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Compound Detail

CHEMBL4873511

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CC(C)OC(=O)[C@H](C)N[P@](=O)(CO[C@H](C)Cn1cnc2c(N)ncnc21)Oc1ccc(C[C@H](NC(=O)CCc2ccccc2)C(=O)OC2CCCC2)cc1

Basic Information

ChEMBL ID CHEMBL4873511
Phase Preclinical
Structure Type MOL
InChI Key GMUDIWOGCRNFAE-GZGIXZNCSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

763.8
MW (Da)
5.12
ALogP
13
HBA
3
HBD
198.9
PSA (Ų)
0.08
QED
3
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H50N7O8P
MW 763.83
Aromatic Rings 4
Heavy Atoms 54
NP-Likeness -0.22

Activity Summary

EC50 2 meas. best 11.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 11.0 11.0 0.0 1
Hepatitis B virus
CHEMBL613497
EC50 8.36 8.36 4.4 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34713696 10.1021/acs.jmedchem.1c01444 ADMET 5
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 Lysosomal protective protein 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