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Review Article

Genus Monanthotaxis: a review on distribution, ethnomedicinal uses and phytochemistry

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Received 20 Mar 2023, Accepted 30 Dec 2023, Published online: 23 Jan 2024

References

  • Achenbach H, Hemrich H. 1991. Alkaloids, flavonoids and phenylpropanoids of the West African plant Oxymitra velutina. Phytochem. 30(4):1265–1267. doi:10.1016/S0031-9422(00)95214-2.
  • Arnaud JND, Steve EE, Tamokou J-d-D, Cyrille NT, Harakat D, Laurence V-N, David N. 2020. A new stilbene dimer and other chemical constituents from Monanthotaxis littoralis with their antimicrobial activities. NPS. 26(4):317–325. doi:10.20307/nps.2020.26.4.317.
  • Aye MM, Aung HT, Sein MM, Armijos C. 2019. A review on the phytochemistry, medicinal properties and pharmacological activities of 15 selected Myanmar medicinal plants. Molecules. 24(2):293. doi:10.3390/molecules24020293.
  • Bachewar NP, Thawani VR, Mali SN, Gharpure KJ, Shingade VP, Dakhale GN. 2009. Comparison of safety, efficacy, and cost effectiveness of benzyl benzoate, permethrin, and ivermectin in patients of scabies. Indian J Pharmacol. 41(1):9–14. doi:10.4103/0253-7613.48882.
  • Bernatova I. 2018. Biological activities of (−)-epicatechin and (−)-epicatechin-containing foods: focus on cardiovascular and neuropsychological health. Biotechnol Adv. 36(3):666–681. doi:10.1016/j.biotechadv.2018.01.009.
  • Boustie J, Stigliani J-L, Montanha J, Amoros M, Payard M, Girre L. 1998. Antipoliovirus structure − activity relationships of some aporphine alkaloids. J Nat Prod. 61(4):480–484. doi:10.1021/np970382v.
  • Chang H-S, Chen I-S. 2016. Chemical constituents and bioactivity of Formosan lauraceous plants. J Food Drug Anal. 24(2):247–263. doi:10.1016/j.jfda.2015.10.008.
  • Chepkirui C, Matasyoh JC, Wagara IN, Nakavuma J. 2014. Antifungal activity of flavonoids isolated from Monanthotaxis littoralis against mycotoxigenic fungi from maize. Am J Chem Appl. 1(4):54–60.
  • Chhabra S, Mahunnah B, Mshiu E. 1987. Plants used in traditional medicine in Eastern Tanzania. I. Pteridophytes and angiosperms (Acanthaceae to Canellaceae). J Ethnopharmacol. 21(3):253–277. doi:10.1016/0378-8741(87)90103-6.
  • Choi CW, Song SB, Oh JS, Kim YH. 2015. Antiproliferation effects of selected Tanzania plants. Afr J Tradit Complement Altern Med. 12(2):96–102. doi:10.4314/ajtcam.v12i2.15.
  • Costa EV, Pinheiro MLB, Barison A, Campos FR, Salvador MJ, Maia BHL, Cabral EC, Eberlin MN. 2010. Alkaloids from the bark of Guatteria hispida and their evaluation as antioxidant and antimicrobial agents. J Nat Prod. 73(6):1180–1183. doi:10.1021/np100013r.
  • Dagli S. 2002. Studies in natural products [PhD Thesis]. United Kingdom: University of Glasgow.
  • De la Cruz-Chacón I, González-Esquinca AR, Fefer PG, Garcia LFJ. 2011. Liriodenine, early antimicrobial defence in Annona diversifolia. Z Naturforsch C J Biosci. 66(7-8):377–384. doi:10.1515/znc-2011-7-809.
  • Dinica RM, Sandu C, Dediu Botezatu AV, Cazanevscaia Busuioc A, Balanescu F, Ionica Mihaila MD, Dumitru CN, Furdui B, Iancu AV. 2021. Allantoin from valuable Romanian animal and plant sources with promising anti-inflammatory activity as a nutricosmetic ingredient. Sustainability. 13(18):10170. doi:10.3390/su131810170.
  • Farhadi F, Khameneh B, Iranshahi M, Iranshahy M. 2019. Antibacterial activity of flavonoids and their structure–activity relationship: an update review. Phytother Res. 33(1):13–40. doi:10.1002/ptr.6208.
  • Fleischer TC, Waigh RD, Waterman PG. 1997. Bisabolene sesquiterpenes and flavonoids from Friesodielsia enghiana. Phytochem. 44(2):315–318. doi:10.1016/S0031-9422(96)00527-4.
  • Frausin G, Lima RBS, Hidalgo A, Maas P, Pohlit AM. 2014. Plantas da familia Annonaceae tradicionalmente usadas como antimaláricos: uma revisão. Rev Bras Frutic. 36(spe1):315–337. doi:10.1590/S0100-29452014000500038.
  • Guo X, Hoekstra PH, Tang CC, Thomas DC, Wieringa JJ, Chatrou LW, Saunders RM. 2017. Cutting up the climbers: evidence for extensive polyphyly in Friesodielsia (Annonaceae) necessitates generic realignment across the tribe Uvarieae. Taxon. 66(1):3–19. doi:10.12705/661.1.
  • Hoekstra PH, Chatrou LW, Wieringa JJ. 2014. A new species of Monanthotaxis from Gabon with a unique inflorescence type for Annonaceae. Phytotaxa. 186(2):106–112. doi:10.11646/phytotaxa.186.2.5.
  • Hoekstra PH, Wieringa JJ, Chatrou LW. 2016. A nonet of novel species of Monanthotaxis (Annonaceae) from around Africa. PhytoKeys. 69(69):71–103. doi:10.3897/phytokeys.69.9292.
  • Hoekstra P, Wieringa J, Maas P, Chatrou L. 2021. Revision of the African species of Monanthotaxis (Annonaceae). Blum - j Plant Tax and Plant Geog. 66(2):107–221. doi:10.3767/blumea.2021.66.02.01.
  • Hongthong S, Kuhakarn C, Jaipetch T, Prabpai S, Kongsaeree P, Piyachaturawat P, Jariyawat S, Suksen K, Limthongkul J, Panthong A, et al. 2015. Polyoxygenated cyclohexene derivatives isolated from Dasymaschalon sootepense and their biological activities. Fitoterapia. 106:158–166. doi:10.1016/j.fitote.2015.09.001.
  • Houghton PJ. 1995. The role of plants in traditional medicine and current therapy. J Altern Complement Med. 1(2):131–143. doi:10.1089/acm.1995.1.131.
  • Ibrahim M, Rasoanaivo LH, Paltinean R, Vlase L, Raharisololalao A, Crisan G. 2016. Phenolic compounds and triterpene identified from Monanthotaxis pilosa Baillon. Int J Chem Stud. 4:22–27.
  • Jolad SD, Hoffmann JJ, Schram KH, Cole JR, Tempesta MS, Bates RB. 1981. Structures of zeylenol and zeylena, constituents of Uvaria zeylanica (Annonaceae). J Org Chem. 46(21):4267–4272. doi:10.1021/jo00334a033.
  • Joseph CC, Magadula JJ, Nkunya MH. 2007. A novel antiplasmodial 3′, 5′-diformylchalcone and other constituents of Friesodielsia obovata. Nat Prod Res. 21(11):1009–1015. doi:10.1080/14786410701194310.
  • Joshi B, Gawad D, Fuhrer H. 1979. Revised structures of pipoxide and pipoxide chlorohydrin. Tetrahedron Lett. 20(26):2427–2430. doi:10.1016/S0040-4039(01)86310-3.
  • Laryea MK, Borquaye LS. 2019. Antimalarial efficacy and toxicological assessment of extracts of some Ghanaian medicinal plants. J Parasit Res. 2019:1–9. doi:10.1155/2019/1630405.
  • Liang G-Y, Gray AI, Thomas DW, Waterman PG. 1988. Polyoxygenated cyclohexane epoxide derivatives from the stem bark of Monanthotaxis buchananii. Phytochem. 27(12):3857–3860. doi:10.1016/0031-9422(88)83032-2.
  • Maeda G, van der Wal J, Gupta AK, Munissi JJE, Orthaber A, Sunnerhagen P, Nyandoro SS, Erdélyi M. 2020. Oxygenated cyclohexene derivatives and other constituents from the roots of Monanthotaxis trichocarpa. J Nat Prod. 83(2):210–215. doi:10.1021/acs.jnatprod.9b00363.
  • Makhuvele R, Foubert K, Apers S, Pieters L, Verschaeve L, Elgorashi E. 2018. Antimutagenic constituents from Monanthotaxis caffra (Sond.) Verdc. J Pharm Pharmacol. 70(7):976–984. doi:10.1111/jphp.12918.
  • Mevy J, Bessiere J, Pelissier Y, Masotti V, Ruzzier M, Rabier J, Viano J. 2004. Composition of the volatile constituents of the aerial parts of an endemic plant of Ivory Coast, Monanthotaxis capea (EG & A. Camus) Verdc. Flavour & Fragrance J. 19(6):526–528. doi:10.1002/ffj.1329.
  • Mligo C. 2015. Conservation of plant biodiversity of Namatimbili forest in the southern coastal forests of Tanzania. Int J Biodivers Conserv. 7(3):148–172. doi:10.5897/IJBC2014.0771.
  • Mohammadhosseini M, Frezza C, Venditti A, Akbarzadeh A. 2019. Ethnobotany and phytochemistry of the genus Eremostachys Bunge. COC. 23(17):1828–1842. doi:10.2174/1385272823666191007161550.
  • Mohammadhosseini M, Venditti A, Akbarzadeh A. 2021. The genus Perovskia Kar.: ethnobotany, chemotaxonomy and phytochemistry: a review. Toxin Rev. 40(4):484–505. doi:10.1080/15569543.2019.1691013.
  • Mouthe KGP, Fotsing KS, Dzouemo LCM, Happi G, Fogue Kouam S, Tchouankeu JC. 2021. Phytochemistry, traditional uses, and pharmacology of the genus Ekebergia (Meliaceae): a review. Trends Phytochem Res. 5:110–125.
  • Mulholland D, Naidoo N, Hutchings A, Lavaud C, Massiot G. 2000. Crotepoxide, a cyclohexane diepoxide from Monanthotaxis caffra. Biochem Syst Ecol. 28(6):595–597. doi:10.1016/s0305-1978(99)00099-x.
  • Mungai NN. 2015. Antiplasmodial and phytochemical investigation of Monanthotaxis parvifolia (oliv.) verdc ssp. Kenyensis verdc (annonaceae) [PhD Thesis]. Kenya: University of Nairobi.
  • Nguetse JAD, Wonkam AKN, Ekom SE, Harakat D, Voutquenne-Nazabadioko L, Ngnokam D. 2020. Monanthosin, a new monoterpene from the leaves of Monanthotaxis littoralis (Annonaceae) with the antimicrobial and antioxidant activities of chemical constituents. J Appl Chem. 13:1–9.
  • Nishiyama Y, Ishida Y, Yoshino T, Moriyasu M, Kato A, Juma F, Mathenge S, Mutiso P. 2014. Isoquinoline alkaloids from Monanthotaxis trichocarpa. Jpn J Pharmacog. 68(1):20–22.
  • Nkunya MH, Weenen H, Bray DH, Mgani QA, Mwasumbi L. 1991. Antimalarial activity of Tanzanian plants and their active constituents: the genus Uvaria1. Planta Med. 57(4):341–343. doi:10.1055/s-2006-960113.
  • Nkunya MH, Weenen H, Koyi NJ, Thijs L, Zwanenburg B. 1987. Cyclohexene epoxides,(+)-pandoxide,(+) β-senepoxide and (−)-pipoxide, from Uvaria pandensis. Phytochem. 26(9):2563–2565. doi:10.1016/S0031-9422(00)83878-9.
  • Nordin N, Majid NA, Hashim NM, Rahman MA, Hassan Z, Ali HM. 2015. Liriodenine, an aporphine alkaloid from Enicosanthellum pulchrum, inhibits proliferation of human ovarian cancer cells through induction of apoptosis via the mitochondrial signaling pathway and blocking cell cycle progression. Drug Des Devel Ther. 9:1437–1448. doi:10.2147/DDDT.S77727.
  • Nyandoro SS, Maeda G, Munissi JJE, Gruhonjic A, Fitzpatrick PA, Lindblad S, Duffy S, Pelletier J, Pan F, Puttreddy R, et al. 2019. A new benzopyranyl cadenane sesquiterpene and other antiplasmodial and cytotoxic metabolites from Cleistochlamys kirkii. Molecules. 24(15):2746. doi:10.3390/molecules24152746.
  • Olaoluwa O, Taiwo O, Nahar L, Sarker SD. 2022. Ethnopharmacology, phytochemistry and biological activities of selected African species of the genus Ficus. Trends Phytochem Res. 6:46–69.
  • Pakia M, Cooke J, Van Staden J. 2003. The ethnobotany of the Midzichenda tribes of the coastal forest areas in Kenya: 2. Medicinal plant uses. S Afr J Bot. 69(3):382–395. doi:10.1016/S0254-6299(15)30321-5.
  • Parmena D, Mgina C, Joseph C. 2012. Composition of non volatile oils and antimicrobial activities of extracts from Monanthotaxis discolor, and an undescribed Uvariondedron species. Tanzan J Sci. 38:221–231.
  • Rakotonandrasana S, Rakotondrafara A, Rakotondrajaona R, Rasamison V, Ratsimbason M. 2017. Plantes médicinales des formations végétales de la baie de Rigny-Antsiranana à Madagascar. Bois Trop. 331:55–65. doi:10.19182/bft2017.331.a31326.
  • Sobiecki J-F. 2002. A preliminary inventory of plants used for psychoactive purposes in southern African healing traditions. Trans R Soc South Africa. 57(1-2):1–24. doi:10.1080/00359190209520523.
  • Starks CM, Williams RB, Rice SM, Norman VL, Lawrence JA, Goering MG, O’Neil-Johnson M, Hu J-F, Eldridge GR. 2012. Polyoxygenated cyclohexene derivatives from Monanthotaxis congoensis. Phytochem. 74:185–189. doi:10.1016/j.phytochem.2011.10.014.
  • Sumary DP, Mgina CA, Joseph CC. 2020. Isolation and antimicrobial activities of a novel discolornolide and other compounds from Monanthotaxis discolor. Nat Prod Res. 34(22):3163–3168. doi:10.1080/14786419.2018.1553168.
  • Takeuchi Y, Shi Q-W, Sugiyama T, Oritani T. 2002. Polyoxygenated cyclohexenes from the Chinese tree, Uvaria purpurea. Biosci Biotechnol Biochem. 66(3):537–542. doi:10.1271/bbb.66.537.
  • Verdcourt B. 1962. Two interesting plant records from East Africa. Journal of East African Natural History. 105(1):37–40. https://hdl.handle.net/10520/AJA00128317_571.
  • Verdcourt B. 1971. Notes on East African Annonaceae. Kew Bull. 25(1):1. doi:10.2307/4103132.
  • Waterman PG, Pootakahm K. 1979. Chemical Studies on the Annonaceae–VI. The Alkaloids of the Stem and Fruit of Monanthotaxis cauliflora1. Planta Med. 37(11):247–252. doi:10.1055/s-0028-1097335.
  • Weenen H, Nkunya MH, Mgani QA, Posthumus MA, Waibel R, Achenbach H. 1991. Tanzanene, a spiro benzopyranyl sesquiterpene from Uvaria tanzaniae Verdc. J Org Chem. 56(20):5865–5867. doi:10.1021/jo00020a030.
  • Wollenweber E, Kohorst G, Mann K, Bell JM. 1985. Leaf gland flavonoids in Comptonia peregrina and Myrica pensylvanica (Myricaceae). J Plant Physiol. 117(5):423–430. doi:10.1016/S0176-1617(85)80049-3.
  • Yang K, Jin G, Wu J. 2007. The neuropharmacology of (-)-stepholidine and its potential applications. Curr Neuropharmacol. 5(4):289–294. doi:10.2174/157015907782793649.
  • Yong-Hong L, Li-Zhen X, Shi-Lin Y, Jie D, Yong-Su Z, Min Z, Nan-Jun S. 1997. Three cyclohexene oxides from Uvaria grandiflora. Phytochem. 45(4):729–732. doi:10.1016/S0031-9422(97)00026-5.
  • Zahari A, Ablat A, Sivasothy Y, Mohamad J, Choudhary MI, Awang K. 2016. In vitro antiplasmodial and antioxidant activities of bisbenzylisoquinoline alkaloids from Alseodaphne corneri Kosterm. Asian Pac J Trop Med. 9(4):328–332. doi:10.1016/j.apjtm.2016.03.008.
  • Zheng Z, Qiao Z, Gong R, Wang Y, Zhang Y, Ma Y, Zhang L, Lu Y, Jiang B, Li G, et al. 2016. Uvangoletin induces mitochondria-mediated apoptosis in HL-60 cells in vitro and in vivo without adverse reactions of myelosuppression, leucopenia and gastrointestinal tract disturbances. Oncol Rep. 35(2):1213–1221. doi:10.3892/or.2015.4443.

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