Xanthones: A Class of Heterocyclic Compounds with Anticancer Potential.

Antitumor activity Bioactive compounds Biomedical uses Cancer Pharmacophore Xanthone derivatives

Journal

Current topics in medicinal chemistry
ISSN: 1873-4294
Titre abrégé: Curr Top Med Chem
Pays: United Arab Emirates
ID NLM: 101119673

Informations de publication

Date de publication:
2022
Historique:
received: 16 05 2022
revised: 09 07 2022
accepted: 18 07 2022
pubmed: 4 9 2022
medline: 16 11 2022
entrez: 3 9 2022
Statut: ppublish

Résumé

Xanthones (9H xanthen-9-one) are an important class of heterocyclic compounds containing oxygen and a moiety of gamma-pirone, dense with a two-benzene ring structure, distributed widely in nature. Naturally occurring xanthones are found in micro-organisms and higher plants as secondary metabolites in fungi and lichens. Compounds of the family Caryophyllaceae, Guttiferae and Gentianaceae, are the most common natural source of xanthones. The structure of the xanthones nucleus, coupled with its biogenetic source, imposes that the carbons are numbered according to the biosynthetic pact. The characteristics oxygenation pattern of xanthones earlier is mixed shikimateacetate biogenesis. The major class of xanthones includes simple oxygenated, non-oxygenated, xanthonolignoids, bisxanthones, prenylated and related xanthones, miscellaneous xanthones. Their great pharmacological importance and interesting scaffolds were highly encouraged by scientists to investigate either the synthesis design or natural products for cancer treatment. Because currently used antitumor drugs possess high toxicity and low selectivity, efficacious treatment may be compromised. This review is limited to the antitumor activity of xanthones and the chemistry of xanthone core, which may help provide fundamental knowledge to the medicinal chemist for new and advanced research in drug development.

Identifiants

pubmed: 36056870
pii: CTMC-EPUB-126091
doi: 10.2174/1568026622666220901145002
doi:

Substances chimiques

Xanthones 0
Antineoplastic Agents 0
Biological Products 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1930-1949

Subventions

Organisme : Umm AL-Qura University
ID : 22UQU4250073DSR07

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Somia Gul (S)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jinnah University for Women, Karachi, 74600, Pakistan.

Khadija Aslam (K)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jinnah University for Women, Karachi, 74600, Pakistan.

Quratulain Pirzada (Q)

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jinnah University for Women, Karachi, 74600, Pakistan.

Abdur Rauf (A)

Department of Chemistry, University of Swabi, Swabi, Anbar, 23430, Khyber Pakhtunkhwa (KP), Pakistan.

Anees Ahmed Khalil (AA)

University Institute of Diet and Nutritional Sciences, Faculty of Allied Health Sciences, The University of Lahore, Lahore, Pakistan.

Prabhakar Semwal (P)

Department of Life Sciences, Graphic Era Deemed to be University, Dehradun, Uttarakhand, India.

Sami Bawazeer (S)

Department of Pharmacognosy, Faculty of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.

Yahya Saleh Al-Awthan (YS)

Department of Biology, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Department of Biology, Faculty of Science, Ibb University, Ibb, Yemen.

Omar Salem Bahattab (OS)

Department of Biology, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.

Mohammed Ali Al Duais (MA)

Department of Biochemistry, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Biochemistry Unit, Chemistry Department, Faculty of Science, Ibb University, Ibb, Yemen.

Muthu Thiruvengadam (M)

Department of Crop Science, College of Sanghuh Life Sciences, Konkuk University, Seoul, 05029, Republic of Korea.

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Classifications MeSH