Issue 9, 2019

Ferrocene-appended pharmacophores: an exciting approach for modulating the biological potential of organic scaffolds

Abstract

Two exemplary contributions of organometallics in medicinal chemistry, ferroquine and ferrocifen, which exhibit excellent anti-plasmodial and anti-cancer activities, respectively, have opened a new field called medicinal organometallic chemistry. This field has been gaining significant interest due to the recent upsurge in ferrocene-linked organic frameworks with promising biological potential. The success of ferrocene is due to the sustained efforts by organic medicinal chemists and its inherent stability in air, heat and light, low toxicity, low cost and reversible redox properties. The replacement of the aryl/heteroaryl core with a ferrocene nucleus in organic molecules imparts a significant change not only in their molecular properties, such as solubility and hydro-/lipophilicity, but also improves the activities of bioactive compounds. Ferrocifen (ferrocene analogue of hydroxytamoxifen) possesses the remarkable feature of being anti-proliferative against both the MCF-7 (hormone dependent) and MDA-MB-231 (hormone independent) breast cancer cell lines. Accordingly, this review article is aimed at updating researchers on the recent developments (2014–18) on the synthesis and evaluation of ferrocene-containing bio-active pharmacophores with emphasis on their structure–activity relationship and mechanism of action.

Graphical abstract: Ferrocene-appended pharmacophores: an exciting approach for modulating the biological potential of organic scaffolds

Associated articles

Article information

Article type
Perspective
Submitted
23 aug 2018
Accepted
02 jan 2019
First published
02 jan 2019

Dalton Trans., 2019,48, 2840-2860

Ferrocene-appended pharmacophores: an exciting approach for modulating the biological potential of organic scaffolds

A. Singh, I. Lumb, V. Mehra and V. Kumar, Dalton Trans., 2019, 48, 2840 DOI: 10.1039/C8DT03440K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements