Chemical Compound

AC1LAD3E

AC1LAD3E chemical structure
Primary Record

AC1LAD3E

In stock
550 g
Purity
98.1 %

Compound Identifiers & Properties

PubChem CID
466179
SMILES
CC(C)C(C(=O)N[C@@H](CC1=CC=CC=C1)[C@@H]([C@H]([C@H](CC2=CC=CC=C2)NC(=O)C(C(C)C)NC(=O)N3CCOCC3)O)O)NC(=O)N4CCOCC4
Canonical SMILES
CC(C)C(NC(=O)N1CCOCC1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)N1CCOCC1)C(C)C

Names & Synonyms

  • AC1LAD3E
  • AIDS045730
  • CID466179
  • Diol-based HIV Protease inhibitor Derivative
  • N-[1-[[(1S,2S,3S,4S)-1-benzyl-2,3-dihydroxy-4-[[3-methyl-2-(morpholine-4-carbonylamino)butanoyl]amino]-5-phenyl-pentyl]carbamoyl]-2-methyl-propyl]morpholine-4-carboxamide
  • N-[1-[[(2S,3S,4S,5S)-3,4-dihydroxy-5-[[3-methyl-2-(morpholine-4-carbonylamino)butanoyl]amino]-1,6-diphenylhexan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]morpholine-4-carboxamide
  • N-{(1S,2S,3S,4S)-2,3-Dihydroxy-4-[3-methyl-2-(morpholin-4-ylcarbonylamino)butanoylamino]-5-phenyl-1-benzylpentyl}-3-methyl-2-(morpholin-4-ylcarbonylamino)butanamidexy-9,17-dioxo-13,14,15-tris(3,4,5-trihydroxyphenylcarbonyloxy)(10,11,13,14,15,16,11a,15a-octahydro-11aH-dibenzo[a,c]pyrano[3,2-g][11]annulen-2-yloxy)]benzoate