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BDBM8906 6-(pyridin-3-yl)naphthalen-2-ol::6-Pyridin-3-ylnaphthalen-2-ol::Pyridine-substituted naphthalene 3::US9271963, 3

SMILES: Oc1ccc2cc(ccc2c1)-c1cccnc1

InChI Key: InChIKey=MDXMZUQFVFTPDO-UHFFFAOYSA-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 = 8906   
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 11B1, mitochondrial


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
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Article
PubMed
n/an/a 2.67E+3n/an/an/an/a7.437



Saarland University



Assay Description
The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...


J Med Chem 48: 6632-42 (2005)


Article DOI: 10.1021/jm0503704
BindingDB Entry DOI: 10.7270/Q2H41PNT
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
PDB

UniProtKB/SwissProt

antibodypedia
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Article
PubMed
n/an/a 23n/an/an/an/an/an/a



Saarland University



Assay Description
The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...


J Med Chem 48: 6632-42 (2005)


Article DOI: 10.1021/jm0503704
BindingDB Entry DOI: 10.7270/Q2H41PNT
More data for this
Ligand-Target Pair
Cytochrome P450 19A1


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
PDB
MMDB

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Article
PubMed
n/an/a 2.70E+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 11B1, mitochondrial


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
PDB

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US Patent
n/an/a 715n/an/an/an/an/a37



UNIVERSITAT DES SAARLANDES

US Patent


Assay Description
V79 MZh11B1 and V79 MZh 11B2 cells (8˙10^5 cells per well) were grown to confluency on 24-well cell culture plates with 1.9 cm^2 culture area per...


US Patent US9271963 (2016)


BindingDB Entry DOI: 10.7270/Q2445KBN
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
PDB

UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem

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US Patent
n/an/a 23n/an/an/an/an/a37



UNIVERSITAT DES SAARLANDES

US Patent


Assay Description
V79 MZh11B1 and V79 MZh 11B2 cells (8˙10^5 cells per well) were grown to confluency on 24-well cell culture plates with 1.9 cm^2 culture area per...


US Patent US9271963 (2016)


BindingDB Entry DOI: 10.7270/Q2445KBN
More data for this
Ligand-Target Pair
Cytochrome P450 19A1


(Homo sapiens (Human))
BDBM8906
PNG
(6-(pyridin-3-yl)naphthalen-2-ol | 6-Pyridin-3-ylna...)
Show SMILES Oc1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11NO/c17-15-6-5-11-8-12(3-4-13(11)9-15)14-2-1-7-16-10-14/h1-10,17H
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
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Purchase

PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a>3.60E+4n/an/an/an/an/an/a



Saarland University



Assay Description
The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta-3H] Androstenedione during aromatization. After incubation, the re...


J Med Chem 48: 6632-42 (2005)


Article DOI: 10.1021/jm0503704
BindingDB Entry DOI: 10.7270/Q2H41PNT
More data for this
Ligand-Target Pair