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Recent Development of Transition Metal Complexes as Chemotherapeutic Hypoxia Activated Prodrug (HAP).
- Source :
-
ChemMedChem [ChemMedChem] 2024 Jul 15; Vol. 19 (14), pp. e202400127. Date of Electronic Publication: 2024 Jun 03. - Publication Year :
- 2024
-
Abstract
- Hypoxia is a state characterized by low concentration of Oxygen. Hypoxic state is often found in the central region of solid tumors. Hypoxia is associated with abnormal neovascularization resulted in poor blood flow in tissues and increased proliferation of tumor cells, imbalance between O <subscript>2</subscript> supply and O <subscript>2</subscript> consumption in tumor cells, high concentration of proton and strong reducibility. And, these abnormalities enhance the survival potency of the hypoxic tumours and increase the resistance towards chemotherapy and radiotherapy. One of the approach for treating hypoxic region of tumour is to use reducing environment of hypoxic tumours for reducing a molecule (hypoxia activated prodrug, HAP) and as a result the active drug will be released in hypoxic region in a controlled manner from the prodrug and kill the hypoxic tumour. Co(III) and Pt(IV) complexes with monodentate active drug molecule in the axial position can be reduced to Co(II) and Pt(II) moieties and as a result, the axial ligands (active drug) could come out from the metal center and could show its anticancer activity. In this review we have highlighted the research articles where transition metal-based complexes are used as chemotherapeutic hypoxia activated prodrug molecules which are reported in last 5 years.<br /> (© 2024 Wiley-VCH GmbH.)
- Subjects :
- Humans
Transition Elements chemistry
Neoplasms drug therapy
Cell Proliferation drug effects
Molecular Structure
Drug Screening Assays, Antitumor
Animals
Prodrugs chemistry
Prodrugs pharmacology
Prodrugs chemical synthesis
Prodrugs metabolism
Coordination Complexes chemistry
Coordination Complexes pharmacology
Coordination Complexes chemical synthesis
Antineoplastic Agents chemistry
Antineoplastic Agents pharmacology
Antineoplastic Agents chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1860-7187
- Volume :
- 19
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- ChemMedChem
- Publication Type :
- Academic Journal
- Accession number :
- 38634306
- Full Text :
- https://doi.org/10.1002/cmdc.202400127