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BDBM50007093 CHEMBL3237564

SMILES: N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O

InChI Key: InChIKey=WPELTQURDISYSR-GXTWGEPZSA-N

Data: 6 IC50

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 6 hits for monomerid = 50007093   
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
Tyrosine-protein kinase SYK


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a 10n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of human SYK (360 to 635) using biotin-EPEGDYEEVLE as substrate preincubated for 10 mins followed by substrate/ATP/[33Pgamma]ATP addition ...


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase SYK


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a 251n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of SYK in human whole blood assessed as anti-human IgM-induced CD69 protein expression preincubated for 30 mins followed by anti-human IgM...


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a>5.00E+4n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 in human liver microsomal fraction assessed as dextromethorphan O-demethylase preincubated for 10 mins followed by NADPH additio...


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a>5.00E+4n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomal fraction assessed as midazolam-1'-hydroxylation preincubated for 10 mins followed by NADPH addition me...


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a>5.00E+4n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 in human liver microsomal fraction assessed as diclofenac-4'-hydroxylation preincubated for 10 mins followed by NADPH addition m...


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50007093
PNG
(CHEMBL3237564)
Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r|
Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1
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n/an/a 7.94E+3n/an/an/an/an/an/a



Hoffmann-La Roche Inc.

Curated by ChEMBL


Assay Description
Inhibition of human ERG expressed in CHO cells by patch clamp method


J Med Chem 57: 2683-91 (2014)


Article DOI: 10.1021/jm401982j
BindingDB Entry DOI: 10.7270/Q2HT2QTR
More data for this
Ligand-Target Pair