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Compound Detail

CHEMBL3115365

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N#Cc1cc(Cl)cc(Oc2c(C(F)(F)F)ccn(Cc3n[nH]c4cnccc34)c2=O)c1

Basic Information

ChEMBL ID CHEMBL3115365
Phase Preclinical
Structure Type MOL
InChI Key LFPVKYVDUAEZML-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

445.8
MW (Da)
4.50
ALogP
6
HBA
1
HBD
96.6
PSA (Ų)
0.50
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H11ClF3N5O2
MW 445.79
Aromatic Rings 4
Heavy Atoms 31
NP-Likeness -1.43

Activity Summary

IC50 1 meas. best 8.22

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 8.22 8.22 6.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 40.0 mL.min-1.kg-1 Rattus norvegicus
F 74.0 % Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 6.0 nM 8.22 Inhibition of HIV wild-type reverse transcriptase by electrochemiluminescence as... 24412110

Literature References

PubMed DOI Target Context # Activities
24412110 10.1016/j.bmcl.2013.12.070 Rattus norvegicus 2
24412110 10.1016/j.bmcl.2013.12.070 Human immunodeficiency virus 2
24412110 10.1016/j.bmcl.2013.12.070 No relevant target 1
24412110 10.1016/j.bmcl.2013.12.070 Unchecked 1

Data from ChEMBL 36 via Core Engine