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Micafungin sodium

Catalog No.
A3606
Inhibitor of β-(1,3)-D-glucan synthesis;fungicide
Grouped product items
SizePriceStock Qty
10mM (in 1mL DMSO)
$165.00
In stock
5mg
$77.00
In stock
10mg
$143.00
In stock
25mg
$286.00
In stock
50mg
$429.00
In stock
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

Micafungin is an antifungal agent [1].
Antifungal medicine is a pharmaceutical fungicide used to treat and prevent mycoses such as athlete's foot, ringworm, candidiasis (thrush), serious systemic infections such as cryptococcal meningitis, and others.
Micafungin is an antifungal agent known to inhibit 1,3-β-D-glucan synthesis in Candida albicans. In 13 out of 18 P. Aeruginosa isolates tested, micafungin significantly reduced biofilm biomass. In all 9 P. Aeruginosa isolates tested, micafungin decreased the expression of ndvB, which encoded the cell wall 1,3-β-D-glucan. Also, it decreased the expression of biofilm encoding genes for alginate and pellicles (algC and pelC, respectively) [1].
In a mouse model of septic A. fumigatus infection, micafungin (0.1 mg/kg) increased the survival rate of mice to 20%. When micafungin (0.1 mg/kg) combination with KB425796-C (32 mg/kg), the survival rate of mice increased to 100% in the 31-day post-infection period. While non-treated mice survived for only 6 days [2].
References:
[1]. Bazzi W, Sabra A, Zahreddine L, et al. The inhibitory effect of micafungin on biofilm formation by Pseudomonas aeruginosa. Biofouling, 2013, 29(8): 909-915.
[2]. Kai H, Yamashita M, Nakamura I, et al. Synergistic antifungal activity of KB425796-C in combination with micafungin against Aspergillus fumigatus and its efficacy in murine infection models. J Antibiot (Tokyo), 2013, 66(8): 479-484.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt1292.26
Cas No.208538-73-2
FormulaC56H70N9NaO23S
SynonymsFK 463;Funguard;Mycamine
Solubility≥64.66 mg/mL in DMSO; insoluble in EtOH; ≥17.5 mg/mL in H2O with gentle warming and ultrasonic
SDFDownload SDF
Canonical SMILESCCCCCOC1=CC=C(C=C1)C2=CC(=NO2)C3=CC=C(C=C3)C(=O)NC4CC(C(NC(=O)C5C(C(CN5C(=O)C(NC(=O)C(NC(=O)C6CC(CN6C(=O)C(NC4=O)C(C)O)O)C(C(C7=CC(=C(C=C7)O)OS(=O)(=O)[O-])O)O)C(CC(=O)N)O)C)O)O)O.[Na+]
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

Fungus experiment [1]:

Fungi

Pseudomonas aeruginosa (P. Aeruginosa)

Preparation method

This compound is soluble in water. 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.

Reaction Conditions

10 mg/mL; 24 hrs

Applications

Micafungin decreased the expression of biofilm encoding genes for alginate and pellicles (algC and pelC, respectively).

Animal experiment [2]:

Animal models

A mouse model of septic Aspergillus fumigatus (A. fumigatus) infection

Dosage form

0.1, 0.32 and 1 mg/kg; s.c.; q.d.

Applications

In a mouse model of septic A. fumigatus infection, Micafungin (0.1 mg/kg) increased the survival rate of mice to 20%. When Micafungin (0.1 mg/kg) was combined with KB425796-C (32 mg/kg), the survival rate of mice increased to 100% in the 31-day post-infection period. For non-treated mice, they survived for only 6 days.

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]. Bazzi W, Sabra A, Zahreddine L, et al. The inhibitory effect of micafungin on biofilm formation by Pseudomonas aeruginosa. Biofouling, 2013, 29(8): 909-915.

[2]. Kai H, Yamashita M, Nakamura I, et al. Synergistic antifungal activity of KB425796-C in combination with micafungin against Aspergillus fumigatus and its efficacy in murine infection models. J Antibiot (Tokyo), 2013, 66(8): 479-484.

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