BDBM50013371 Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu::CHEMBL434474

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)[C@H](Cc1ccc(O)cc1)NC(C)=O)C(C)C)C(C)C)C(O)=O

InChI Key: InChIKey=QLIRUYCHLNQTRS-HWGWDCSQSA-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 = 50013371   

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...)	BDBM50013371 (Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu | CHEMBL434...) 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)[C@H](Cc1ccc(O)cc1)NC(C)=O)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C43H66N10O15/c1-19(2)14-30(43(67)68)51-40(64)29(17-33(58)59)49-39(63)28(16-31(44)56)50-41(65)34(20(3)4)53-42(66)35(21(5)6)52-37(61)23(8)46-32(57)18-45-36(60)22(7)47-38(62)27(48-24(9)54)15-25-10-12-26(55)13-11-25/h10-13,19-23,27-30,34-35,55H,14-18H2,1-9H3,(H2,44,56)(H,45,60)(H,46,57)(H,47,62)(H,48,54)(H,49,63)(H,50,65)(H,51,64)(H,52,61)(H,53,66)(H,58,59)(H,67,68)/t22-,23-,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	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Notre-Dame Hospital Research Curated by ChEMBL					Assay Description Inhibitory activity 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...)	BDBM50013371 (Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu | CHEMBL434...) 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)[C@H](Cc1ccc(O)cc1)NC(C)=O)C(C)C)C(C)C)C(O)=O Show InChI InChI=1S/C43H66N10O15/c1-19(2)14-30(43(67)68)51-40(64)29(17-33(58)59)49-39(63)28(16-31(44)56)50-41(65)34(20(3)4)53-42(66)35(21(5)6)52-37(61)23(8)46-32(57)18-45-36(60)22(7)47-38(62)27(48-24(9)54)15-25-10-12-26(55)13-11-25/h10-13,19-23,27-30,34-35,55H,14-18H2,1-9H3,(H2,44,56)(H,45,60)(H,46,57)(H,47,62)(H,48,54)(H,49,63)(H,50,65)(H,51,64)(H,52,61)(H,53,66)(H,58,59)(H,67,68)/t22-,23-,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	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