Chemodex

Caspofungin diacetate

CHF 68.00
In stock
CDX-C0267-M0055 mgCHF 68.00
CDX-C0267-M02525 mgCHF 272.00
More Information
Product Details
Synonyms L-743,872; MK 0991
Product Type Chemical
Properties
Formula

C52H88N10O15 . 2C2H4O2

MW 1213.42
CAS 179463-17-3
RTECS TP8046500
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance White to beige powder.
Solubility Soluble in DMSO (25mg/ml), DMF (20mg/ml), ehtanol (20mg/ml) or water (15mg/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 OGUJBRYAAJYXQP-IJFZAWIJSA-N
Smiles OC(C)=O.O=C([C@H]([C@@H](CCN)O)NC([C@H]([C@@H]([C@H](C(C=C1)=CC=C1O)O)O)NC([C@H](C2)N(C[C@@H]2O)C([C@H]([C@@H](C)O)NC([C@@H](NC(CCCCCCCC[C@@H](C)C[C@@H](C)CC)=O)C3)=O)=O)=O)=O)N4[C@@](C(N[C@@H]([C@@H]3O)NCCN)=O)([H])[C@@H](O)CC4.O=C(C)O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°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
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Caspofungin acetate is an antifungal compound that is classified as an echinocandin. It is a semi-synthetic analogue of pneumocandin B0 with improved water solubility, a significant limitation in the development of the echinocandin class as pharmaceuticals. Caspofungin acetate acts by non-competititvely inhibiting the enzyme 1,3-β glucan synthase and preventing the synthesis of glucan and distutbing the integrity in the fungal cell wall. This agent is used in fungal cell wall biosynthesis research to study the role of β-1,3-D-glucans in cell wall integrity and fungal survival under various environmental and chemical stresses. It is effective against disseminated or invasive aspergillosis and candidiasis in mice.

Product References

(1) G.K. Abruzzo, et al.; Antimicrob. Agents Chemother. 41, 2333 (1997) | (2) V. Letscher-Bru, et al.; J. Antimicrob. Chemother. 51, 513 (2003) | (3) S.C. Deresinski & D.A. Stevens; Clin. Infect. Dis. 36, 1445 (2003) | (4) R. Herbrecht, et al.; J. Antimicrob. Chemother. 56, i39 (2005) | (5) M.A. Pfaller, et al.; J. Clin. Microbiol. 47, 3323 (2009) | (6) J.M. Balkovec, et al.; Nat. Prod. Rep. 31, 15 (2014)

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