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Nystatin

Catalog No. T1678   CAS 1400-61-9
Synonyms: Stamycin, Fungicidin, Nystavescent

Nystatin (Fungicidin) is a topical and oral antifungal agent with activity against many species of yeast and candida albicans, which is used largely to treat skin and oropharyngeal candidiasis.

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Nystatin Chemical Structure
Nystatin, CAS 1400-61-9
Pack Size Availability Price/USD Quantity
500 mg In stock $ 39.00
1 mL * 10 mM (in DMSO) In stock $ 39.00
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Purity: 99.36%
Purity: 69.55%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Nystatin (Fungicidin) is a topical and oral antifungal agent with activity against many species of yeast and candida albicans, which is used largely to treat skin and oropharyngeal candidiasis.
In vivo Nystatin combined with endostatin selectively enhances endostatin uptake and biodistribution in tumor blood vessels and tumor tissues rather than in normal tissues of tumor-bearing mice, ultimately leading to elevated antiangiogenic and antitumor efficacies of endostatin in vivo[3]. Liposomal Nystatin, at doses as low as 2 mg/kg of body weight/day, protects neutropenic mice against Aspergillus-induced death in a statistically significant manner at the 50-day time point compared to either the no-treatment, the saline, or the empty-liposome group[4].
Synonyms Stamycin, Fungicidin, Nystavescent
Molecular Weight 926.1
Formula C47H75NO17
CAS No. 1400-61-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 50 mg/mL (53.99 mM)

TargetMolReferences and Literature

1. Ellepola AN, et al. Adhesion of oral Candida species to human buccal epithelial cells following brief exposure to nystatin. Oral Microbiol Immunol. 1999 Dec;14(6):358-63. 2. Haas M, et al. Na-K-Cl cotransport in nystatin-treated tracheal cells: regulation by isoproterenol, apical UTP, and [Cl]i. Am J Physiol. 1994 May;266(5 Pt 1):C1440-52. 3. Chen Y, et al. Cholesterol sequestration by nystatin enhances the uptake and activity of endostatin in endothelium via regulating distinct endocytic pathways. Blood. 2011 Jun 9;117(23):6392-403. 4. Wallace TL, et al. Activity of liposomal nystatin against disseminated Aspergillus fumigatus infection in neutropenic mice. Antimicrob Agents Chemother. 1997 Oct;41(10):2238-43. 5. Li X, Tang H, Huang X, et al. Rigidity‐Dependent Placental Cells Uptake of Silk‐Based Microcapsules[J]. Macromolecular bioscience. 2019: 1900105. 6. Wei Y, Ma L, Zhang L, et al. Noncovalent interaction-assisted drug delivery system with highly efficient uptake and release of paclitaxel for anticancer therapy[J]. International journal of nanomedicine. 2017 Sep 25;12:7039-7051.

TargetMolCitations

1. Qin S, Wang X, Han P, et al. LRP1-Mediated Endocytosis May Be the Main Reason for the Difference in Cytotoxicity of Curcin and Curcin C on U2OS Osteosarcoma Cells. Toxins. 2022, 14(11): 771. 2. Wei Y, Ma L, Zhang L, et al. Noncovalent interaction-assisted drug delivery system with highly efficient uptake and release of paclitaxel for anticancer therapy. International journal of nanomedicine. 2017 Sep 25;12:7039-7051. 3. Li X, Tang H, Huang X, et al. Rigidity‐Dependent Placental Cells Uptake of Silk‐Based Microcapsules. Macromolecular bioscience. 2019: 1900105. 4. Yang C, Xu H, Yang D, et al.A renal YY1-KIM1-DR5 axis regulates the progression of acute kidney injury.Nature Communications.2023, 14(1): 4261.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library FDA-Approved Drug Library Bioactive Compounds Library Max Bioactive Compound Library FDA-Approved & Pharmacopeia Drug Library Approved Drug Library Macrocyclic Compound Library

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Keywords

Nystatin 1400-61-9 Apoptosis Microbiology/Virology Antibiotic Antifungal Fungal Inhibitor inhibit Stamycin Fungicidin Nystavescent inhibitor

 

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