1. Anti-infection Apoptosis
  2. Fungal Ferroptosis Bacterial
  3. Ciclopirox olamine

Ciclopirox olamine  (Synonyms: Ciclopirox ethanolamine; HOE 296)

Cat. No.: HY-B0450AG
Handling Instructions

Ciclopirox (olamine) (GMP) is Ciclopirox olamine (HY-B0450A) produced by using GMP guidelines. GMP small molecules work appropriately as an auxiliary reagent for cell therapy manufacture. Ciclopirox (HOE296b) is a synthetic 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.

For research use only. We do not sell to patients.

Ciclopirox olamine Chemical Structure

Ciclopirox olamine Chemical Structure

CAS No. : 41621-49-2

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Description

Ciclopirox (olamine) (GMP) is Ciclopirox olamine (HY-B0450A) produced by using GMP guidelines. GMP small molecules work appropriately as an auxiliary reagent for cell therapy manufacture. Ciclopirox (HOE296b) is a synthetic 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[1].

In Vitro

In a study conducted to further elucidate Ciclopirox GMP's mechanism, several Saccharomyces cerevisiae mutants were screened and tested. Results from interpretation of the effects of both the drug treatment and mutation suggested that Ciclopirox GMP may exert its effect by disrupting DNA repair, cell division signals and structures (mitotic spindles) as well as some elements of intracellular transport[2].
Ciclopirox GMP is a broad-spectrum antifungal with anti-inflammatory properties effective against the yeast implicated in seborrhoeic dermatitis, Malassezia spp[3].
Ciclopirox (olamine) (0.9 μM, 24 h) protects human iPSC-derived RPE cells exposed to TBHP-induced cell from oxidative damage[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[2]

Cell Line: iPSC-derived RPE cells
Concentration: 0.9 μM
Incubation Time: 24 h
Result: Protected human iPSC-derived RPE cells exposed to TBHP-induced cell death.

Real Time qPCR[2]

Cell Line: iPSC-derived RPE cells
Concentration: 0.9 μM
Incubation Time: 24 h
Result: Expressed RPE markers (RPE65, BEST1, MITF).
Molecular Weight

268.35

Formula

C14H24N2O3

CAS No.
SMILES

O=C1C=C(C)C=C(C2CCCCC2)N1O.NCCO

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Ciclopirox olamine Related Classifications

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The dilution calculator equation

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Ciclopirox olamine
Cat. No.:
HY-B0450AG
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