BindingDB logo
myBDB logout

BDBM4086 2,3,7,8-tetrahydroxy-5-[(4-nitrophenyl)methyl]-5,6-dihydrophenanthridin-6-one::Phenanthridinone deriv. 5h

SMILES: Oc1ccc2c3cc(O)c(O)cc3n(Cc3ccc(cc3)[N+]([O-])=O)c(=O)c2c1O

InChI Key: InChIKey=KJDQVGMYCXBXIU-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 4086   
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
cAMP-Dependent Protein Kinase (PKA)


(Bos taurus (bovine))
BDBM4086
PNG
(2,3,7,8-tetrahydroxy-5-[(4-nitrophenyl)methyl]-5,6...)
Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(Cc3ccc(cc3)[N+]([O-])=O)c(=O)c2c1O
Show InChI InChI=1S/C20H14N2O7/c23-15-6-5-12-13-7-16(24)17(25)8-14(13)21(20(27)18(12)19(15)26)9-10-1-3-11(4-2-10)22(28)29/h1-8,23-26H,9H2
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 3.09E+5n/an/an/an/a7.430



Pfizer



Assay Description
IC50 is the inhibitor concentration, which inhibits 50% of PKA activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] label...


J Med Chem 37: 2224-31 (1994)


Article DOI: 10.1021/jm00040a015
BindingDB Entry DOI: 10.7270/Q27M0648
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM4086
PNG
(2,3,7,8-tetrahydroxy-5-[(4-nitrophenyl)methyl]-5,6...)
Show SMILES Oc1ccc2c3cc(O)c(O)cc3n(Cc3ccc(cc3)[N+]([O-])=O)c(=O)c2c1O
Show InChI InChI=1S/C20H14N2O7/c23-15-6-5-12-13-7-16(24)17(25)8-14(13)21(20(27)18(12)19(15)26)9-10-1-3-11(4-2-10)22(28)29/h1-8,23-26H,9H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
PubMed
n/an/a 6.10E+4n/an/an/an/a7.430



Pfizer



Assay Description
IC50 is the inhibitor concentration, which inhibits 50% of pp60c-src activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] ...


J Med Chem 37: 2224-31 (1994)


Article DOI: 10.1021/jm00040a015
BindingDB Entry DOI: 10.7270/Q27M0648
More data for this
Ligand-Target Pair