Amphotericin B Methyl Ester 90percent

• CAT Number: R056009
• CAS Number: 36148-89-7
• Molecular Formula: C48H75NO17
• Molecular Weight: 938.12
• Purity: ≥95%
• Synonyms: Amphotericin B Monomethyl Ester
• Target: HIV
• Storage: Store at -20C
• IUPAC Name: methyl (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]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-carboxylate
• InChI: InChI=1S/C48H75NO17/c1-28-18-16-14-12-10-8-6-7-9-11-13-15-17-19-35(65-47-45(59)42(49)44(58)31(4)64-47)25-39-41(46(60)62-5)38(55)27-48(61,66-39)26-34(52)23-37(54)36(53)21-20-32(50)22-33(51)24-40(56)63-30(3)29(2)43(28)57/h6-19,28-39,41-45,47,50-55,57-59,61H,20-27,49H2,1-5H3/b7-6+,10-8+,11-9+,14-12+,15-13+,18-16+,19-17+/t28-,29-,30-,31+,32+,33+,34-,35-,36+,37+,38-,39-,41+,42-,43+,44+,45-,47-,48+/m0/s1
• InChIKey: UAZIZEMIKKIBCA-TYVGYKFWSA-N
• SMILES: C[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@@H](C[C@H]2[C@@H]([C@H](C[C@](O2)(C[C@H](C[C@H]([C@@H](CC[C@H](C[C@H](CC(=O)O[C@H]([C@@H]([C@@H]1O)C)C)O)O)O)O)O)O)O)C(=O)OC)O[C@H]3[C@H]([C@H]([C@@H]([C@H](O3)C)O)N)O

Amphotericin B Methyl Ester（Cat No.:R056009）is a derivative of Amphotericin B, an antifungal polyene macrolide. This methyl ester modification reduces its hydrophilicity while retaining antifungal activity, making it a valuable tool for studying structure-activity relationships in antifungal compounds. Amphotericin B Methyl Ester disrupts fungal cell membranes by binding to ergosterol, causing pore formation and cell death. It is commonly used in biochemical research to explore membrane interactions and drug delivery systems. Its 90% purity ensures consistency and reliability for experimental and pharmaceutical studies in antifungal drug development.