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BDBM50105809 4-Amino-N-isopropyl-N-(2-phenyl-2H-pyrazol-3-yl)-benzenesulfonamide::CHEMBL121323

SMILES: CC(C)N(c1ccnn1-c1ccccc1)S(=O)(=O)c1ccc(N)cc1

InChI Key: InChIKey=XBGCSAANSNGXGH-UHFFFAOYSA-N

Data: 4 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50105809   
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
Cytochrome P450 2C8


(Homo sapiens (Human))
BDBM50105809
PNG
(4-Amino-N-isopropyl-N-(2-phenyl-2H-pyrazol-3-yl)-b...)
Show SMILES CC(C)N(c1ccnn1-c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C18H20N4O2S/c1-14(2)22(25(23,24)17-10-8-15(19)9-11-17)18-12-13-20-21(18)16-6-4-3-5-7-16/h3-14H,19H2,1-2H3
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 3.00E+4n/an/an/an/an/an/a



Université Paris V

Curated by ChEMBL


Assay Description
Inhibitory effect on human recombinant liver Cytochrome P450 2C8 expressed in yeast strain


J Med Chem 44: 3622-31 (2001)


BindingDB Entry DOI: 10.7270/Q20Z72KC
More data for this
Ligand-Target Pair
Cytochrome P450 2C18


(Homo sapiens (Human))
BDBM50105809
PNG
(4-Amino-N-isopropyl-N-(2-phenyl-2H-pyrazol-3-yl)-b...)
Show SMILES CC(C)N(c1ccnn1-c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C18H20N4O2S/c1-14(2)22(25(23,24)17-10-8-15(19)9-11-17)18-12-13-20-21(18)16-6-4-3-5-7-16/h3-14H,19H2,1-2H3
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 3.00E+3n/an/an/an/an/an/a



Université Paris V

Curated by ChEMBL


Assay Description
Inhibitory effect on human recombinant liver cytochrome P450 2C18 expressed in yeast strain


J Med Chem 44: 3622-31 (2001)


BindingDB Entry DOI: 10.7270/Q20Z72KC
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50105809
PNG
(4-Amino-N-isopropyl-N-(2-phenyl-2H-pyrazol-3-yl)-b...)
Show SMILES CC(C)N(c1ccnn1-c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C18H20N4O2S/c1-14(2)22(25(23,24)17-10-8-15(19)9-11-17)18-12-13-20-21(18)16-6-4-3-5-7-16/h3-14H,19H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 1.30E+5n/an/an/an/an/an/a



Université Paris V

Curated by ChEMBL


Assay Description
Inhibitory effect on human recombinant liver cytochrome P450 2C19 expressed in yeast strain


J Med Chem 44: 3622-31 (2001)


BindingDB Entry DOI: 10.7270/Q20Z72KC
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50105809
PNG
(4-Amino-N-isopropyl-N-(2-phenyl-2H-pyrazol-3-yl)-b...)
Show SMILES CC(C)N(c1ccnn1-c1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C18H20N4O2S/c1-14(2)22(25(23,24)17-10-8-15(19)9-11-17)18-12-13-20-21(18)16-6-4-3-5-7-16/h3-14H,19H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 8.00E+4n/an/an/an/an/an/a



Université Paris V

Curated by ChEMBL


Assay Description
Inhibitory effect on human recombinant liver cytochrome P450 2C9 expressed in yeast strain


J Med Chem 44: 3622-31 (2001)


BindingDB Entry DOI: 10.7270/Q20Z72KC
More data for this
Ligand-Target Pair