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Butenafine HCl

Catalog No.
B1901
synthetic benzylamine antifungal
Grouped product items
SizePriceStock Qty
10mM (in 1mL DMSO)
$55.00
In stock
1g
$94.00
In stock
5g
$314.00
Ship with 10-15 days
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

Worldwide Distributors

Background

Butenafine hydrochloride is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt353.93
Cas No.101827-46-7
FormulaC23H28ClN
Solubilityinsoluble in H2O; ≥17.55 mg/mL in DMSO; ≥23.6 mg/mL in EtOH
Chemical Name1-(4-tert-butylphenyl)-N-methyl-N-(naphthalen-1-ylmethyl)methanamine;hydrochloride
SDFDownload SDF
Canonical SMILESCC(C)(C)C1=CC=C(C=C1)CN(C)CC2=CC=CC3=CC=CC=C32.Cl
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Protocol

Cell experiment [1]:

Cell lines

Dermatophyte fungi, yeasts, bacteria

Preparation method

The solubility of this compound in DMSO is ≥17.55mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

0.03~0.25 μg/mL

Applications

Butenafine showed limited activity against Candida albicans and no activity against Malassezia furfur. Butenafine is not active against the gram-negative bacteria tested.

Animal experiment [1]:

Animal models

Male Hartley strain guinea pigs

Dosage form

1%, once a day

Application

Butenafine has a good effect on dermatophyte, and the treatment effect is better than naftifine, tolnaftate, clotrimazole, and bifonazole. Using butenafine 24 or 48 hours before infection can help prevent experimental T. mentagrophytes infection.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Kokjohn K, Bradley M, Griffiths B, Ghannoum M. Evaluation of in vitro activity of ciclopirox olamine, butenafine HCl and econazole nitrate against dermatophytes, yeasts and bacteria. Int J Dermatol. 2003 Sep;42 Suppl 1:11-7. PubMed PMID: 12895182.

[2]. Arika T, Yokoo M, Hase T, Maeda T, Amemiya K, Yamaguchi H. Effects of butenafine hydrochloride, a new benzylamine derivative, on experimental dermatophytosis in guinea pigs. Antimicrob Agents Chemother. 1990 Nov;34(11):2250-3. PubMed PMID: 2073116; PubMed Central PMCID: PMC172031.

Quality Control

Chemical structure

Butenafine HCl