BDBM50366468 CHEMBL1790768

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

InChI Key: InChIKey=FTCVTRWEOQELKR-VARUNMFWSA-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 = 50366468   

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...)	BDBM50366468 (CHEMBL1790768) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O Show InChI InChI=1S/C43H68N10O15/c1-9-21(6)34(41(65)49-27(16-30(45)56)38(62)48-28(17-32(58)59)39(63)50-29(43(67)68)14-19(2)3)53-40(64)33(20(4)5)52-42(66)35(23(8)54)51-31(57)18-46-36(60)22(7)47-37(61)26(44)15-24-10-12-25(55)13-11-24/h10-13,19-23,26-29,33-35,54-55H,9,14-18,44H2,1-8H3,(H2,45,56)(H,46,60)(H,47,61)(H,48,62)(H,49,65)(H,50,63)(H,51,57)(H,52,66)(H,53,64)(H,58,59)(H,67,68)/t21-,22-,23-,26-,27-,28-,29-,33-,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...)	BDBM50366468 (CHEMBL1790768) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O Show InChI InChI=1S/C43H68N10O15/c1-9-21(6)34(41(65)49-27(16-30(45)56)38(62)48-28(17-32(58)59)39(63)50-29(43(67)68)14-19(2)3)53-40(64)33(20(4)5)52-42(66)35(23(8)54)51-31(57)18-46-36(60)22(7)47-37(61)26(44)15-24-10-12-25(55)13-11-24/h10-13,19-23,26-29,33-35,54-55H,9,14-18,44H2,1-8H3,(H2,45,56)(H,46,60)(H,47,61)(H,48,62)(H,49,65)(H,50,63)(H,51,57)(H,52,66)(H,53,64)(H,58,59)(H,67,68)/t21-,22-,23-,26-,27-,28-,29-,33-,34-,35-/m0/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Notre-Dame Hospital Research Curated by ChEMBL					Assay Description Inhibitory activity 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