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Ciclopirox

Ciclopirox (HOE296b) is a synthetic and orally active antifungal agent that can be used for superficial mycoses reseaech. Ciclopirox olamine has a very broad spectrum of activity and inhibits dermatophytes, yeasts, molds, and many Gram-positive and Gram-negative species pathogenic. Ciclopirox also has anticancer and anti-inflammatory effect[1][2][3].

Product Specifications

CAS Number

[29342-05-0]

Product Name Alternative

HOE296b

UNSPSC

12352005

Hazard Statement

H302

Target

Autophagy; Bacterial; Ferroptosis; Fungal

Type

Reference compound

Related Pathways

Anti-infection; Apoptosis; Autophagy

Applications

COVID-19-immunoregulation

Field of Research

Cancer; Infection; Inflammation/Immunology

Assay Protocol

https://www.medchemexpress.com/Ciclopirox.html

Concentration

10mM

Purity

99.84

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

CC(C=C(C1CCCCC1)N2O)=CC2=O

Molecular Formula

C12H17NO2

Molecular Weight

207.27

Precautions

H302

References & Citations

[1]Niewerth, M., et al., Ciclopirox olamine treatment affects the expression pattern of Candida albicans genes encoding virulence factors, iron metabolism proteins, and drug resistance factors. Antimicrob Agents Chemother, 2003. 47 (6) : p. 1805-17.|[2]Leem, S.H., et al., The possible mechanism of action of ciclopirox olamine in the yeast Saccharomyces cerevisiae. Mol Cells, 2003. 15 (1) : p. 55-61.|[3]Ratnavel, R.C., R.A. Squire, and G.C. Boorman, Clinical efficacies of shampoos containing ciclopirox olamine (1.5%) and ketoconazole (2.0%) in the treatment of seborrhoeic dermatitis. J Dermatolog Treat, 2007. 18 (2) : p. 88-96.|[4]Clement PM, et al. The antifungal drug ciclopirox inhibits deoxyhypusine and proline hydroxylation, endothelial cell growth and angiogenesis in vitro. Int J Cancer. 2002 Aug 1;100 (4) :491-8. |[5]Lu J, et al. Ciclopirox targets cellular bioenergetics and activates ER stress to induce apoptosis in non-small cell lung cancer cells. Cell Commun Signal. 2022 Mar 24;20 (1) :37.|[6]Zhou H, et al. The antitumor activity of the fungicide ciclopirox. Int J Cancer. 2010 Nov 15;127 (10) :2467-77.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

Launched

Citation 01

Cell Death Dis. 2025 May 19;16 (1) :403.|Clin Transl Med. 2022 Aug;12 (8) :e999.|Eur J Pharmacol. 2022 Sep 5:930:175156.|Front Pharmacol. 2021 May 10:12:670224.|J Agric Food Chem. 2025 Aug 13;73 (32) :20385-20395.|Mol Cell Biochem. 2024 May 24.|Mol Neurobiol. 2025 Apr;62 (4) :4055-4075.|Adv Healthc Mater. 2025 Jan 24:e2405085.|Pharmacol Res. 2022 Feb:176:106046.

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