Chemical Compound

J3.543.145D

J3.543.145D chemical structure
Primary Record

J3.543.145D

In stock
550 g
Purity
98.1 %

Compound Identifiers & Properties

PubChem CID
177589595
SMILES
B1(C2=C(CO1)C=CC(=C2)S(=O)(=O)N[C@H]3[C@@H]([C@H](O[C@H]([C@H]3O)O[C@@H]4C[C@H]5[C@@H]([C@H](C[C@](O5)(C[C@H](C[C@H]([C@@H](CC[C@H](C[C@H](CC(=O)O[C@H]([C@@H]([C@@H]([C@H](C=CC=CC=CC=CC=CC=CC=C4)C)O)C)C)O)O)O)O)O)O)O)C(=O)O)C)O)O
Canonical SMILES
C[C@@H]1[C@H](O)[C@@H](C)C=CC=CC=CC=CC=CC=CC=C[C@H](O[C@@H]2O[C@H](C)[C@@H](O)[C@H](NS(=O)(=O)c3ccc4c(c3)B(O)OC4)[C@@H]2O)C[C@@H]2O[C@](O)(C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)CC(=O)O[C@H]1C)C[C@H](O)[C@H]2C(=O)O

Names & Synonyms

  • J3.543.145D
  • 3-N -[(1-Hydroxy-1,3-dihydro-2,1-benzooxaborol-6-yl)sulfonyl]Amphotericin B ester
  • (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,33R,35S,36R,37S)-33-{[(2R,3S,4S,5S,6R)-3,5-dihydroxy-4-(1-hydroxy-1,3-dihydro-2,1-benzoxaborole-6-sulfonamido)-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-carboxylic acid