BDBM580999 (4S,4′S,7S,7′S,9aS,9a′S)N,N′-((1S,1′S)-((naphthalene-2,7-diylbis(methylene))bis(oxy))bis(1-phenylethane-2,1-diyl))bis(8,8-dimethyl-4-((S)-2-(methylamino)propanamido)-5-oxooctahydropyrrolo[2,1-b][1,3]thiazepine-7-carboxamide)::US11492361, Example 56
SMILES CN[C@@H](C)C(=O)N[C@H]1CCS[C@H]2CC(C)(C)[C@H](N2C1=O)C(=O)N[C@H](COCc1ccc2ccc(COC[C@@H](NC(=O)[C@H]3N4[C@H](CC3(C)C)SCC[C@H](NC(=O)[C@H](C)NC)C4=O)c3ccccc3)cc2c1)c1ccccc1
InChI Key InChIKey=IJMJGUCRLVNUSJ-UHFFFAOYSA-N
Data 1 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 580999
Affinity DataEC50: 2.90nMAssay Description:Jurkat HIV-luciferase clones were maintained in RPMI medium 1640 (Gibco by Life Technologies) containing 10% (vol/vol) fetal bovine serum (SAFC/Sigma...More data for this Ligand-Target Pair