null

SMILES O=C(Nc1sc2CCCCc2c1C#N)c1ccccc1

InChI Key InChIKey=OKFHWMLGUMHKFC-UHFFFAOYSA-N

  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 7 hits for monomerid = 50241256   

TargetRAC-gamma serine/threonine-protein kinase(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataKd: >4.00E+4nMAssay Description:Binding affinity to human AKT3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WS8T4CPubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of JNK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WS8T4CPubMed
TargetRAC-gamma serine/threonine-protein kinase(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataKd: >1.00E+4nMAssay Description:Binding affinity to human AKT3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WS8T4CPubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
GlaxoSmithKline R&D

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant full length JNK1alpha1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB1840PubMed
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
GlaxoSmithKline

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 1.58E+3nMAssay Description:Inhibition of human truncated JNK3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB1840PubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
GlaxoSmithKline R&D

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 1.58E+4nMAssay Description:Inhibition of mitogen-activated protein kinase p38alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TB1840PubMed
TargetVasoactive intestinal polypeptide receptor 1(Rattus norvegicus)
Bristol-Myers Squibb Co.

Curated by ChEMBL
LigandPNGBDBM50241256(CHEMBL233000 | N-(3-cyano-4,5,6,7-tetrahydrobenzo[...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q240QRPubMed