Chemical Compound

AC1LAD3K

AC1LAD3K chemical structure
Primary Record

AC1LAD3K

In stock
550 g
Purity
98.1 %

Compound Identifiers & Properties

PubChem CID
466181
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)N3CCN(CC3)CC4=CC=CC=C4)O)O)NC(=O)N5CCN(CC5)CC6=CC=CC=C6
Canonical SMILES
CC(C)C(NC(=O)N1CCN(Cc2ccccc2)CC1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)N1CCN(Cc2ccccc2)CC1)C(C)C

Names & Synonyms

  • AC1LAD3K
  • AIDS045732
  • CID466181
  • Diol-based HIV Protease inhibitor Derivative
  • 4-benzyl-N-[1-[[(1S,2R,3R,4S)-1-benzyl-4-[[2-[(4-benzylpiperazine-1-carbonyl)amino]-3-methyl-butanoyl]amino]-2,3-dihydroxy-5-phenyl-pentyl]carbamoyl]-2-methyl-propyl]piperazine-1-carboxamide
  • 4-benzyl-N-[1-[[(2S,3R,4R,5S)-5-[[2-[(4-benzylpiperazine-1-carbonyl)amino]-3-methylbutanoyl]amino]-3,4-dihydroxy-1,6-diphenylhexan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]piperazine-1-carboxamide
  • N-[(1S,4S,2R,3R)-2,3-Dihydroxy-4-(3-methyl-2-{[4-benzylpiperazinyl]carbonylamino}butanoylamino)-5-phenyl-1-benzylpentyl]-3-methyl-2-{[4-benzylpiperazinyl]carbonylamino}butanamide