Ciclopirox

Catalog No.: A10213

Ciclopirox

Ciclopirox Chemical Structure

CAS NO. 29342-05-0

Ciclopirox is currently being investigated as an alternative treatment to ketoconazole for seborrhoeic dermatitis as it suppresses growth of the yeast Malassezia furfur.It acts by inhibiting the membrane transfer system by interrupting the Na+ K+ ATPase.

Availability: In stock

Package Price Qty
10 mg

Regular Price: $50.00

Special Price $45.00

25 mg

Regular Price: $80.00

Special Price $72.00

50 mg

Regular Price: $150.00

Special Price $135.00

100 mg

Regular Price: $270.00

Special Price $243.00

10mM * 1mL in DMSO

Regular Price: $69.00

Special Price $62.10

Warning Products are for laboratory research use only. Not for human use. We do not sell to patients.

Biological Activity

Ciclopirox is currently being investigated as an alternative treatment to ketoconazole for seborrhoeic dermatitis as it suppresses growth of the yeast Malassezia furfur.It acts by inhibiting the membrane transfer system by interrupting the Na+ K+ ATPase.
Targets
ATPase
In vitro DMSO 42 mg/mL (202.63 mM)
Water <1 mg/mL (<1 mM)
Ethanol 42 mg/mL (202.63 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 48.24 mL 241.2 mL 482.39 mL
0.5 mM 9.65 mL 48.24 mL 96.48 mL
1 mM 4.82 mL 24.12 mL 48.24 mL
5 mM 0.96 mL 4.82 mL 9.65 mL

*The above data is based on the productmolecular weight 207.3 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Chemical Properties

Catalog Num A10213
Actions N/A
M. Wt 207.3
Formula C12H17NO2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 29342-05-0
Synonyms Batrafen, Loprox, Mycoster, Stieprox, HOE 296b
SMILES CC1=CC(=O)N(C(=C1)C2CCCCC2)O

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