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BDBM50052059 5-Methyl-5-phenyl-6-thia-10b-aza-benzo[e]azulen-4-one::CHEMBL316094

SMILES: CC1(Sc2ccccc2-n2cccc2C1=O)c1ccccc1

InChI Key: InChIKey=SSDOAOBSEPIANH-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50052059   
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
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50052059
PNG
(5-Methyl-5-phenyl-6-thia-10b-aza-benzo[e]azulen-4-...)
Show SMILES CC1(Sc2ccccc2-n2cccc2C1=O)c1ccccc1
Show InChI InChI=1S/C19H15NOS/c1-19(14-8-3-2-4-9-14)18(21)16-11-7-13-20(16)15-10-5-6-12-17(15)22-19/h2-13H,1H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 350n/an/an/an/an/an/a



Institute of Experimental Botany ASCR & Palack£ University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 reverse transcriptase


Bioorg Med Chem 23: 5247-63 (2015)


Article DOI: 10.1016/j.bmc.2015.06.016
BindingDB Entry DOI: 10.7270/Q20P131K
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50052059
PNG
(5-Methyl-5-phenyl-6-thia-10b-aza-benzo[e]azulen-4-...)
Show SMILES CC1(Sc2ccccc2-n2cccc2C1=O)c1ccccc1
Show InChI InChI=1S/C19H15NOS/c1-19(14-8-3-2-4-9-14)18(21)16-11-7-13-20(16)15-10-5-6-12-17(15)22-19/h2-13H,1H3
PDB
MMDB

UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/a 5.00E+3n/an/an/an/an/an/a



Universitá di Siena

Curated by ChEMBL


Assay Description
Compound was tested for Inhibition of HIV-1 RT activity.


J Med Chem 39: 2672-80 (1996)


Article DOI: 10.1021/jm950702c
BindingDB Entry DOI: 10.7270/Q21R6PM4
More data for this
Ligand-Target Pair