xia P. 2013. Bioactivity-
guided fractionation of physical fatigue-attenuating components from Rubus parvifolius
L. Molecules. 18:11624–11638.
Cheng D-L, Cao X-P. 1992. Pomolic acid derivatives from the root of Sanguisorba officinalis.
Phytochem. 31(4):1317–1320.
Cheng S-Y, Wang C-M, Cheng H-L, Chen H-J, Hsu Y-M, Lin Y-C, Chou C-H. 2013. Biological activ-
ity of oleanane triterpene derivatives obtained by chemical derivatization. Molecules. 18(10):
13003–13019.
Ding H, Hu X, Xu X, Zhang G, Gong D. 2018. Inhibitory mechanism of two allosteric inhibitors,
oleanolic acid and ursolic acid on a-glucosidase. Inter J Biol Macromol. 107:1844–1855.
El-Garf I, Grayer RJ, Kite GC, Veitch NC. 1999. Hypolaetin 8-O-glucuronide and related flavonoids
from Lavandula coronopifolia and L. pubescens. Biochem Syst Ecol. 27(8):843–846.
Farshori NN, Al-Sheddi ES, Al-Oqail MM, Hassan WH, Al-Khedhairy AA, Musarrat J, Siddiqui MA.
2015. Hepatoprotective potential of Lavandula coronopifolia extracts against ethanol induced
oxidative stress-mediated cytotoxicity in HepG2 cells. Toxicol Ind Health. 31(8):727–737.
Fatmawati S, Kondo R, Shimizu K. 2013. Structure–activity relationships of lanostane-type triter-
penoids from Ganoderma lingzhi as a-glucosidase inhibitors. Bioorg Med Chem Lett. 23(21):
5900–5903.
Ha C, Bhagavan N-V. 2011. Essentials of Medical Biochemistry: With Clinical Cases. London:
Academic Press.
Lis-Balchin M. 2003. Lavender: the genus Lavandula. London. CRC press.
Lontsi D, Sondengam B, Martin M, Bodo B. 1998. Cecropioic acid, a pentacyclic triterpene from
Musanga cecropioides. Phytochem. 48(1):171–174.
Meresa A, Gemechu W, Basha H, Fekadu N, Teka F, Ashebir R, Tadele A. 2017. Herbal medicines
for the management of diabetic mellitus in Ethiopia and Eretria including their phytochemical
constituents. AJADD. 5:040–058.
ꢁ
ꢁ
Morocho V, Valle A, Garcıa J, Gilardoni G, Cartuche L, Suarez AI. 2018. a-Glucosidase Inhibition
and Antibacterial Activity of Secondary Metabolites from the Ecuadorian Species Clinopodium
taxifolium (Kunth) Govaerts. Molecules. 23(1):146.
Neto CC, Vaisberg AJ, Zhou B-N, Kingston DG, Hammond GB. 2000. Cytotoxic triterpene acids
from the Peruvian medicinal plant Polylepis racemosa. Planta Med. 66(5):483–484.
Ojinnaka CM, Okogun JI, Okorie DA. 1984. Myrianthic acid: a triterpene acid from the rootwood
of Myrianthus arboreus. Phytochem. 23(5):1125–1127.
Rao KR, Rao L, Rao NP. 1990. An A-ring contracted triterpenoid from Hyptis suaveolens.
Phytochem. 29:1326–1329.
Sandjo LP, Rincheval V, Ngadjui BT, Kirsch G. 2011. Cytotoxic effect of some pentacyclic triter-
penes and hemisynthetic derivatives of stigmasterol. Chem Nat Compd. 47(5):731–734.
Seo S, Tomita Y, Tori K. 1975. Carbon-13 NMR spectra of urs-12-enes and application to struc-
tural assignments of components of Isodon japonicus Hara tissue cultures. Tetrahedron Lett.
16(1):7–10.
ꢁ
Sidjui LS, Zeuko’o EM, Toghueo RMK, Note OP, Mahiou-Leddet V, Herbette G, Fekam FB, Ollivier
E, Folefoc GN. 2014. Secondary metabolites from Jacaranda mimosifolia and Kigelia africana
(Bignoniaceae) and their anticandidal activity. Rec Nat Prod. 8:307–311.
Singab AB, El-Gendi OD, Kusano A, Kusano G. 2000. Two New Triterpenic Glucosidates from
Lavandula coronipifolia in Egypt. Nat Med. 54:38–41.
€
ꢀ
ꢀ
Tag O, C¸agır A, Khan IA, Bedir E. 2012. Cleavage of ring A and formation of an unusual nor-tri-
terpene skeleton via the Baeyer–Villiger reaction. Tetrahedron Lett. 53(44):5864–5867.
Thao NP, Luyen BTT, Tai BH, Yang SY, Jo SH, Cuong NX, Nam NH, Kwon YI, Van Minh C, Kim YH.
2014. Rat intestinal sucrase inhibition of constituents from the roots of Rosa rugosa Thunb.
Bioorg Med Chem Lett. 24(4):1192–1196.