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Natural Product Research
Formerly Natural Product Letters
Volume 36, 2022 - Issue 17
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Research Articles

Antibacterial and cytotoxic activities of undescribed cassiaric acid and other constituents from Cassia arereh stem barks

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Pages 4324-4333 | Received 11 Feb 2021, Accepted 11 Sep 2021, Published online: 27 Sep 2021

References

  • Ado KGS, Salihu L. 2014. Fundulopanchax gardneri Test: A Convenient Method of Bioassay for Active Constituents of Natural Products. Nat Prod Chem Res. 2:4. DOI: 10.4172/2329-6836.1000133
  • Akanbi BO, Nnakaogu CJ. 2012. Phytochemical screening and antimicrobial property of Cassia arereh. Researcher. 4:96–100.
  • Arbonnier M. 2004. Trees, shrubs and lianas of West African Dry Zones, CIRAD Margraf publishers GMBH MNHN, Côte d'ivoire.
  • Bisoli E, Garcez WS, Hamerski L, Tieppo C, Garcez FR. 2008. Bioactive pentacyclic triterpenes from the stems of Combretum laxum. Molecules. 13(11):2717–2728.
  • Cháirez-Ramírez MH, Moreno-Jiménez MR, González-Laredo RF, Gallegos-Infante JA, Rocha-Guzmán NE. 2016. Lupane-type triterpenes and their anti-cancer activities against most common malignant tumors: a review. EXCLI J. 15:758–771.
  • Chaniad P, Sudsai T, Septama AW, Chukaew A, Tewtrakul S. 2019. Evaluation of anti-HIV-1 integrase and anti-inflammatory activities of compounds from Betula alnoides Buch-Ham. Adv Pharmacol Sci. 2019:2573965..
  • Culioli G, Mathe C, Archier P, Vieillescazes C. 2003. A lupane triterpene from frankincense (Boswellia sp., Burseraceae). Phytochemistry. 62(4):537–541.
  • De N, Maori L, Ardo H. 2009. A study on antimicrobial effect of extracts of Cassia arereh (Del.) on some clinical isolates. J Med Plants Res. 3:116–119.
  • dos Santos EO, Meira M, do Vale AE, David JM, de Queiróz LP, David JP. 2012. Isolation and Characterization of New Ceramides from Aerial Parts of Lepidaploa Cotoneaster. Nat Prod Commun. 7(6):781–783.
  • Fauchère J-L. 2002. Bactériologie générale et médicale, Editions Ellipses/Broché : Editions Ellipses: Paris.
  • GLOBOCAN. 2012. International Agency for Research on Cancer. http://globocan.iarc.fr/Default.aspx.
  • Gossan DP, Alabdul Magid A, Yao-Kouassi PA, Josse J, Gangloff SC, Morjani H, Voutquenne-Nazabaioko L. 2016. Antibacterial and cytotoxic triterpenoids from the roots of Combretum racemosum. Fitoterapia. 110:89–95.
  • Gezici S, Şekeroğlu N. 2019. Current perspectives in the application of medicinal plants against cancer: novel therapeutic agents. ACAMC. 19(1):101–111.
  • Hay JD, Morrison WR. 1973. Positional isomers of cis and trans monoenoic acids from ox (steer) perinephric fat. Lipids 8:94–95.
  • Honda M, Ueda Y, Sugiyama S, Komori T. 1991. Synthesis of a new cerebroside from a Chondropsis sp. Sponge. Chem Pharm Bull. 39(6):1385–1391.
  • Imam H, Abd Alla AEWH, Yagi Abd Alla SM. 2013. Evaluation of the larvicidal, antiplasmodial and cytotoxicity properties of Cassia arereh Del. Stem Bark. Europ J Med Plants. 1:78–87.
  • Jacob DL, Odeh SO, Otsapa PBL. 2002. Preliminary in vivo studies of the anti-ulcer effects of the crude seed and leaves extracts of Cassia occidentalis in albino Wistar rats. J Med Trop. 2:15–18.
  • Khedr AIM, Ibrahim SRM, Mohamed GA, Yamada K, Ross SA. 2018. Panduramides A-D, new ceramides from Ficus pandurata fruits. Phytochem Lett. 23:100–105.
  • Kojima H, Sato N, Hatano A, Ogura H. 1990. Sterol glucosides from Prunella vulgaris. Phytochemistry. 29(7):2351–2355.
  • Moradi S, Hasani MT, Darvish L, Roozbeh N. 2017. Evaluating cervico vaginal infections and cervical cancer in women with low socioeconomic levels. Iran J Public Health. 46:867–868.
  • Mosmann T. 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 65(1-2):55–63.
  • Musa SM, Abdelrasool FE, Elsheikh EA, Ahmed LAMN, Mahmoud ALE, Yagi SM. 2011. Ethnobotanical study of medicinal plants in the Blue Nile State, South-eastern Sudan. J Med Plants Res. 17:4287–4297.
  • Nana F, Sandjo LP, Keumedjio F, Ambassa P, Malik R, Kuete V, Rincheval V, Choudhary MI, Ngadjui BT. 2012. Ceramides and cytotoxic constituents from Ficus glumosa Del. (Moraceae). J Braz Chem Soc. 23(3):482–487.
  • Ngono BD, Nkot JL, Mosset P, Atchade AT, Ndongo JT, Pemha R, Pegnyemb DE. 2011. Acylsteryl glycosides and other constituents from Campylospermum densiflorum (Ochnaceae). Rasayan J Chem. 4:753–763.
  • Ngulde SI, Sandabe UK, Hussaini IM. 2015. Ethnobotanical survey of anticancer plants in Askira/Uba local government area of Borno State, Nigeria. Afr J Pharm Pharmacol. 5:123–130.
  • Ngulde SI, Sanni S, Sandabe UK, Sani D. 2010. Phytochemical and antimicrobial screening of the aqueous extract of Cassia arereh Del. stem-bark. Afr J Pharm Pharmacol. 8:530–534.
  • Ngulde SI, Tijjani MB, Ihopo JM, Ya’uba AM. 2013. Antitrypanosomal Potency of Methanol Extract of Cassia arereh Delile Root Bark in Albino Rats. Int J Drug Res Technol. 1:1–7.
  • O’Brien PJ, Siraki AG, Shangari N. 2005. Aldehyde sources, metabolism, molecular toxicity mechanisms, and possible effects on human health. Crit Rev Toxicol. 35(7):609–662.
  • Olusola A, Olutayo O, Afolayan M, Olakunle F, Edah AO. 2011. Elemental analysis and anti-microbial potentials of the leaf extract of Cassia arereh Del. Int. Res. J. Pharm. Pharmacol. 8:188–193.
  • Parkin DM, Bray F, Jemal J, Ferlay A. 2014. Cancer in Africa 2012. Cancer Epidemiol Biomarkers Prev. 23(6):953–966.
  • Peng W, Huo G, Zheng L, Xiong Z, Shi X, Peng D. 2019. Two new oleanane derivatives from the fruits of Leonurus japonicas and their cytotoxic activities. J Nat Med. 73:252–256.
  • Pereira FBM, Domingues FMJ, Silva AMS. 1996. Triterpenes from Acacia dealbata. Nat Prod Lett. 8(2):97–103.
  • Prakash CVS, Prakash I. 2012. Isolation and structural characterization of lupane triterpenes from Polypodium Vulgare. Res J Pharmaceutical Sci. 1:23–27.
  • Rajavel T, Mohankumar R, Archunan G, Ruckmani K, Devi KP. 2017. Beta sitosterol and Daucosterol (phytosterols identified in Grewia tiliaefolia) perturbs cell cycle and induces apoptotic cell death in A549 cells. Sci Rep. 7(1):3418.
  • Rambabu P, Ganapaty S, Ramana VS. 2011. Isolation and characterization of triterpènes from zizyphus glabrata. Int J Chem Sci. 9:1014–1024.
  • Rungsimakan S, Rowan MG. 2014. Terpenoids, flavonoids and caffeic acid derivatives from Salvia viridis L. cvar. Blue Jeans. Phytochemistry. 108:177–188.
  • Schmidt J, Himmelreich U, Adam G. 1995. Brassinosteroids, sterols and lup-20(29)-en-2α,3β,28-triol from Rheum rhabarbarum. Phytochemistry. 40(2):527–531.
  • Svatos A, Attygalle AB. 1997. Characterization of vinyl-substituted, carbon-carbon double bonds by GC/FT-IR analysis. Anal Chem. 69(10):1827–1836.
  • Selm YA, Litinas KE. 2015. Cytototxic and antimicrobial activities of two new triterpenoids from the peels of local Egyptian Malus domestica L. J Chil Chem Soc. 60(2):2896–2899.
  • Shahat AA, Hidayathulla S, Khan AA, Alanazi AM, Al Meanazel OT, Alqahtani AS, Alsaid MS, Hussein AA. 2019. Phytochemical profiling, antioxidant and anticancer activities of Gastrocotyle hispida growing in Saudi Arabia. Act Tropic. 191:243–247.
  • Sharma S, Chattopadhyay SK, Singh M, Bawankule DU, Kumar S. 2014. Novel chemical constituents with anti-inflammatory activity from the leaves of Sesbania aculeate. Phytochemistry. 100:132–140.
  • Spek AL, Kojić-Prodić B, Labadie RP. 1984. Structure of (−)-epicatechin: (2R,3R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol, C15H14O6. Acta Crystallogr C Cryst Struct Commun. 40(12):2068–2071.
  • Tacconelli E, Carrara E, Savoldi A, Harbarth S, Mendelson M, Monnet DL, Pulcini C, Kahlmeter G, Kluytmans J, Carmeli Y, et al. 2018. Discovery, research, and development of new antibiotics: the WHO priority list of antibiotic-resistant bacteria and tuberculosis. Lancet Infect Dis. 18(3):318–327.
  • Tian XR, Tang HF, Feng JT, Li YS, Lin HW, Fan XP, Zing X. 2014. Neritinaceramides A–E, New ceramides from the marine bryozoan Bugula neritina inhabiting South China sea and their cytotoxicity. Mar Drugs. 72:1987–2003.
  • Vàzquez LH, Palazon J, Navarro-Ocana A. 2012. The pentacyclic triterpenes α, β amyrins: a review of sources and biological activities. In: Rao W, editor. Phytochemicals – a global perspective of their role in nutrition and health. edited by Venketeshwer Rao published by InTech Janeza Trdine 9, 51000 Rijeka, Croatia. pp. 487–502.
  • World Health Organization, WHO. 2020., Report on cancer: setting priorities, investing wisely and providing care for all. World Health Organization.
  • Zhong SM, Waterman PG, Jeffreys JAD. 1984. Naphthoquinones and triterpenes from african Diospyros species. Phytochemistry. 23(5):1067–1072.

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