null

SMILES O=C(Cc1ccc2ccccc2c1)Nc1cc(n[nH]1)C1CC1

InChI Key InChIKey=RIGZCVNCFXYBEG-UHFFFAOYSA-N

PDB links: 1 PDB ID matches this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 7108   

TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
Nerviano Medical Sciences

LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence ATP/[gamma-33P] ATP. After in...More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
Pharmacia Italia

LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 92nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence ATP/[gamma-33P] ATP. After in...More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 5 activator 1 [99-307](Homo sapiens (Human))
Pharmacia Italia

LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence ATP/[gamma-33P] ATP. After in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX998GPubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Pharmacia Italia

LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence ATP/[gamma-33P] ATP. After in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX998GPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Georgetown University

Curated by ChEMBL
LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CDK4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3GBSPubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Georgetown University

Curated by ChEMBL
LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 279nMAssay Description:Inhibition of CDK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3GBSPubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Georgetown University

Curated by ChEMBL
LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
Georgetown University

Curated by ChEMBL
LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 114nMAssay Description:Inhibition of CDK5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3GBSPubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Pharmacia Italia

LigandPNGBDBM7108((N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(2-naphthyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The biochemical activity of compounds was determined by incubation with specific enzymes and substrates in the presence ATP/[gamma-33P] ATP. After in...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX998GPubMed