BDBM50498844 CHEMBL3629366

SMILES: CC(C)C[C@@H]1N=C(C)c2ccc(cc2NC1=O)C(=O)OC(C)(C)C

InChI Key: InChIKey=VFEQYIFWTMCFSK-INIZCTEOSA-N

Data: 1 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50498844   

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
Protease (Human immunodeficiency virus 1 (HIV-1))	BDBM50498844 (CHEMBL3629366) Show SMILES CC(C)C[C@@H]1N=C(C)c2ccc(cc2NC1=O)C(=O)OC(C)(C)C |r,t:5| Show InChI InChI=1S/C19H26N2O3/c1-11(2)9-16-17(22)21-15-10-13(18(23)24-19(4,5)6)7-8-14(15)12(3)20-16/h7-8,10-11,16H,9H2,1-6H3,(H,21,22)/t16-/m0/s1	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.93E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Inhibition of recombinant HIV-1 protease expressed in Escherichia coli using Arg-Glu (EDANS)-Ser-Gln-Asn-Tyr-Pro-Ile-Val-Gln Lys(DABCYL)-Arg as subst...				Bioorg Med Chem 23: 7095-109 (2015) Article DOI: 10.1016/j.bmc.2015.09.002 BindingDB Entry DOI: 10.7270/Q2JH3Q5T
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