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Natural Product Research
Formerly Natural Product Letters
Volume 35, 2021 - Issue 9
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Research Articles

Pentacylic triterpenes from Lavandula coronopifolia: structure related inhibitory activity on α-glucosidase

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Pages 1436-1444 | Received 22 Feb 2019, Accepted 31 Jul 2019, Published online: 21 Aug 2019

References

  • Ait Said L, Zahlane K, Ghalbane I, El Messoussi S, Romane A, Cavaleiro C, Salgueiro L. 2015. Chemical composition and antibacterial activity of Lavandula coronopifolia essential oil against antibiotic-resistant bacteria. Nat Prod Res. 29(6):582–585.
  • Ali M, Kim D, Seong S, Kim H-R, Jung H, Choi J. 2017. α-Glucosidase and protein tyrosine phosphatase 1B inhibitory activity of plastoquinones from marine brown alga Sargassum serratifolium. 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 activity 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 α-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 triterpenoids 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, García J, Gilardoni G, Cartuche L, Suárez AI. 2018. α-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 triterpenes 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 structural assignments of components of Isodon japonicus Hara tissue cultures. Tetrahedron Lett. 16(1):7–10.
  • Sidjui LS, Zeuko'o EM, Toghueo RMK, Noté 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.
  • Tağ Ö, Çağır A, Khan IA, Bedir E. 2012. Cleavage of ring A and formation of an unusual nor-triterpene 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.
  • Urosa A, Marcos IS, Díez D, Lithgow A, Plata GB, Padrón JM, Basabe P. 2015. Synthesis and bioactivity of Luffarin I. Mar Drugs. 13(4):2407–2423.
  • Van De Laar FA, Lucassen PL, Akkermans RP, Van De Lisdonk EH, Rutten GE, Van Weel C. 2005. Alpha-glucosidase inhibitors for patients with type 2 diabetes: results from a Cochrane systematic review and meta-analysis. Diabetes Care. 28(1):154–163.
  • Wang F, Li X-M, Liu J-K. 2009. New terpenoids from Isodon sculponeata. Chem Pharm Bull. 57(5):525–527.
  • Whiteley CG. 1999. Enzyme kinetics: Partial and complete non‐competitive inhibition. Biochem Edu. 27(1):15–18.
  • Woo KW, Han JY, Choi SU, Kim KH, Lee KR. 2014. Triterpenes from Perilla frutescens var. acuta and their cytotoxic activity. Nat Prod Sci. 20:71–75.
  • Wu P, Zheng J, Huang T, Li D, Hu Q, Cheng A, Jiang Z, Jiao L, Zhao S, Zhang K. 2015. Synthesis and evaluation of novel triterpene analogues of ursolic acid as potential antidiabetic agent. PloS One. 10(9):e0138767
  • Zhang B-W, Xing Y, Wen C, Yu X-X, Sun W-L, Xiu Z-L, Dong Y-S. 2017. Pentacyclic triterpenes as α-glucosidase and α-amylase inhibitors: Structure-activity relationships and the synergism with acarbose. Bioorg Med Chem Lett. 27(22):5065–5070.

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