Isolation and antibacterial activity of anomanol B and other secondary metabolites from the stem bark of Anonidium mannii (Annonaceae)

References

• Betti JL. 2004. An ethnobotanical study of medicinal plants among the Baka pygmies in the Dja biosphere reserve, Cameroon. Afr Study Monogr. 25(1):1–27.
   Google Scholar
• Bhakuni BS, Kumar A, Balkrishna SJ, Sheikh JA, Konar S, Kumar S. 2012. KOtBu mediated synthesis of phenanthridinones and dibenzoazepinones. Org Lett. 14(11):2838–2841. doi: 10.1021/ol301077y.
   PubMed Web of Science ®Google Scholar
• Demgne OMF, Damen F, Fankam AG, Guefack M-GF, Wamba BEN, Nayim P, Mbaveng AT, Bitchagno GTM, Tapondjou LA, Penlap VB, et al. 2021. Botanicals and phytochemicals from the bark of Hypericum roeperianum (Hypericaceae) had strong antibacterial activity and showed synergistic effects with antibiotics against multidrug-resistant bacteria expressing active efflux pumps. J Ethnopharmacol. 277:114257. doi: 10.1016/j.jep.2021.114257.
   PubMed Web of Science ®Google Scholar
• Dzoyem JP, Hamamoto H, Ngameni B, Ngadjui BT, Sekimizu K. 2013. Antimicrobial action mechanism of flavonoids from Dorstenia species. Drug Discov Ther. 7(2):66–72.
   PubMedGoogle Scholar
• Eloff JN. 1998. A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta Med. 64(8):711–713. doi: 10.1055/s-2006-957563.
   PubMed Web of Science ®Google Scholar
• Fankam AG, Kuiate JR, Kuete V. 2014. Antibacterial activities of Beilschmiedia obscura and six other Cameroonian medicinal plants against multi-drug resistant Gram-negative phenotypes. BMC Complement Altern Med. 14(1):241. doi: 10.1186/1472-6882-14-241.
   PubMedGoogle Scholar
• Hu Q, Gao T, Shi Y, Lei Q, Liu Z, Feng Q, Chen Z, Yu L. 2019. Design, synthesis and biological evaluation of novel 1-phenyl phenanthridin-6 (5H)-one derivatives as anti-tumor agents targeting. Eur J Med Chem. 162:407–422. doi: 10.1016/j.ejmech.2018.11.007.
   PubMed Web of Science ®Google Scholar
• Huang H-C, Liaw C-C, Yang H-L, Hseu Y-C, Kuo H-T, Tsai Y-C, Chien S-C, Amagaya S, Chen Y-C, Kuo Y-H. 2012. Phytochemistry of Lanostane triterpenoids and sterols from Antrodia camphorata. Phytochemistry. 84:177–183. doi: 10.1016/j.phytochem.2012.08.011.
   PubMed Web of Science ®Google Scholar
• Jesus JA, Lago JHG, Laurenti MD, Yamamoto ES, Passero LFD. 2015. Antimicrobial activity of oleanolic nd ursolic acids: an update. Evid Based Complement Alternat Med. 2015:620472. doi: 10.1155/2015/620472.
   PubMed Web of Science ®Google Scholar
• Khatun M, Billah M, Quader MA. 2012. Sterols and sterol glucoside from Phyllanthus species. Dhaka Univ J Sci. 60(1):5–10. doi: 10.3329/dujs.v60i1.10327.
   Google Scholar
• Kuete V. 2010. Potential of Cameroonian plants and derived products against microbial infections: a review. Planta Med. 76(14):1479–1491. doi: 10.1055/s-0030-1250027.
   PubMed Web of Science ®Google Scholar
• Kuete V, Fankam AG, Wiench B, Efferth T. 2013. Cytotoxicity and modes of action of the methanol extracts of six Cameroonian medicinal plants against multidrug-resistant tumor cells. Evid Based Complement Alternat Med. 2013(285903):285903. doi: 10.1155/2013/285903.
   PubMedGoogle Scholar
• Liang D, Hu Z, Peng J, Huang J, Zhu Q. 2013. Synthesis of phenanthridinones via palladium-catalyzed c(sp2)-h aminocarbonylation of unprotected o-arylanilines. Chem Commun (Camb). 49(2):173–175. doi: 10.1039/c2cc36817j.
   PubMed Web of Science ®Google Scholar
• Luo X, Wu S, Ma Y, Wu D. 2000. Tirucallane triterpenoids from Dysoxylum hainanense. Phytochemistry. 54(8):801–805. doi: 10.1016/s0031-9422(00)00172-2.
   PubMed Web of Science ®Google Scholar
• Matchi LJT, Noungoue DT, Kuhn I, Boissier J, Tchouankeu JC, Nothisen M, Garnier D, Ursuegui S, Ngouela SA, Wagner A, et al. 2021. Manniindole, an indole derivative from the roots of Anonidium mannii and combined antischistosomal and enzymatic activities. Nat Prod Res. 35(24):5665–5673. doi: 10.1080/14786419.2020.1824227.
   PubMed Web of Science ®Google Scholar
• Ngaffo CMN, Tankeo SB, Guefack MGF, Wamba BEN, Nayim P, Bonsou IN, Kuete V, Mbaveng AT. 2021. In vitro antibacterial and antibiotic potentiation activities of five edible plant extracts and mode of action against several MDR Gram-negative phenotypes. Invest Med Chem Pharmacol. 4(1):1–14. doi: 10.31183/imcp.2020.00049.
   Google Scholar
• Ngangoue MO, Ngameni B, Ambassa P, Chi GF, Elvis B, Wamba N, Ombito JO, Bojase GM, Fotso GW, Kuete V, et al. 2021. A phenanthridin-6 (5H)-one derivative and a lanostane-type triterpene with antibacterial properties from Anonidium mannii (Oliv). Engl. & Diels (Annonaceae). Nat Prod Res. 35(21):4041–4050. doi: 10.1080/14786419.2020.1758094.
   PubMed Web of Science ®Google Scholar
• Nguemeving JR, Azebaze AGB, Kuete V, Eric CVP, Beng VP, Meyer M, Blond A, Bodo B, Nkengfack AE. 2006. Laurentixanthones A and B, antimicrobial xanthones from Vismia laurentii. Phytochemistry. 67(13):1341–1346. doi: 10.1016/j.phytochem.2006.03.018.
   PubMed Web of Science ®Google Scholar
• Nono EC, Mkounga P, Kuete V, Marat K, Hultin PG, Nkengfack AE. 2010. Pycnanthulignenes A-D, antimicrobial cyclolignene derivatives from the roots of Pycnanthus angolensis. J Nat Prod. 73(2):213–216. doi: 10.1021/np9007393.
   PubMed Web of Science ®Google Scholar
• Silva MADA, Koolen HHF, Barison A, Souza ADLDE, Pinheiro MLB. 2012. Research article steroids and triterpene from the bark of Unonopsis Guatterioides R. E. Fr. (Anonnaceae). Int J Pharm Sci. 4(2):522–523.
   Google Scholar
• Silverstein RM, Webster FX, Kiemle DJ. 2005. Spectrometric identification of organic compounds. New York: john Willy and Sons, Inc; p. 250–255.
   Google Scholar
• Suryawanshi P, Vidyasagar GM. 2016. Phytochemical screening for secondary metabolites of Opuntia dillenii Haw. J Med Plants. 4:39–43.
   Google Scholar
• Tahia F, Sikder AA, Haque MR, Jamil A, Awang K, Al-Mansur A, Rashid MA. 2015. Alkaloids, coumarin and cinnamic acid derivative from Murraya koenigii (Linn.) Spreng. Dhaka Univ J Pharm Sci. 14(1):29–33. doi: 10.3329/dujps.v14i1.23731.
   Google Scholar
• Xia Q, Zhang H, Sun X, Zhao H, Wu L, Zhu D, Yang G, Shao Y, Zhang X, Mao X, et al. 2014. A comprehensive review of the structure elucidation and biological activity of triterpenoids from Ganoderma spp. Molecules. 19(11):17478–17535. doi: 10.3390/molecules191117478.
   PubMed Web of Science ®Google Scholar
• Youmbi LM, Atontsa BCK, Tankeo SB, Nayim P, Wamba ENB, Nganou BK, Bitchagno GTM, Simo IK, Mpetga JDS, Penlap VB, et al. 2020. Antibacterial potential and mechanism of action of botanicals and phytochemicals from Stachytarpheta cayennensis (Verbenaceae) against Gramnegative multidrugresistant phenotypes expressing efux pumps. Invest Med Chem Pharmacol. 3(1):1–9. doi: 10.31183/imcp.2020.00035.
   Google Scholar