Novel alloxazine analogues: design, synthesis, and antitumour efficacy enhanced by kinase screening, molecular docking, and ADME studies.


Journal

Journal of enzyme inhibition and medicinal chemistry
ISSN: 1475-6374
Titre abrégé: J Enzyme Inhib Med Chem
Pays: England
ID NLM: 101150203

Informations de publication

Date de publication:
Dec 2024
Historique:
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 17 9 2024
Statut: ppublish

Résumé

This study describes the development of novel alloxazine analogues as potent antitumor agents with enhanced selectivity for tumour cells. Twenty-nine out of 45 newly compounds were investigated

Identifiants

pubmed: 39287132
doi: 10.1080/14756366.2024.2398551
doi:

Substances chimiques

Antineoplastic Agents 0
isoalloxazine 490-59-5
Protein Kinase Inhibitors 0
Flavins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2398551

Auteurs

Doaa Samaha (D)

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Helwan University, Helwan, Egypt.
Institute of Chemistry, Humboldt-Universität zu Berlin, Berlin, Germany.

Sawsan Mahmoud (S)

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Helwan University, Helwan, Egypt.

Mosaad Sayed Mohamed (MS)

Pharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Helwan University, Helwan, Egypt.

Rokaia S Abdullah (RS)

Environment Division, National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt.
Department of Pharmaceutical Sciences, Irma Lerma Rangel School of Pharmacy, Texas A&M University, College Station, TX, USA.

Nageh A Abou Taleb (N)

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Helwan University, Helwan, Egypt.

Tomohisa Nagamatsu (T)

Laboratory of Curative Creation Study for Geriatric-diseases Prevention, Faculty of Pharmacological Sciences, Sojo University, Kumamoto, Japan.

Hamed I Ali (HI)

Department of Pharmaceutical Sciences, Irma Lerma Rangel School of Pharmacy, Texas A&M University, College Station, TX, USA.

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Classifications MeSH