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AI67442

1397-89-3 | Amphotericin b

Packsize Purity Availability Price Discounted Price    Quantity
25mg 85% in stock $40.00 $28.00 -   +
500mg 85% in stock $51.00 $36.00 -   +
1g 85% in stock $76.00 $54.00 -   +
5g 85% in stock $219.00 $154.00 -   +
25g 85% in stock $1,042.00 $729.00 -   +

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Description
Catalog Number: AI67442
Chemical Name: Amphotericin b
CAS Number: 1397-89-3
Molecular Formula: C47H73NO17
Molecular Weight: 924.079
MDL Number: MFCD00877763
SMILES: O[C@@H]1CC[C@@H](O)[C@H](O)C[C@H](O)C[C@]2(O)C[C@H](O)[C@H]([C@@H](O2)C[C@H](/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@@H]([C@H]([C@H]([C@@H](OC(=O)C[C@@H](C1)O)C)C)O)C)O[C@@H]1O[C@H](C)[C@H]([C@@H]([C@@H]1O)N)O)C(=O)O

 

Computed Properties
Complexity: 1670  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 19  
Defined Bond Stereocenter Count: 7  
Heavy Atom Count: 65  
Hydrogen Bond Acceptor Count: 18  
Hydrogen Bond Donor Count: 12  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route 
  • The compound (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-Amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid has significant applications in chemical synthesis. This compound can serve as a key building block in the creation of complex organic molecules due to its unique structure and functional groups. By utilizing this compound in chemical synthesis, researchers can access a wide range of potential derivatives and analogs for further study in drug discovery, materials science, and other fields. The compound's intricate molecular architecture offers opportunities for the development of novel synthetic methodologies and the exploration of new chemical reactions. Its presence in the synthesis process can lead to the creation of diverse molecular scaffolds with tailored properties and functionalities, making it a valuable tool in advancing research and innovation in the field of organic chemistry.
Literature
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