BDBM50246956 1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thiazol-3-yl)methyl)isothiourea::CHEMBL452864

SMILES C(S\C(NC1CCCCC1)=N/C1CCCCC1)C1=CSC2=NCCN12

InChI Key InChIKey=ZEZPDHKACVMMCD-UHFFFAOYSA-N

Data  13 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 13 hits for monomerid = 50246956   

TargetC-X-C chemokine receptor type 4(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 11nMAssay Description:Activity at CXCR4 in human CEM cells assessed as inhibition of CXCL12-induced calcium mobilizationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetC-X-C chemokine receptor type 4(Rat)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 29nMAssay Description:Activity at CXCR4 in rat IR983F cells assessed as inhibition of CXCL12-induced cell migrationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetC-X-C chemokine receptor type 4(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 48nMAssay Description:Displacement of [125I]CXCL12 from CXCR4 in human CEM cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetC-X-C chemokine receptor type 4(Rat)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 55nMAssay Description:Displacement of [125I]CXCL12 from CXCR4 in rat IR983F cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetC-X-C chemokine receptor type 4(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 58nMAssay Description:Activity at CXCR4 in human Jurkat T cells assessed as inhibition of CXCL12-induced cell migrationMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetC-C chemokine receptor type 7(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of CCR7More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 3.86E+3nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 2D6(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 6.78E+3nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 8.50E+3nMAssay Description:Displacement of [3H]dofetilide from human recombinant ERG expressed in HEK293 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C9More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 1A2(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 2C19(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50246956(1,3-dicyclohexyl-2-((5,6-dihydroimidazo[2,1-b]thia...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of human recombinant ERG in CHOK1 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed