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ruthenium(II)-curcumin

Development stage
Preclinical
Lead developer
University of Camerino
Modality
DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Light/Condition-Responsive Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules
01

Overview

**Ruthenium(II)-curcumin** is an organometallic compound consisting of a ruthenium(II) ion complexed with curcumin, designed primarily for **anticancer** applications. It is a member of the class of ruthenium-based metallodrugs that seek to combine the favorable pharmacological properties of curcumin (a natural polyphenolic compound with known antioxidant, anti-inflammatory, and anti-tumor activities) with the promising anticancer profile of ruthenium(II) complexes. Ruthenium(II)-curcumin complexes exhibit significant **cytotoxicity and selectivity toward cancer cells**, particularly against cisplatin-resistant cancer cells, and show reduced toxicity toward non-tumorigenic cells[1][2][3][5]. Mechanistically, these complexes induce cancer cell death by several pathways, including activation of **p53** (wild-type or mutant), induction of **oxidative stress**, modulation of the **NRF2** pathway (nuclear factor erythroid 2-related factor 2), and inhibition of proteasome function and PCNA expression, depending on the specific complex[2][4][5]. They are under preclinical investigation and have not yet reached clinical development or approval.

Other names
ruthenium(II)-curcuminRuCURruthenium(II)-curcumin complex
02

Targets

DNA26S proteasomeNFE2L2 (Nuclear factor (erythroid-derived 2)-like 2)TP53 family

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