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Compound Detail

CHEMBL1791154

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O=c1[nH]c(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1-c1ccno1

Basic Information

ChEMBL ID CHEMBL1791154
Phase Preclinical
Structure Type MOL
InChI Key KPQSIUAPOSYYJU-FXBDTBDDSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

295.2
MW (Da)
-1.17
ALogP
8
HBA
3
HBD
130.6
PSA (Ų)
0.65
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C12H13N3O6
MW 295.25
Aromatic Rings 2
Heavy Atoms 21
NP-Likeness 0.25

Activity Summary

IC50 1 meas. best 4.44

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Thymidine kinase
CHEMBL1820
IC50 4.44 4.44 36000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Thymidine kinase IC50 = 36000.0 nM 4.44 Binding affinity towards HSV-1 thymidine kinase 8941385

Literature References

PubMed DOI Target Context # Activities
8388474 10.1021/jm00057a003 Human alphaherpesvirus 1 5
8388474 10.1021/jm00057a003 Human alphaherpesvirus 2 3
8388474 10.1021/jm00057a003 Human alphaherpesvirus 3 2
8388474 10.1021/jm00057a003 Vesicular stomatitis virus 2
8388474 10.1021/jm00057a003 Cell line 2
8941385 10.1021/jm960278v Thymidine kinase 1
8388474 10.1021/jm00057a003 Vaccinia virus 1

Data from ChEMBL 36 via Core Engine