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Compound Detail

CHEMBL274008

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Cc1cn(C2C=CC(COP(=O)(OCC(F)(F)F)OCC(F)(F)F)O2)c(=O)[nH]c1=O

Basic Information

ChEMBL ID CHEMBL274008
Phase Preclinical
Structure Type MOL
InChI Key ATTNZXDAJMWKIX-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

468.2
MW (Da)
2.58
ALogP
8
HBA
1
HBD
108.8
PSA (Ų)
0.36
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H15F6N2O7P
MW 468.24
Aromatic Rings 1
Heavy Atoms 30
NP-Likeness 0.15

Activity Summary

EC50 1 meas. best 4.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
C8166
CHEMBL614533
EC50 4.82 4.82 15000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
C8166 EC50 = 15000.0 nM 4.82 Ability to inhibit the replication of HIV-1 IIIB infected C8166 cells -

Literature References

PubMed DOI Target Context # Activities
- 10.1016/S0960-894X(00)80315-7 C8166 2
- 10.1016/S0960-894X(00)80315-7 Unchecked 1

Data from ChEMBL 36 via Core Engine