Chemical Compound

Amphotericin B deriv

Amphotericin B deriv chemical structure
Primary Record

Amphotericin B deriv

In stock
550 g
Purity
98.1 %

Compound Identifiers & Properties

PubChem CID
6476002
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](CC[C@@H]([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)NCCOC)O[C@H]3[C@H]([C@H]([C@@H]([C@H](O3)C)O)N)O
Canonical SMILES
COCCNC(=O)[C@H]1[C@@H]2C[C@@H](O[C@@H]3O[C@H](C)[C@@H](O)[C@H](N)[C@@H]3O)/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)[C@@H](O)CC[C@H](O)C[C@H](O)C[C@](O)(C[C@@H]1O)O2

Names & Synonyms

  • Amphotericin B deriv
  • AC1O52GB
  • AIDS108025
  • CID6476002
  • (1S,3R,4E,6E,8E,10E,12E,14E,16E,18S,19R,20S,21S,25R,27S,28S,31S,33S,35R,37S,38R)-3-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-19,25,27,28,31,33,35,37-octahydroxy-N-(2-methoxyethyl)-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10,12,14,16-heptaene-38-carboxamide
  • (1S,3R,4E,6E,8E,10E,12E,14E,16E,18S,19R,20S,21S,25R,27S,28S,31S,33S,35R,37S,38R)-3-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,28,31,33,35,37-octahydroxy-N-(2-methoxyethyl)-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10,12,14,16-heptaene-38-carboxamide
  • 14,39-Dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxamide, 33-[(3-amino-3,6-dideoxy-b-D-mannopyranosyl)oxy]-1,3,5,8,9,11,17,37-octahydroxy-N-(2-methoxyethyl)-15,16,18-trimethyl-13-oxo-, (1R,3S,5S,8S,9S,11R,15S,16S,17R,18S,33R,35S,36R,37S)