null

SMILES: NC(=O)[C@@H]1CCCN1P([O-])(=O)C(Cc1ccccc1)NC(=O)C(F)(F)F

InChI Key: InChIKey=QFJVYDUPRQCEGG-PXYINDEMSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50279829   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50279829 (((S)-2-Carbamoyl-pyrrolidin-1-yl)-[2-phenyl-1-(2,2...) Show SMILES NC(=O)[C@@H]1CCCN1P([O-])(=O)C(Cc1ccccc1)NC(=O)C(F)(F)F Show InChI InChI=1S/C15H19F3N3O4P/c16-15(17,18)14(23)20-12(9-10-5-2-1-3-6-10)26(24,25)21-8-4-7-11(21)13(19)22/h1-3,5-6,11-12H,4,7-9H2,(H2,19,22)(H,20,23)(H,24,25)/p-1/t11-,12?/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article	5.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for its binding affinity against HIV-1 protease				Bioorg Med Chem Lett 1: 653-658 (1991) Article DOI: 10.1016/S0960-894X(01)81171-9 BindingDB Entry DOI: 10.7270/Q2BP038F
					More data for this Ligand-Target Pair
Gag-Pol polyprotein [489-587] (Human immunodeficiency virus type 1)	BDBM50279829 (((S)-2-Carbamoyl-pyrrolidin-1-yl)-[2-phenyl-1-(2,2...) Show SMILES NC(=O)[C@@H]1CCCN1P([O-])(=O)C(Cc1ccccc1)NC(=O)C(F)(F)F Show InChI InChI=1S/C15H19F3N3O4P/c16-15(17,18)14(23)20-12(9-10-5-2-1-3-6-10)26(24,25)21-8-4-7-11(21)13(19)22/h1-3,5-6,11-12H,4,7-9H2,(H2,19,22)(H,20,23)(H,24,25)/p-1/t11-,12?/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article	n/a	n/a	1.21E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity against HIV-1 protease				Bioorg Med Chem Lett 1: 653-658 (1991) Article DOI: 10.1016/S0960-894X(01)81171-9 BindingDB Entry DOI: 10.7270/Q2BP038F
					More data for this Ligand-Target Pair