BDBM50013345 CHEMBL423453::desamino-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu

SMILES: CC(C)C[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](C)NC(=O)CCc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O

InChI Key: InChIKey=CDJFQDAIUFBXAV-HPBXGNKISA-N

Data: 2 IC50

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 2 hits for monomerid = 50013345   

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
Ribonucleoside-diphosphate reductase large chain (Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)	BDBM50013345 (CHEMBL423453 | desamino-Tyr-Ala-Gly-Ala-Val-Val-As...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](C)NC(=O)CCc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C41H63N9O14/c1-19(2)15-28(41(63)64)48-38(60)27(17-32(55)56)46-37(59)26(16-29(42)52)47-39(61)33(20(3)4)50-40(62)34(21(5)6)49-36(58)23(8)45-31(54)18-43-35(57)22(7)44-30(53)14-11-24-9-12-25(51)13-10-24/h9-10,12-13,19-23,26-28,33-34,51H,11,14-18H2,1-8H3,(H2,42,52)(H,43,57)(H,44,53)(H,45,54)(H,46,59)(H,47,61)(H,48,60)(H,49,58)(H,50,62)(H,55,56)(H,63,64)/t22-,23-,26-,27-,28-,33-,34-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Notre-Dame Hospital Research Curated by ChEMBL					Assay Description Inhibitory activity was determined against HSV-1 Ribonucleoside diphosphate reductase				J Med Chem 33: 723-30 (1990) BindingDB Entry DOI: 10.7270/Q2XD128X
					More data for this Ligand-Target Pair
Ribonucleoside-diphosphate reductase large chain (Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)	BDBM50013345 (CHEMBL423453 | desamino-Tyr-Ala-Gly-Ala-Val-Val-As...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](C)NC(=O)CCc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C41H63N9O14/c1-19(2)15-28(41(63)64)48-38(60)27(17-32(55)56)46-37(59)26(16-29(42)52)47-39(61)33(20(3)4)50-40(62)34(21(5)6)49-36(58)23(8)45-31(54)18-43-35(57)22(7)44-30(53)14-11-24-9-12-25(51)13-10-24/h9-10,12-13,19-23,26-28,33-34,51H,11,14-18H2,1-8H3,(H2,42,52)(H,43,57)(H,44,53)(H,45,54)(H,46,59)(H,47,61)(H,48,60)(H,49,58)(H,50,62)(H,55,56)(H,63,64)/t22-,23-,26-,27-,28-,33-,34-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Notre-Dame Hospital Research Curated by ChEMBL					Assay Description Inhibitory activity against HSV-1 Ribonucleoside diphosphate reductase was determined				J Med Chem 33: 723-30 (1990) BindingDB Entry DOI: 10.7270/Q2XD128X
					More data for this Ligand-Target Pair