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SMILES: Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N

InChI Key:

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 9 hits for monomerid = 509930   
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
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.20E+4n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods to assess compound activity and IC50. As an exemplary for assessment of the SARS-COV2 Mpro, the C-His6-...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2GB276R
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(2019-nCoV)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.20E+4n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods to assess compound activity and IC50. As an exemplary for assessment of the SARS-COV2 Mpro, the C-His6-...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2GB276R
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<2.20E+4n/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods against multiple coronaviral strains, including HCoV 229E and OC43 strains. The antiviral activity of c...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2GB276R
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<2.00E+3n/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods against multiple coronaviral strains, including HCoV 229E and OC43 strains. The antiviral activity of c...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2B56P00
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<2.00E+3n/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods against multiple coronaviral strains, including HCoV 229E and OC43 strains. The antiviral activity of c...


Citation and Details

BindingDB Entry DOI: 10.7270/Q23B63CF
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(2019-nCoV)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.00E+3n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods to assess compound activity and IC50. As an exemplary for assessment of the SARS-COV2 Mpro, the C-His6-...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2B56P00
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.00E+3n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods against multiple coronaviral strains, including HCoV 229E and OC43 strains. The antiviral activity of c...


Citation and Details

BindingDB Entry DOI: 10.7270/Q23B63CF
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(2019-nCoV)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.00E+3n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods to assess compound activity and IC50. As an exemplary for assessment of the SARS-COV2 Mpro, the C-His6-...


Citation and Details

BindingDB Entry DOI: 10.7270/Q23B63CF
More data for this
Ligand-Target Pair
Replicase polyprotein 1ab


(HCoV-229E)
BDBM509930
PNG
(US11124497, Compound 519 | US11312704, Compound 51...)
Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)N[C@@H](CC1CC1)C(=O)N[C@@H](C[C@@H]1CCNC1=O)C#N |r|
PDB
MMDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a<2.00E+3n/an/an/an/an/an/a


TBA

Assay Description
Compounds were assayed using standard methods against multiple coronaviral strains, including HCoV 229E and OC43 strains. The antiviral activity of c...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2B56P00
More data for this
Ligand-Target Pair