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R Benhida

Explore the profile of R Benhida including associated specialties, affiliations and a list of published articles. Areas
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Articles 7
Citations 38
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Recent Articles
1.
Danouche M, Bounaga A, Oulkhir A, Boulif R, Zeroual Y, Benhida R, et al.
Sci Total Environ . 2023 Nov; 912:168811. PMID: 38030017
Rare Earth Elements (REEs) are indispensable in the growing smart technologies, such as smart phones and electronic devices, renewable energy, new generation of hybrid cars, etc. These elements are naturally...
2.
Ricci F, Carrassa L, Christodoulou M, Passarella D, Michel B, Benhida R, et al.
Comb Chem High Throughput Screen . 2018 Jan; 21(1):50-56. PMID: 29366408
Background: Epithelial ovarian cancer has a poor prognosis, mostly due to its late diagnosis and the development of drug resistance after a first platinum-based regimen. The presence of a specific...
3.
Warnault P, Yasri A, Coisy-Quivy M, Cheve G, Bories C, Fauvel B, et al.
Curr Med Chem . 2013 Feb; 20(16):2043-67. PMID: 23410174
The tyrosine kinase epidermal growth factor receptor (EGFR) has emerged in recent years as a key and validated target of targeted therapies for solid tumors. It plays a central role...
4.
Guianvarch D, Benhida R, Fourrey J, Maurisse R, Sun J
Chem Commun (Camb) . 2002 Sep; (18):1814-5. PMID: 12240328
Thermal denaturation experiments have established that an oligonucleotide incorporating the artificial nucleobase S, does form a stable triplex with a double stranded DNA which exhibits a pyrimidine interruption within the...
5.
Brancale A, McGuigan C, Algain B, SAVY P, Benhida R, Fourrey J, et al.
Bioorg Med Chem Lett . 2001 Sep; 11(18):2507-10. PMID: 11549457
Thieno analogues of the potent and selective furo-pyrimidine anti-VZV nucleoside family are herein reported. The compounds retain full antiviral potency in comparison to the furo parent.
6.
SAVY P, Benhida R, Fourrey J, Maurisse R, Sun J
Bioorg Med Chem Lett . 2000 Oct; 10(20):2287-9. PMID: 11055340
A short route to pyrimidine locked nucleosides has been developed for their incorporation in triplex forming oligonucleotides (TFO). Compared to oligonucleotides built with standard nucleosides, the modified TFOs containing 3'-endo...
7.
Pontikis R, Benhida R, Aubertin A, Grierson D, Monneret C
J Med Chem . 1997 Jun; 40(12):1845-54. PMID: 9191961
A series of 33 N-1 side chain-modified analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (1, HEPT) were synthesized and evaluated for their anti-HIV-1 activity. In particular, the influence of substitution of the terminal hydroxy...