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BDBM50103878 Acetic acid 8-allyl-2-oxo-2H-chromen-7-yl ester::CHEMBL77169

SMILES: CC(=O)Oc1ccc2ccc(=O)oc2c1CC=C

InChI Key: InChIKey=SVCVRRCALFDFGG-UHFFFAOYSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50103878   
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
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50103878
PNG
(Acetic acid 8-allyl-2-oxo-2H-chromen-7-yl ester | ...)
Show SMILES CC(=O)Oc1ccc2ccc(=O)oc2c1CC=C
Show InChI InChI=1S/C14H12O4/c1-3-4-11-12(17-9(2)15)7-5-10-6-8-13(16)18-14(10)11/h3,5-8H,1,4H2,2H3
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 820n/an/an/an/an/an/a



Seoul National University

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-alpha-reductase type 1 in cell culture system using LNCaP cells (androgen-sensitive human prostatic cancer cell line)


Bioorg Med Chem Lett 11: 2361-3 (2001)


BindingDB Entry DOI: 10.7270/Q2RR1ZS9
More data for this
Ligand-Target Pair
5α-Reductase 1 (5α-R1)


(Homo sapiens (Human))
BDBM50103878
PNG
(Acetic acid 8-allyl-2-oxo-2H-chromen-7-yl ester | ...)
Show SMILES CC(=O)Oc1ccc2ccc(=O)oc2c1CC=C
Show InChI InChI=1S/C14H12O4/c1-3-4-11-12(17-9(2)15)7-5-10-6-8-13(16)18-14(10)11/h3,5-8H,1,4H2,2H3
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 0.200n/an/an/an/an/an/a



Seoul National University

Curated by ChEMBL


Assay Description
Inhibitory activity against 5-alpha-reductase type 1 in cell culture system using LNCaP cells (androgen-sensitive human prostatic cancer cell line)


Bioorg Med Chem Lett 11: 2361-3 (2001)


BindingDB Entry DOI: 10.7270/Q2RR1ZS9
More data for this
Ligand-Target Pair