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
Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cytochrome P450 19A1 (Homo sapiens (Human)) | BDBM50041326![]() (4-((2,3-dihydro-1H-inden-2-yl)methyl)pyridine | 4-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/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![]() (4-((2,3-dihydro-1H-inden-2-yl)methyl)pyridine | 4-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/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 |