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Framycetin sulfate
Price range: 62 CAD through 350 CAD
Products Details
Product Description
– Framycetin sulfate (Neomycin Sulphate B) belongs to aminoglycoside class of antibiotics that contain two or more aminosugars connected by glycosidic bonds.
Web ID
– T2096
Storage Temperature
– -20℃
Shipping
– Blue Ice
Molecular Formula
– C23H52N6O25S3
Citations
– 1. Li J, Fan Y Y, Wen J, et al. Metal-Enhanced Aggregation-Induced Emission Strategy for the HIV-I RNA-Binding Ligand Assay. Analytical Chemistry. 2022
2. Li J, Fan Y Y, Wen J, et al. Metal-Enhanced Aggregation-Induced Emission Strategy for the HIV‑I RNA-Binding Ligand Assay. Analytical Chemistry. 2022, 94(11): 4695-4702
3. Li J, Fan Y Y, Wang M, et al. A Light-Up Strategy with Aggregation-Induced Emission for Identification of HIV-Ι RNA-Binding Small Molecules. Analytical Chemistry,. 2020
References
– Quader, S., Boyd, S., Jenkins, I., & Houston, T. (2007). Multisite Modification of Neomycin B: Combined Mitsunobu and Click Chemistry Approach. The Journal Of Organic Chemistry, 72(6), 1962-1979. doi: 10.1021/jo0620967
CAS Number
– 4146-30-9
Molecular Weight
– C23H52N6O25S3
Compound Purity
– 0.9989
SMILES
– OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.[H][C@@]1(O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@@]2([H])O[C@H]2O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@@H](O[C@@]2([H])O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]2N)[C@H]1O
Pathway
– Microbiology/Virology
Product type
– Small Compound
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.
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