A coumarin with an unusual structure from Cuphea ignea, its cytotoxicity and antioxidant activities

Show simple item record

dc.contributor.author Moustafa E.S.
dc.contributor.author Swilam N.F.
dc.contributor.author Ghanem O.B.
dc.contributor.author Hashim A.N.
dc.contributor.author Nawwar M.A.
dc.contributor.author Lindequist U.
dc.contributor.author Linscheid M.W.
dc.contributor.other October University for Modern Sciences and Arts
dc.contributor.other 6th October City
dc.contributor.other Egypt; Pharmacognosy Department
dc.contributor.other Faculty of Pharmacy
dc.contributor.other British University
dc.contributor.other Egypt; Under Graduate Research Trainee
dc.contributor.other Faculty of Pharmacy
dc.contributor.other German University
dc.contributor.other Cairo
dc.contributor.other Egypt; Department of Phytochemistry and Plant Systematics
dc.contributor.other National Research Center
dc.contributor.other 14 El Tahrier Str.
dc.contributor.other Dokki
dc.contributor.other Cairo
dc.contributor.other 1361
dc.contributor.other Egypt; Pharmaceutical Biology
dc.contributor.other Institute of Pharmacy
dc.contributor.other Ernst-Moritz-Arndt-University
dc.contributor.other Greifswald
dc.contributor.other Germany; Laboratory of Applied Analytical and Environmental Chemistry
dc.contributor.other Humboldt-University
dc.contributor.other Berlin
dc.contributor.other Germany
dc.date.accessioned 2020-01-09T20:41:10Z
dc.date.available 2020-01-09T20:41:10Z
dc.date.issued 2018
dc.identifier.issn 317144
dc.identifier.other https://doi.org/10.1691/ph.2018.7946
dc.identifier.other PubMed ID 29609693
dc.identifier.uri https://t.ly/ZvH2
dc.description Scopus
dc.description.abstract Phenolic metabolite profiling using two dimensional paper chromatographic analysis (2 DPC) was used for assaying the complex mixture of phenolics of an aqueous ethanol aerial part extract of Cuphea ignea (Lytheraceae). A coumarin with a rare structure, namely, 7-hydroxy 3-methoxy coumarin 5-O-?-glucopyranoside was isolated from the investigated extract. The structure was elucidated by conventional methods and spectral analysis, including one and two dimensional NMR (1D and 2D NMR), as well as by interpretation of the spectra obtained by high resolution electrospray ionization mass technique (HRESIMS). The rare coumarin significantly inhibited reactive oxygen species production with an ED50 value of 6.31�1.64 ?g/ml and 5.78�0.66 ?g/ml as determined by the the free radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) and the oxygen radical absorption capacity (ORAC) assay respectively. The isolated coumarin presented a cytotoxic activity assessed by using the neutral red assay (NRU) against lung cancer cell line (H23) with IC50 of 40.38�2.75 ?g/ml. � 2018 Govi-Verlag Pharmazeutischer Verlag GmbH. All rights reserved. en_US
dc.description.uri https://www.scimagojr.com/journalsearch.php?q=21717&tip=sid&clean=0
dc.language.iso English en_US
dc.publisher Govi-Verlag Pharmazeutischer Verlag GmbH en_US
dc.relation.ispartofseries Pharmazie
dc.relation.ispartofseries 73
dc.subject 7 hydroxy 3 methoxycoumarin 5 o beta glucopyranoside en_US
dc.subject coumarin derivative en_US
dc.subject Cuphea ignea extract en_US
dc.subject etoposide en_US
dc.subject plant extract en_US
dc.subject reactive oxygen metabolite en_US
dc.subject unclassified drug en_US
dc.subject 1,1-diphenyl-2-picrylhydrazyl en_US
dc.subject antineoplastic agent en_US
dc.subject antioxidant en_US
dc.subject biphenyl derivative en_US
dc.subject coumarin derivative en_US
dc.subject picric acid en_US
dc.subject plant extract en_US
dc.subject reactive oxygen metabolite en_US
dc.subject scavenger en_US
dc.subject antioxidant activity en_US
dc.subject Article en_US
dc.subject cell viability en_US
dc.subject controlled study en_US
dc.subject Cuphea en_US
dc.subject Cuphea ignea en_US
dc.subject DPPH radical scavenging assay en_US
dc.subject drug cytotoxicity en_US
dc.subject drug identification en_US
dc.subject drug isolation en_US
dc.subject drug structure en_US
dc.subject ED50 en_US
dc.subject HaCat cell line en_US
dc.subject HCT 116 cell line en_US
dc.subject Huh-7 cell line en_US
dc.subject human en_US
dc.subject human cell en_US
dc.subject IC50 en_US
dc.subject NCI-H23 cell line en_US
dc.subject NCI-H460 cell line en_US
dc.subject ORAC assay en_US
dc.subject cell survival en_US
dc.subject chemistry en_US
dc.subject drug effect en_US
dc.subject electrospray mass spectrometry en_US
dc.subject flower en_US
dc.subject metabolism en_US
dc.subject nuclear magnetic resonance spectroscopy en_US
dc.subject tumor cell line en_US
dc.subject Antineoplastic Agents, Phytogenic en_US
dc.subject Antioxidants en_US
dc.subject Biphenyl Compounds en_US
dc.subject Cell Line, Tumor en_US
dc.subject Cell Survival en_US
dc.subject Coumarins en_US
dc.subject Cuphea en_US
dc.subject Flowers en_US
dc.subject Free Radical Scavengers en_US
dc.subject Humans en_US
dc.subject Magnetic Resonance Spectroscopy en_US
dc.subject Picrates en_US
dc.subject Plant Extracts en_US
dc.subject Reactive Oxygen Species en_US
dc.subject Spectrometry, Mass, Electrospray Ionization en_US
dc.title A coumarin with an unusual structure from Cuphea ignea, its cytotoxicity and antioxidant activities en_US
dc.type Article en_US
dcterms.isReferencedBy Brand-Williams, W., Cuvelier, M., Use of a free radical method to evaluate antioxidant activity (1995) Food Sci and Technol, 28, pp. 25-30; (2013) Cuphea Ignea, , Royal Horticultural Society, Retrieved 22 July; Garcia-Granados, A., Buruage, J.M.S., The 13C NMR spectrum of 5-O-?-D-primeverosyl genkwanine (1980) Org Magn Reson, 13, p. 462; Hussein, S., Hashim, A.N., Barakat, H.H., Jose, J., Lindequist, U., Mam, N., Phenolics from extracts of Brahea armata with inhibitory effect against 5?-reductase type-II (2006) Pharmazie, 61, pp. 1034-1037; Lindl, T., Bauer, J., (1989) Zell- und Gewebekultur, p. 181. , Gustav-Fischer-Verlag Jena; Lucas-Abellan, C., Mercader-Ros, T., Zafrila, M.P., Fortea, M.I., Gabaldon, J.A., Nunez-Delicado, E., ORAC-fluorescein assay to determine the oxygen radical absorbance capacity of resveratrol complexed in cyclodextrins (2008) J Agricult Food Chem, 56, pp. 2254-2259; Nawwar, M.A.M., Marzouk, M.S., Nigge, W., Linscheid, M., High-performance liquid chromatographic/electrospray ionization mass spectrometric screening for polyphenolic compounds of Epilobium hirsutum-The structure of the unique ellagitannin epilobamide-A (1997) J Mass Spectrom, 32, pp. 645-654; Nawwar, M.A.M., Ayoub, N.A., El-Rai, M.A., Bassyouny, F., Mostafa, E.M., Al-Abd, A., Harms, M., Linscheid, W.M., Cytotoxic ellagitannins from Reaumuria vermiculata (2012) Fitoterapia, 83, pp. 1256-1266; Rafie, H.A., El-Tawil, B.A., The electronic absorption spectra of some coumarins. A molecular orbital treatment (1985) Can J Chem, 63, pp. 1173-1179; Venugopala, K.N., Rashmi, V., Odhav, B., (2013) BioMed Research International Review on Natural Coumarin Lead Compounds for Their Pharmacological Activity, , Article ID 963248; Wagner, H., Biochemistry of plant phenolics (1979) Recent Advances in Phytochemistry, 12. , In: Swain T, Harborne JB, Van Sumere CF (eds) , Plenum Press, London
dcterms.source Scopus
dc.identifier.doi https://doi.org/10.1691/ph.2018.7946
dc.identifier.doi PubMed ID 29609693
dc.Affiliation October University for modern sciences and Arts (MSA)


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search MSAR


Advanced Search

Browse

My Account