Literature DB >> 24079182

Biologically active secondary metabolites from Asphodelus microcarpus.

Mohammed M Ghoneim1, Guoyi Ma, Atef A El-Hela, Abd-Elsalam I Mohammad, Saeid Kottob, Sayed El-Ghaly, Stephen J Cutler, Samir A Ross.   

Abstract

Bioassay guided fractionation of the ethanolic extract of Asphodelus microcarpus Salzm.et Vivi (Asphodelaceae) resulted in the isolation of one new metabolite, 1,6-dimethoxy-3-methyl-2-naphthoic acid (1) as well as nine known compounds: asphodelin (2), chrysophanol (3), 8-methoxychrysophanol (4), emodin (5), 2-acetyl-1,8-dimethoxy-3-methylnaphthalene (6), 10-(chrysophanol-7'-yl)-10-hydroxychrysophanol-9-anthrone (7), aloesaponol-III-8-methyl ether (8), ramosin (9) and aestivin (10). The compounds were identified by 1D and 2D NMR and HRESIMS. Compounds 3, 6 and 10 were isolated for the first time from this species. Compounds 3 and 4 showed moderate to weak antileishmanial activity with IC50 values of 14.3 and 35.1 microg/mL, respectively. Compound 4 exhibited moderate antifungal activity against Cryptococcus neoformans with an IC50 value of 15.0 microg/mL, while compounds 5, 7 and 10 showed good to potent activity against methicillin resistant Staphylococcus aureus (MRSA) with IC50 values of 6.6, 9.4 microg/mL and 1.4 microg/mL respectively. Compounds 5, 8 and 9 displayed good activity against S. aureus with IC50 values of 3.2, 7.3 and 8.5 microg/mL, respectively. Compounds 7 and 9 exhibited a potent cytotoxic activity against leukemia LH60 and K562 cell lines. Compound 10 showed potent antimalarial activities against both chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum with IC50 values in the range of 0.8-0.7 microg/mL without showing any cytotoxicity to mammalian cells.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24079182

Source DB:  PubMed          Journal:  Nat Prod Commun        ISSN: 1555-9475            Impact factor:   0.986


  10 in total

1.  Inhibition of cell-intrinsic NF-κB activity and metastatic abilities of breast cancer by aloe-emodin and emodic-acid isolated from Asphodelus microcarpus.

Authors:  Amira A Abdellatef; Moustafa Fathy; Abd El-Salam I Mohammed; Marwa S Abu Bakr; Amal H Ahmed; Hatem S Abbass; Ahmed H El-Desoky; Hiroyuki Morita; Toshio Nikaido; Yoshihiro Hayakawa
Journal:  J Nat Med       Date:  2021-05-14       Impact factor: 2.343

2.  Asphodosides A-E, anti-MRSA metabolites from Asphodelus microcarpus.

Authors:  Mohammed M Ghoneim; Khaled M Elokely; Atef A El-Hela; Abd-Elsalam I Mohammad; Melissa Jacob; Mohamed M Radwan; Robert J Doerksen; Stephen J Cutler; Samir A Ross
Journal:  Phytochemistry       Date:  2014-07-14       Impact factor: 4.072

3.  Isolation and characterization of new secondary metabolites from Asphodelus microcarpus.

Authors:  Mohammed M Ghoneim; Khaled M Elokely; Atef A El-Hela; Abd Elsalam I Mohammad; Melissa Jacob; Stephen J Cutler; Robert J Doerksen; Samir A Ross
Journal:  Med Chem Res       Date:  2014-02-11       Impact factor: 1.965

4.  Anti-Acne Activity of Italian Medicinal Plants Used for Skin Infection.

Authors:  Kate Nelson; James T Lyles; Tracy Li; Alessandro Saitta; Eugenia Addie-Noye; Paula Tyler; Cassandra L Quave
Journal:  Front Pharmacol       Date:  2016-11-10       Impact factor: 5.810

5.  Tyrosinase inhibition and antioxidant properties of Asphodelus microcarpus extracts.

Authors:  Amalia Di Petrillo; Ana Maria González-Paramás; Benedetta Era; Rosaria Medda; Francesca Pintus; Celestino Santos-Buelga; Antonella Fais
Journal:  BMC Complement Altern Med       Date:  2016-11-09       Impact factor: 3.659

6.  Broad-range potential of Asphodelus microcarpus leaves extract for drug development.

Authors:  Amalia Di Petrillo; Antonella Fais; Francesca Pintus; Celestino Santos-Buelga; Ana M González-Paramás; Vincenzo Piras; Germano Orrù; Antonello Mameli; Enzo Tramontano; Aldo Frau
Journal:  BMC Microbiol       Date:  2017-07-14       Impact factor: 3.605

Review 7.  A Comprehensive Review on the Medicinal Plants from the Genus Asphodelus.

Authors:  Maryam Malmir; Rita Serrano; Manuela Caniça; Beatriz Silva-Lima; Olga Silva
Journal:  Plants (Basel)       Date:  2018-03-13

8.  (R)-(-)-Aloesaponol III 8-Methyl Ether from Eremurus persicus: A Novel Compound against Leishmaniosis.

Authors:  Daniela Rossi; Karzan Mahmood Ahmed; Raffaella Gaggeri; Serena Della Volpe; Lauretta Maggi; Giuseppe Mazzeo; Giovanna Longhi; Sergio Abbate; Federica Corana; Emanuela Martino; Marisa Machado; Raquel Varandas; Maria do Céu Sousa; Simona Collina
Journal:  Molecules       Date:  2017-03-24       Impact factor: 4.411

9.  LC-ESI/MS-Phytochemical Profiling with Antioxidant, Antibacterial, Antifungal, Antiviral and In Silico Pharmacological Properties of Algerian Asphodelus tenuifolius (Cav.) Organic Extracts.

Authors:  Ayoub Khalfaoui; Emira Noumi; Soumia Belaabed; Kaïss Aouadi; Bouslama Lamjed; Mohd Adnan; Andrea Defant; Adel Kadri; Mejdi Snoussi; Mushtaq Ahmad Khan; Ines Mancini
Journal:  Antioxidants (Basel)       Date:  2021-04-20

10.  A Cell-Based Metabonomics Approach to Investigate the Varied Influences of Chrysophanol-8-O-β-D-Glucoside With Different Concentrations on L-02 Cells.

Authors:  Meichen Liu; Xiaohong Gong; Yunyun Quan; Yimeng Zhou; Yunxia Li; Cheng Peng
Journal:  Front Pharmacol       Date:  2019-01-09       Impact factor: 5.810

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.