Anidulafungin

目录号: A13436

glucan synthase inhibitor

Anidulafungin

Anidulafungin Chemical Structure

CAS NO. 166663-25-8

Anidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.

库存: 现货

规格 价格 数量
10 mg
¥ 500.00
25 mg
¥ 900.00
50 mg
¥ 1,400.00
10mM * 1mL in DMSO
¥ 1,160.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

详情

Anidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.
Targets
glucan synthase
In vitro DMSO 100 mg/mL heating (87.7 mM)
Water <1 mg/mL (<1 mM)
Ethanol 8 mg/mL heating (7.01 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 8.77 mL 43.85 mL 87.7 mL
0.5 mM 1.75 mL 8.77 mL 17.54 mL
1 mM 0.88 mL 4.39 mL 8.77 mL
5 mM 0.18 mL 0.88 mL 1.75 mL

*The above data is based on the productmolecular weight 1140.25. 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.

Technical Details

目录号 A13436
MECHANISM OF ACTION Inhibitor
M. Wt 1140.25
Formula C58H73N7O17
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 166663-25-8
Synonyms N/A
SMILES CCCCCOC1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=C(C=C3)C(=O)N[C@H]4C[C@H]([C@H](NC(=O)[C@@H]5[C@H]([C@H](CN5C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]6C[C@H](CN6C(=O)[C@@H](NC4=O)[C@@H](C)O)O)[C@@H]([C@H](C7=CC=C(C=C7)O)O)O)[C@@H](C)O)C)O)O)O

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