BDBM50013363 CHEMBL351165::Tyr-Ala-Gly-Pro-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]1CCCN1C(=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=WCZQZUFNUUPDEL-PZVXROTRSA-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 = 50013363   

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...)	BDBM50013363 (CHEMBL351165 | Tyr-Ala-Gly-Pro-Val-Val-Asn-Asp-Leu) 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]1CCCN1C(=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/C43H66N10O14/c1-20(2)15-29(43(66)67)50-39(62)28(18-33(57)58)48-38(61)27(17-31(45)55)49-41(64)34(21(3)4)52-42(65)35(22(5)6)51-40(63)30-9-8-14-53(30)32(56)19-46-36(59)23(7)47-37(60)26(44)16-24-10-12-25(54)13-11-24/h10-13,20-23,26-30,34-35,54H,8-9,14-19,44H2,1-7H3,(H2,45,55)(H,46,59)(H,47,60)(H,48,61)(H,49,64)(H,50,62)(H,51,63)(H,52,65)(H,57,58)(H,66,67)/t23-,26-,27-,28-,29-,30-,34-,35-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.80E+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
Ribonucleoside-diphosphate reductase large chain (Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)	BDBM50013363 (CHEMBL351165 | Tyr-Ala-Gly-Pro-Val-Val-Asn-Asp-Leu) 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]1CCCN1C(=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/C43H66N10O14/c1-20(2)15-29(43(66)67)50-39(62)28(18-33(57)58)48-38(61)27(17-31(45)55)49-41(64)34(21(3)4)52-42(65)35(22(5)6)51-40(63)30-9-8-14-53(30)32(56)19-46-36(59)23(7)47-37(60)26(44)16-24-10-12-25(54)13-11-24/h10-13,20-23,26-30,34-35,54H,8-9,14-19,44H2,1-7H3,(H2,45,55)(H,46,59)(H,47,60)(H,48,61)(H,49,64)(H,50,62)(H,51,63)(H,52,65)(H,57,58)(H,66,67)/t23-,26-,27-,28-,29-,30-,34-,35-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.40E+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