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BDBM50285359 5-Ethyl-11-methyl-5,11-dihydro-1,5,6,11-tetraaza-dibenzo[a,d]cyclohepten-10-one::CHEMBL298243

SMILES: CCN1c2cccnc2N(C)C(=O)c2cccnc12

InChI Key: InChIKey=RUXYPOYUXWFXNP-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50285359   
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
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50285359
PNG
(5-Ethyl-11-methyl-5,11-dihydro-1,5,6,11-tetraaza-d...)
Show SMILES CCN1c2cccnc2N(C)C(=O)c2cccnc12
Show InChI InChI=1S/C14H14N4O/c1-3-18-11-7-5-9-16-13(11)17(2)14(19)10-6-4-8-15-12(10)18/h4-9H,3H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 1.30E+3n/an/an/an/an/an/a



Boehringer Ingelheim Pharmaceuticals

Curated by ChEMBL


Assay Description
In vitro for inhibition of HIV-1 reverse transcriptase.


J Med Chem 38: 1406-10 (1995)


BindingDB Entry DOI: 10.7270/Q2MG7NJQ
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50285359
PNG
(5-Ethyl-11-methyl-5,11-dihydro-1,5,6,11-tetraaza-d...)
Show SMILES CCN1c2cccnc2N(C)C(=O)c2cccnc12
Show InChI InChI=1S/C14H14N4O/c1-3-18-11-7-5-9-16-13(11)17(2)14(19)10-6-4-8-15-12(10)18/h4-9H,3H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
n/an/a 1.30E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against HIV-1 Reverse transcriptase(RT) was determined


Bioorg Med Chem Lett 5: 163-166 (1995)


Article DOI: 10.1016/0960-894X(94)00478-X
BindingDB Entry DOI: 10.7270/Q22R3RM4
More data for this
Ligand-Target Pair