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BDBM50013372 CHEMBL2371373::Tyr-Thr-Met-Leu-Val-Val-Asn-Asp-Leu

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

InChI Key: InChIKey=SOVKPFHAJCTFNJ-HZQKZEJLSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50013372   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Ribonucleoside-diphosphate reductase large chain


(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
BDBM50013372
PNG
(CHEMBL2371373 | Tyr-Thr-Met-Leu-Val-Val-Asn-Asp-Le...)
Show SMILES CSCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O
Show InChI InChI=1S/C48H77N9O16S/c1-22(2)17-31(51-41(65)30(15-16-74-10)50-47(71)39(26(9)58)57-40(64)29(49)19-27-11-13-28(59)14-12-27)44(68)55-38(25(7)8)46(70)56-37(24(5)6)45(69)53-33(21-36(62)63)42(66)52-32(20-35(60)61)43(67)54-34(48(72)73)18-23(3)4/h11-14,22-26,29-34,37-39,58-59H,15-21,49H2,1-10H3,(H,50,71)(H,51,65)(H,52,66)(H,53,69)(H,54,67)(H,55,68)(H,56,70)(H,57,64)(H,60,61)(H,62,63)(H,72,73)/t26-,29+,30+,31+,32+,33+,34+,37+,38+,39+/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 3.60E+4n/an/an/an/an/an/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...)
BDBM50013372
PNG
(CHEMBL2371373 | Tyr-Thr-Met-Leu-Val-Val-Asn-Asp-Le...)
Show SMILES CSCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O
Show InChI InChI=1S/C48H77N9O16S/c1-22(2)17-31(51-41(65)30(15-16-74-10)50-47(71)39(26(9)58)57-40(64)29(49)19-27-11-13-28(59)14-12-27)44(68)55-38(25(7)8)46(70)56-37(24(5)6)45(69)53-33(21-36(62)63)42(66)52-32(20-35(60)61)43(67)54-34(48(72)73)18-23(3)4/h11-14,22-26,29-34,37-39,58-59H,15-21,49H2,1-10H3,(H,50,71)(H,51,65)(H,52,66)(H,53,69)(H,54,67)(H,55,68)(H,56,70)(H,57,64)(H,60,61)(H,62,63)(H,72,73)/t26-,29+,30+,31+,32+,33+,34+,37+,38+,39+/m1/s1
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 1.10E+5n/an/an/an/an/an/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