BDBM50013349 Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu-NH2::CHEMBL434089

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(N)=O

InChI Key: InChIKey=GWJHMBLTZWWMLS-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 = 50013349   

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...)	BDBM50013349 (Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu-NH2 | CHEMB...) 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(N)=O Show InChI InChI=1S/C43H67N11O14/c1-19(2)14-27(36(45)61)50-41(66)30(17-33(59)60)51-40(65)29(16-31(44)57)52-42(67)34(20(3)4)54-43(68)35(21(5)6)53-38(63)23(8)47-32(58)18-46-37(62)22(7)48-39(64)28(49-24(9)55)15-25-10-12-26(56)13-11-25/h10-13,19-23,27-30,34-35,56H,14-18H2,1-9H3,(H2,44,57)(H2,45,61)(H,46,62)(H,47,58)(H,48,64)(H,49,55)(H,50,66)(H,51,65)(H,52,67)(H,53,63)(H,54,68)(H,59,60)/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
Ribonucleoside-diphosphate reductase large chain (Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)	BDBM50013349 (Ac-Tyr-Ala-Gly-Ala-Val-Val-Asn-Asp-Leu-NH2 | CHEMB...) 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(N)=O Show InChI InChI=1S/C43H67N11O14/c1-19(2)14-27(36(45)61)50-41(66)30(17-33(59)60)51-40(65)29(16-31(44)57)52-42(67)34(20(3)4)54-43(68)35(21(5)6)53-38(63)23(8)47-32(58)18-46-37(62)22(7)48-39(64)28(49-24(9)55)15-25-10-12-26(56)13-11-25/h10-13,19-23,27-30,34-35,56H,14-18H2,1-9H3,(H2,44,57)(H2,45,61)(H,46,62)(H,47,58)(H,48,64)(H,49,55)(H,50,66)(H,51,65)(H,52,67)(H,53,63)(H,54,68)(H,59,60)/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	7.60E+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