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BDBM50041326 4-((2,3-dihydro-1H-inden-2-yl)methyl)pyridine::4-Indan-2-ylmethyl-pyridine::CHEMBL24593

SMILES: C(C1Cc2ccccc2C1)c1ccncc1

InChI Key: InChIKey=CZYPOFQRPJSQFH-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50041326   
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 19A1


(Homo sapiens (Human))
BDBM50041326
PNG
(4-((2,3-dihydro-1H-inden-2-yl)methyl)pyridine | 4-...)
Show SMILES C(C1Cc2ccccc2C1)c1ccncc1
Show InChI InChI=1S/C15H15N/c1-2-4-15-11-13(10-14(15)3-1)9-12-5-7-16-8-6-12/h1-8,13H,9-11H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2.40E+3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of aromatase


J Med Chem 51: 2481-91 (2008)


Article DOI: 10.1021/jm701314u
BindingDB Entry DOI: 10.7270/Q2GX4CF5
More data for this
Ligand-Target Pair
Cytochrome P450 19A1


(Homo sapiens (Human))
BDBM50041326
PNG
(4-((2,3-dihydro-1H-inden-2-yl)methyl)pyridine | 4-...)
Show SMILES C(C1Cc2ccccc2C1)c1ccncc1
Show InChI InChI=1S/C15H15N/c1-2-4-15-11-13(10-14(15)3-1)9-12-5-7-16-8-6-12/h1-8,13H,9-11H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 2.40E+3n/an/an/an/an/an/a



Universität des Saarlandes

Curated by ChEMBL


Assay Description
Inhibition of human Placental Cytochrome P450 19A1 in vitro using human placental microsomes and testosterone


J Med Chem 37: 1275-81 (1994)


BindingDB Entry DOI: 10.7270/Q2XD10QX
More data for this
Ligand-Target Pair