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SMILES: CC1(C)CC(=O)c2c(C1)nc1n(Cc3ccccc3)cc(C#N)c1c2-c1c(F)cccc1F

InChI Key: InChIKey=ZKOSGFGLYIQUED-UHFFFAOYSA-N

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 4 hits for monomerid = 50532854   
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)
BDBM50532854
PNG
(CHEMBL4588569)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1n(Cc3ccccc3)cc(C#N)c1c2-c1c(F)cccc1F |(64.49,-40.46,;65.82,-39.68,;64.89,-38.49,;66.31,-41.17,;67.81,-41.5,;68.03,-43.03,;68.84,-40.35,;68.36,-38.89,;66.86,-38.57,;69.39,-37.75,;70.89,-38.06,;72.13,-37.16,;72.13,-35.62,;70.8,-34.84,;70.8,-33.3,;69.46,-32.54,;68.13,-33.31,;68.13,-34.86,;69.47,-35.62,;73.38,-38.06,;72.9,-39.53,;73.81,-40.78,;74.71,-42.03,;71.36,-39.53,;70.34,-40.66,;71.1,-43.01,;72.61,-43.32,;73.64,-42.17,;73.09,-44.79,;72.06,-45.94,;70.55,-45.62,;70.08,-44.12,;68.57,-43.77,)|
Show InChI InChI=1S/C27H21F2N3O/c1-27(2)11-20-24(21(33)12-27)25(23-18(28)9-6-10-19(23)29)22-17(13-30)15-32(26(22)31-20)14-16-7-4-3-5-8-16/h3-10,15H,11-12,14H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 360n/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 RT using 17-mer DNA/Alexa Fluor 488 5'-end labeled DNA/Alexa Fluor 555-aha-dUTP as primer/template/substrate preincubated for 10 m...


Bioorg Med Chem Lett 26: 4101-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.065
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50532854
PNG
(CHEMBL4588569)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1n(Cc3ccccc3)cc(C#N)c1c2-c1c(F)cccc1F |(64.49,-40.46,;65.82,-39.68,;64.89,-38.49,;66.31,-41.17,;67.81,-41.5,;68.03,-43.03,;68.84,-40.35,;68.36,-38.89,;66.86,-38.57,;69.39,-37.75,;70.89,-38.06,;72.13,-37.16,;72.13,-35.62,;70.8,-34.84,;70.8,-33.3,;69.46,-32.54,;68.13,-33.31,;68.13,-34.86,;69.47,-35.62,;73.38,-38.06,;72.9,-39.53,;73.81,-40.78,;74.71,-42.03,;71.36,-39.53,;70.34,-40.66,;71.1,-43.01,;72.61,-43.32,;73.64,-42.17,;73.09,-44.79,;72.06,-45.94,;70.55,-45.62,;70.08,-44.12,;68.57,-43.77,)|
Show InChI InChI=1S/C27H21F2N3O/c1-27(2)11-20-24(21(33)12-27)25(23-18(28)9-6-10-19(23)29)22-17(13-30)15-32(26(22)31-20)14-16-7-4-3-5-8-16/h3-10,15H,11-12,14H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.69E+3n/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 RT Y181C mutant using 17-mer DNA/Alexa Fluor 488 5'-end labeled DNA/Alexa Fluor 555-aha-dUTP as primer/template/substrate preincub...


Bioorg Med Chem Lett 26: 4101-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.065
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50532854
PNG
(CHEMBL4588569)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1n(Cc3ccccc3)cc(C#N)c1c2-c1c(F)cccc1F |(64.49,-40.46,;65.82,-39.68,;64.89,-38.49,;66.31,-41.17,;67.81,-41.5,;68.03,-43.03,;68.84,-40.35,;68.36,-38.89,;66.86,-38.57,;69.39,-37.75,;70.89,-38.06,;72.13,-37.16,;72.13,-35.62,;70.8,-34.84,;70.8,-33.3,;69.46,-32.54,;68.13,-33.31,;68.13,-34.86,;69.47,-35.62,;73.38,-38.06,;72.9,-39.53,;73.81,-40.78,;74.71,-42.03,;71.36,-39.53,;70.34,-40.66,;71.1,-43.01,;72.61,-43.32,;73.64,-42.17,;73.09,-44.79,;72.06,-45.94,;70.55,-45.62,;70.08,-44.12,;68.57,-43.77,)|
Show InChI InChI=1S/C27H21F2N3O/c1-27(2)11-20-24(21(33)12-27)25(23-18(28)9-6-10-19(23)29)22-17(13-30)15-32(26(22)31-20)14-16-7-4-3-5-8-16/h3-10,15H,11-12,14H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 360n/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 RT using 17-mer DNA/Alexa Fluor 488 5'-end labeled DNA/Alexa Fluor 555-aha-dUTP as primer/template/substrate preincubated for 10 m...


Bioorg Med Chem Lett 26: 4101-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.065
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50532854
PNG
(CHEMBL4588569)
Show SMILES CC1(C)CC(=O)c2c(C1)nc1n(Cc3ccccc3)cc(C#N)c1c2-c1c(F)cccc1F |(64.49,-40.46,;65.82,-39.68,;64.89,-38.49,;66.31,-41.17,;67.81,-41.5,;68.03,-43.03,;68.84,-40.35,;68.36,-38.89,;66.86,-38.57,;69.39,-37.75,;70.89,-38.06,;72.13,-37.16,;72.13,-35.62,;70.8,-34.84,;70.8,-33.3,;69.46,-32.54,;68.13,-33.31,;68.13,-34.86,;69.47,-35.62,;73.38,-38.06,;72.9,-39.53,;73.81,-40.78,;74.71,-42.03,;71.36,-39.53,;70.34,-40.66,;71.1,-43.01,;72.61,-43.32,;73.64,-42.17,;73.09,-44.79,;72.06,-45.94,;70.55,-45.62,;70.08,-44.12,;68.57,-43.77,)|
Show InChI InChI=1S/C27H21F2N3O/c1-27(2)11-20-24(21(33)12-27)25(23-18(28)9-6-10-19(23)29)22-17(13-30)15-32(26(22)31-20)14-16-7-4-3-5-8-16/h3-10,15H,11-12,14H2,1-2H3
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.69E+3n/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Inhibition of HIV1 RT Y181C mutant using 17-mer DNA/Alexa Fluor 488 5'-end labeled DNA/Alexa Fluor 555-aha-dUTP as primer/template/substrate preincub...


Bioorg Med Chem Lett 26: 4101-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.06.065
More data for this
Ligand-Target Pair