BDBM580965 (4S,4′S,7S,7′S,9aS,9a′S)N,N′-((1S,1′S,2R,2′R)-((1,4-phenylenebis(methylene))bis(oxy))bis(2,3-dihydro-1H-indene-2,1-diyl))bis(8,8-dimethyl-4-((S)-2-(methylamino)propanamido)-5-oxooctahydropyrrolo[2,1-b][1,3]thiazepine-7-carboxamide)::US11492361, Example 22
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]1[C@@H](Cc2ccccc12)OCc1ccc(CO[C@@H]2Cc3ccccc3[C@@H]2NC(=O)[C@H]2N3[C@H](CC2(C)C)SCC[C@H](NC(=O)[C@H](C)NC)C3=O)cc1
InChI Key InChIKey=XOMLETYUTHACON-UHFFFAOYSA-N
Data 1 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 580965
Affinity DataEC50: 8.80nMAssay 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
