Amgad I.M. Khedr
Port Said University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Amgad I.M. Khedr.
Journal of Asian Natural Products Research | 2018
Sabrin R.M. Ibrahim; Gamal A. Mohamed; Mahmoud Abdelkhalek Elfaky; Rwaida A. Al Haidari; Mohamed F. Zayed; Amal A. El-Kholy; Amgad I.M. Khedr
Abstract A new prenylated xanthone, garcixanthone A (5), together with eight known compounds, mangostanaxanthones I (1) and II (2), garcinone E (3), β-mangostin (4), 8-hydroxycudraxanthone G (6), garcinone C (7), cudraxanthone G (8), and (-)-epicatechin (9) were isolated from the EtOAc-soluble fraction of the air-dried pericarps of Garcinia mangostana (family Clusiaceae). Their structures were verified on the basis of spectroscopic data interpretation as well as comparison with the literature. The cytotoxic and antimicrobial activities of the new compound were assessed using sulforhodamine B (SRB) and agar disk diffusion assays, respectively. Compound 5 showed significant cytotoxic potential against epithelial lung carcinoma (A549) and breast carcinoma (MCF7) cell lines with IC50s 3.0 and 4.2 μM, respectively, compared to doxorubicin (0.74 and 0.41 μM, respectively).
Journal of Asian Natural Products Research | 2018
Sabrin R.M. Ibrahim; Amgad I.M. Khedr; Gamal A. Mohamed; Mohamed F. Zayed; Amal A. El-Kholy; Rwaida A. Al Haidari
Abstract Phytochemical investigation of the methanolic extract of Cucumis melo L. (Cucurbitaceae) seeds furnished a new triterpene benzoate derivative: cucumol B (1) and four known flavonoids: quercetin-3-O-β-D-glucopyranosyl-(1→6)-α-L-rhamnopyranoside (2), quercetin-3-O-β-D-glucopyranoside (3), quercetin (4), and luteolin (5). Their structures were identified by UV, IR, 1D (13C and 1H), 2D (HSQC, 1H-1H COSY, HMBC, and NOESY) NMR, and HRESIMS spectral as well as comparing with literature data. Compound 1 has been assessed for the in vitro cytotoxic effect against SKOV-3, MCF-7, and HCT-116 cell lines. It had selective and potent effect toward SKOV-3 and MCF-7 cell lines with IC50s 2.05 and 0.41 μM, respectively, in comparison to doxorubicin (IC50s 0.32 and 0.05 μM). However, it showed moderate activity toward HCT-116 cell line with IC50 8.27 μM.
Phytochemistry Letters | 2015
Sabrin R.M. Ibrahim; Ehab S. Elkhayat; Gamal A. Mohamed; Amgad I.M. Khedr; Mostafa A. Fouad; Mohamed H.R. Kotb; Samir A. Ross
Archives of Pharmacal Research | 2016
Amgad I.M. Khedr; Sabrin R.M. Ibrahim; Gamal A. Mohamed; Hany E.A. Ahmed; Amany S. Ahmad; Mahmoud A. Ramadan; Atef E. Abd El-Baky; Koji Yamada; Samir A. Ross
Phytochemistry Letters | 2015
Amgad I.M. Khedr; Gamal A. Mohamed; Mohamed A.A. Orabi; Sabrin R.M. Ibrahim; Koji Yamada
Revista Brasileira De Farmacognosia-brazilian Journal of Pharmacognosy | 2017
Sabrin R.M. Ibrahim; Abdulrahman M. Alahdal; Amgad I.M. Khedr; Gamal A. Mohamed
Journal of Pharmacognosy and Phytochemistry | 2015
Amgad I.M. Khedr; Ahamed E. Allam; Alaa M. Nafady; Amany S. Ahmad; Mahmoud A. Ramadan
Phytochemistry Letters | 2018
Amgad I.M. Khedr; Sabrin R.M. Ibrahim; Gamal A. Mohamed; Samir A. Ross; Koji Yamada
Trends in Phytochemical Research | 2018
Ahmed E. Allam; Alaa Mohamed Nafady; Amgad I.M. Khedr; Toshinori Nakagawa; Kuniyoshi Shimizu
Journal of Food Biochemistry | 2018
Sabrin R.M. Ibrahim; Gamal A. Mohamed; Amgad I.M. Khedr; Mohamed F. Zayed; Amal A. El-Kholy