Chemodex

Micafungin sodium

CHF 75.00
In stock
CDX-M0187-M0055 mgCHF 75.00
CDX-M0187-M02525 mgCHF 299.00
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Product Details
Synonyms Mycamine; Funguard; FK463; 1-[(4R,5R)-4,5-Dihydroxy-N2-[4-[5-[4-(pentyloxy)phenyl]-3-isoxazolyl]benzoyl]-L-ornithine]-4-[(4S)-4-hydroxy-4-[4-hydroxy-3-(sulfooxy)phenyl]-L-threonine]pneumocandin A0 sodium salt
Product Type Chemical
Properties
Formula C56H70N9NaO23S
MW 1292.26
CAS 208538-73-2
RTECS TP7846500
Source/Host Chemicals Semisynthetic
Purity Chemicals ≥97% (HPLC)
Appearance White to beige powder.
Solubility Soluble in DMSO or DMF (both 10mg/ml). Slightly soluble in ethanol, methanol or water (all 1mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key KOOAFHGJVIVFMZ-WZPXRXMFSA-M
Smiles O[C@@H]([C@@H](C)C1)[C@@H](C(N[C@@H]([C@@H](C2)O)O)=O)N1C([C@H]([C@@H](CC(N)=O)O)NC([C@H]([C@@H]([C@H](C(C=C3)=CC(OS([O-])(=O)=O)=C3O)O)O)NC([C@H](C[C@H]4O)N(C4)C([C@H]([C@@H](C)O)NC([C@H]2NC(C(C=C5)=CC=C5C6=NOC(C(C=C7)=CC=C7OCCCCC)=C6)=O)=O)=O)=O)=O)=O.[Na+]
Shipping and Handling
Shipping BLUE ICE
Short Term Storage -20°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Micafungin is a semisynthetic echinocandin antifungal. Micafungin inhibits the enzyme β(1,3)-D-Glucan synthase, consequently 1,3-β-D-glucan synthesis and thereby disturbing the integrity of the fungal cell wall. It has fungicidal activity against virtually all species of Candida, including those resistant to fluconazole, and is fungistatic against Aspergillus spp. The target enzyme does not exist in mammalian systems.

Product References

(1) M. Tomishima, et al.; J. Antibiot. 52, 674 (1999) | (2) R.A. Fromtling; Drugs Today 38, 245 (2002) (Review) | (3) A.J. Carillo-Munoz, et al.; Rev. Esp. Quimioter. 19, 130 (2006) | (4) J.J. Vehreschild & O.A. Cornely; Future Microbiol. 1, 161 (2006) | (5) J.M. Joseph, et al.; Pharmacotherapy 27, 53 (2007) (Review) | (6) N.P. Wiederhold & J.S. Lewis; Expert Opin. Pharmacother. 8, 1155 (2007) (Review) | (7) A.M. Bormann & V.A. Morrison; Drug. Des. Devel. Ther. 3, 295 (2009)

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