BindingDB logo
myBDB logout

BDBM3991 1 H-indole-3-alkanamide deriv. 10b::2-(2-{[3-(cyanomethyl)-1H-indol-2-yl]disulfanyl}-1H-indol-3-yl)acetonitrile

SMILES: N#CCc1c(SSc2[nH]c3ccccc3c2CC#N)[nH]c2ccccc12

InChI Key: InChIKey=WRQVNXDOWPRYHH-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 = 3991   
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
Tyrosine-protein kinase transforming protein Src


(Avian sarcoma virus)
BDBM3991
PNG
(1 H-indole-3-alkanamide deriv. 10b | 2-(2-{[3-(cya...)
Show SMILES N#CCc1c(SSc2[nH]c3ccccc3c2CC#N)[nH]c2ccccc12
Show InChI InChI=1S/C20H14N4S2/c21-11-9-15-13-5-1-3-7-17(13)23-19(15)25-26-20-16(10-12-22)14-6-2-4-8-18(14)24-20/h1-8,23-24H,9-10H2
PDB
MMDB

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 2.50E+3n/an/an/an/an/an/a



University of Auckland



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


J Med Chem 37: 598-609 (1994)


Article DOI: 10.1021/jm00031a009
BindingDB Entry DOI: 10.7270/Q2MS3QZH
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM3991
PNG
(1 H-indole-3-alkanamide deriv. 10b | 2-(2-{[3-(cya...)
Show SMILES N#CCc1c(SSc2[nH]c3ccccc3c2CC#N)[nH]c2ccccc12
Show InChI InChI=1S/C20H14N4S2/c21-11-9-15-13-5-1-3-7-17(13)23-19(15)25-26-20-16(10-12-22)14-6-2-4-8-18(14)24-20/h1-8,23-24H,9-10H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 3.20E+4n/an/an/an/a7.422



University of Auckland



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


J Med Chem 37: 598-609 (1994)


Article DOI: 10.1021/jm00031a009
BindingDB Entry DOI: 10.7270/Q2MS3QZH
More data for this
Ligand-Target Pair