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Compound Detail

CHEMBL4859319

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COC(=O)[C@H](Cc1ccc(O[P@@](=O)(CO[C@H](C)Cn2cnc3c(N)ncnc32)N[C@@H](C)C(=O)OC(C)C)cc1)NC(=O)C(F)(F)F

Basic Information

ChEMBL ID CHEMBL4859319
Phase Preclinical
Structure Type MOL
InChI Key AWAXEHIBYSVGLN-BHAMOJACSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

673.6
MW (Da)
2.74
ALogP
13
HBA
3
HBD
198.9
PSA (Ų)
0.16
QED
2
Ro5 Violations
15
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H35F3N7O8P
MW 673.59
Aromatic Rings 3
Heavy Atoms 46
NP-Likeness -0.39

Activity Summary

EC50 2 meas. best 9.57

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatitis B virus
CHEMBL613497
EC50 9.57 9.57 0.3 1
Human immunodeficiency virus 1
CHEMBL378
EC50 6.82 6.82 150.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34713696 10.1021/acs.jmedchem.1c01444 Human immunodeficiency virus 1 1
34713696 10.1021/acs.jmedchem.1c01444 MT4 1
34713696 10.1021/acs.jmedchem.1c01444 Hepatitis B virus 1
34713696 10.1021/acs.jmedchem.1c01444 HepG2 1

Data from ChEMBL 36 via Core Engine