BDBM50013380 CHEMBL349654::Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Val

SMILES: CC(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)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O

InChI Key: InChIKey=OTSHSMSITVKISF-IVUZDODSSA-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 = 50013380   

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...)	BDBM50013380 (CHEMBL349654 | Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Val) Show SMILES CC(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)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C40H62N10O14/c1-17(2)30(38(61)47-25(14-27(42)52)36(59)46-26(15-29(54)55)37(60)50-32(19(5)6)40(63)64)49-39(62)31(18(3)4)48-34(57)21(8)44-28(53)16-43-33(56)20(7)45-35(58)24(41)13-22-9-11-23(51)12-10-22/h9-12,17-21,24-26,30-32,51H,13-16,41H2,1-8H3,(H2,42,52)(H,43,56)(H,44,53)(H,45,58)(H,46,59)(H,47,61)(H,48,57)(H,49,62)(H,50,60)(H,54,55)(H,63,64)/t20-,21-,24-,25-,26-,30-,31-,32-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.46E+5	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...)	BDBM50013380 (CHEMBL349654 | Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Val) Show SMILES CC(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)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C40H62N10O14/c1-17(2)30(38(61)47-25(14-27(42)52)36(59)46-26(15-29(54)55)37(60)50-32(19(5)6)40(63)64)49-39(62)31(18(3)4)48-34(57)21(8)44-28(53)16-43-33(56)20(7)45-35(58)24(41)13-22-9-11-23(51)12-10-22/h9-12,17-21,24-26,30-32,51H,13-16,41H2,1-8H3,(H2,42,52)(H,43,56)(H,44,53)(H,45,58)(H,46,59)(H,47,61)(H,48,57)(H,49,62)(H,50,60)(H,54,55)(H,63,64)/t20-,21-,24-,25-,26-,30-,31-,32-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.50E+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