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Natural Product Research
Formerly Natural Product Letters
Volume 37, 2023 - Issue 17
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Research Articles

Secondary metabolites of the leaves of Tricalysia atherura N. Hallé (Rubiaceae) and their potential antiplasmodial activity

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Pages 2830-2840 | Received 01 Mar 2022, Accepted 08 Oct 2022, Published online: 25 Oct 2022

References

  • Agata I, Hatano T, Nishibe S, Okuda T. 1988. Rabdosiin: a new rosmarinic acid dimer with a lignin skeleton from Rabosia japonica. Chem Pharm Bull. 36(8):3223–3225.
  • Akbar E, Malik A. 2002. Antimicrobial triterpenes from Debregeasia salicifolia. Nat Prod Lett. 16(5):339–344.
  • Akhtar N, Malik A, Ali SN, Kazmi SU. 1994. Rubrinol, a new antibacterial triterpenoid from Plumeria rubra. Fitoterapia. 65:162–166.
  • Awouafack MD, Tane P, Morita H. 2018. Tricalycoside, a new cerebroside from Tricalysia coriacea (Rubiaceae). Chem Biodiv. 15:1–6.
  • Barreiro EJ. 1990. Produtos naturais bioativos de origem vegetal e o desenvolvimento de fármacos. Quím Nova. 13:29–39.
  • Bartlett MF, Sklar R, Taylor WI, Schlittler E, Amai RLS, Beak P, Bringi NV, Wenkert E. 1962. Rauwolfia alkaloids. XXXVIII.1 Stereospecific degradations leading to the absolute configurations and structures of ajmaline, sarpagine and corynantheidine. J Am Chem Soc. 84(4):622–630.
  • Battersby AR, Yeowell DA. 1964. Alkaloids of calabash-curare and Strychnos species. Part III. Structure and absolute stereochemistry of macusine-A, macusine-B, and macusine-C. J Chem Soc. 0:4419–4427.
  • Bitombo AN, Zintchem AA, Atchadé AT, Ndedi EDFM, Khan A, Bikobo DSN, Pegnyemb DE, Bochet CG. 2022. Antimicrobial and cytotoxic activities of indole alkaloids and other constituents from the stem barks of Rauvolfia caffra Sond (Apocynaceae), Nat Prod Res. 36(6): 1467–1475.
  • Bouquet A. 1972. Plantes médicinales du Congo-Brazzaville. Uvariopsis, Pauridiantha, Diospyros. O.R.S.T.O.M, Paris, p 113. (Travaux et Documents de l'ORSTOM; 13). Th.: Botanique: Paris.
  • Bridson DM, Verdcourt B. 2003. Rubiaceae. Flora Zambesiaca 5(3):379–720. Royal Botanic Gardens, Kew, UK.
  • Brown RT, Charalambides AA. 1974. 5α-Carboxytetrahydroalstonine. Tetrahedron Lett. 17:1649–1652.
  • Bruschi P, Morganti M, Mancini M, Signorini MA. 2011. Traditional healers and laypeople: a qualitative and quantitative approach to local knowledge on medicinal plants in Muda (Mozambique). J Ethnopharmacol. 138(2):543–563.
  • De Silva KTD, King D, Smith GN. 1971. J Chem Soc., Chem Commun. 16:908–909.
  • Elliot S. 1986. Pharmacy needs tropical forests. Manuf Chem. 57:31–34.
  • Evina JN, Bikobo DSN, Zintchem AA, Nyemeck NM, IINdedi EDFM, Diboué PHB, Nyegue MA, Atchadé AT, Pegnyemb DE, Koert U, et al. 2017. In vitro antitubercular activity of extract and constituents from the stem bark of Disthemonanthus benthamianus. Braz J Pharmacol. 27(6):739–743.
  • Farias FM. 2006. [Psychotria myriantha müll arg. (Rubiaceae): Caracterização dos alcalóides e avaliação das atividades antiquimiotáxica e sobre o sistema nervoso central]. [Ph.D. Thesis]. Porto Alegre, RS, Brazil: Universidade Federal do Rio Grande do Sul.
  • Gołembiewska E, Skalicka-Wózniak K, Głowniak K. 2013. Methods for the isolation and identification of triterpenes and sterols in medicinal plants. Curr. Issues Pharm Med Sci. 26:26–32.
  • Greve HL, Kaiser M, Brun R, Schmidt TJ. 2017. Terpenoids from Oleo-Gum-Resin of Boswellia serrata and their antiplasmodial effects in vitro. Planta Med. 83(14-15):1214–1226.
  • He DH, Otsuka H, Hirata E, Shinzato T, Bando M, Takeda Y. 2002. Tricalysiosides A − G: rearranged ent-kauranoid glycosides from the leaves of Tricalysia dubia. J Nat Prod. 65(5):685–688.
  • Ibrahim SRM, Mohamed GA, Shaala LA, Banuls LMY, Van Goietsenoven G, Kiss R, Youssef DTA. 2012. New ursane-type triterpenes from the root bark of Calotropis procera. Phytochem Lett. 5(3):490–495.
  • Irungu BN, Orwa JA, Gruhonjic A, Fitzpatrick PA, Landberg G, Kimani F, Midiwo J, Erdélyi M, Yenesew A. 2014. Constituents of the roots and leaves of Ekebergia capensis and their potential antiplasmodial and cytotoxic activities. Molecules. 19(9):14235–14246.
  • Khedr AIM, Ibrahim SRM, Mohamed GA, Ahmed HEA, Ahmad AS, Ramadan MA, Abd El-Baky AE, Yamada K, Ross SA. 2016. New ursane triterpenoids from Ficus pandurata and their binding affinity for human cannabinoid and opioid receptors. Arch Pharm Res. 39(7):897–911.
  • Kiang AK, Loh SK, Demanczyk M, Gemenden CW, Papariello GJ, Taylor WI. 1966. The structures of peraksine (RP-5) and RP-7 constituents of the leaves and stems of Rauwolfia perakensis. Tetrahedron. 22(10):3293–3300.
  • Kim KH, Choi SU, Lee KR. 2012. Cytotoxic triterpenoids from Berberis koreana. Planta Med. 78(1):86–89.
  • Laurens MB. 2020. RTS,S/AS01 vaccine (MosquirixTM): an overview. Hum Vaccines Immunother. 16(3):480–489.
  • Li LQ, Li J, Huang Y, Wu Q, Deng SP, Su XJ, Yang RY, Huang JG, Chen ZZ, Li S. 2012b. Lignans from the heartwood of Streblus asper and their inhibiting activities to hepatitis B virus. Fitoterapia. 83(2):303–309.
  • Lim QY, Tan SP, Tan HY, Liew WK, Lau YL, Nafiah MA. 2021. Compounds Isolated from Bark of Phyllanthus acidus (L.) Skeels. Malaysian J Chem. 23:165–172.
  • Li J, Tang MJ, Wu Q, Chen H, Niu XT, Guan XL, Li J, Deng SP, Su XJ, Yang RY. 2012a. Water-soluble Constituents of the Heartwood of Streblus asper. Nat Prod Com. 7:497–500.
  • Mabberley DJ. 1990. The plant-book: a portable dictionary of the vascular plants utilizing Kubitzki’s the families and genera of vascular plants.
  • Mahato SB, Kundu AP. 1994. 13C NMR spectra of pentacyclic triterpenoids – acompilation and some salient features. Phytochemistry. 37(6):1517–1575.
  • Mongrand S, Badoc A, Patouille B, Lacomblez C, Chavent M, Bessoule JJ. 2005. Chemotaxonomy of the Rubiaceae family based on leaf fatty acid composition. Phytochemistry. 66(5):549–559.
  • Moshi MJ, Otieno DF, Weisheit A. 2012. Ethnomedicine of the Kagera Region, North Western Tanzania. Part 3: plants used in traditional medicine in Kikuku Village, Muleba District. J Ethnobiol Ethnomed. 8(2012):14.
  • Nishimura K, Hitotsuyanagi Y, Sugeta N, Fukaya H, Aoyagi Y, Hasuda T, Kinoshita T, Takeya K. 2007. Tricalysiamides A − D, Diterpenoid Alkaloids from Tricalysia dubia. J Nat Prod. 70(5):758–762.
  • Nishimura K, Hitotsuyanagi Y, Sugeta N, Sakakura KI, Fujita K, Fukaya H, Aoyagi Y, Hasuda T, Kinoshita T, He DH, et al. 2006. Tricalysiolides A-F, new rearranged ent-kaurane diterpenes from Tricalysia dubia. Tetrahedron. 62(7):1512–1519.
  • Nogueira PCN, Araújo RM, Viana GSB, de Araújo DP, Braz Filho R, Silveira ER. 2014. Plumeran Alkaloids and Glycosides from the Seeds of Aspidosperma pyrifolium Mart. J Braz Chem Soc. 25:2108–2120.
  • Parmar VS, Jain SC, Gupta S, Talwar S, Rajwanshi VK, Kumar R, Azim A, Malhotra S, Kumar N, Jain R, et al. 1998. Polyphenols and alkaloids from Piper species. Phytochemistry. 49(4):1069–1078.
  • Pereira CG, Meireles MAA. 2010. Supercritical fluid extraction of bioactive compounds: fundamentals, applications and economic perspectives. Food Bioprocess Technol. 3(3):340–372.
  • Puteri A, Nugroho AE, Hirasawa Y, Kaneda T, Tougan T, Horii T, Morita H. 2019. Two new sarpagine‑type indole alkaloids and antimalarial activity of 16‑demethoxycarbonyl voacamine from Tabernaemontana macrocarpa Jack. J Nat Med. 73(4):820–825.
  • Rasoanaivo A, Ravi P, Petitjean S, Ratsimamanga-Urverg A, Rakoto R. 1992. Medicinal plants used to treat malaria in Madagascar. J Ethnopharmacol. 37(2):117–127.
  • Robbrecht E. 1987. The African genus Tricalysia A. Rich. (Rubiaceae): 4. A revision of the species of sectio Tricalysia. Bull Nat Plantentuin Belg. 57(1/2):39–208.
  • Silva BP, Parente JP. 2004. New Steroidal Saponins from Rhizomes of Costus spiralis. Z Naturforsch C J Biosci. 59(1-2):81–85.
  • Sonké B, CHeek M, Nambou DM, Robbrecht E. 2002. A new species of Tricalysia A. Rich. (Rubiaceae) from western Cameroon. Kew Bull. 57(3):681–686.
  • Staerk D, Lemmich E, Christensen J, Kharazmi A, Olsen CE, Jaroszewski JW. 2000. Leishmanicidal, antiplasmodial and cytotoxic activity of indole alkaloids from Corynanthe pachyceras. Planta Med. 66(6):531–536.
  • World Health Organization 2004. World health report 2003. Available at http://www.who.int/whr/2003/en.
  • World Health Organization 2020. World Malaria Report. The “World malaria report 2020” at a glance. WHO: Geneva, Switzerland. Available from http://www.who.int/teams/global-malaria-programme/report/world-malaria-report-2020. Accessed on 3rd March, 2021.
  • World Health Organization 2021. WHO recommends groundbreaking malaria vaccine for children at risk. Available from https://who.int/news/item/06-10-2021-who-recommends-groundbreaking-malaria-vaccine-for-children-at-risk. Accessed on 31st October, 2021.
  • Xu WH, Jacob MR, Agarwal AK, Clark AM, Liang ZS, Li XC. 2010. Ent-Kaurane Glycosides from Tricalysia okelensis. Chem Pharm Bull (Tokyo). 58(2):261–264.

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