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Compound Detail

CHEMBL5438239

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O=C(CN1CCN(S(=O)(=O)c2ccc([N+](=O)[O-])cc2)CC1)N[C@@H](Cc1cc(F)cc(F)c1)c1nc2ccccc2c(=O)n1-c1ccc(S(=O)(=O)N2CCS(=O)(=O)CC2)cc1

Basic Information

ChEMBL ID CHEMBL5438239
Phase Preclinical
Structure Type MOL
InChI Key LMNOOFUZLFUHQC-DHUJRADRSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

886.0
MW (Da)
2.40
ALogP
13
HBA
1
HBD
219.3
PSA (Ų)
0.14
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H37F2N7O10S3
MW 885.95
Aromatic Rings 5
Heavy Atoms 60
NP-Likeness -1.57

Activity Summary

EC50 2 meas. best 5.71

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 2
CHEMBL380
EC50 5.71 5.71 1970.0 1
Human immunodeficiency virus 1
CHEMBL378
EC50 5.52 5.52 3040.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
38054267 10.1021/acs.jmedchem.3c01647 ADMET 3
38054267 10.1021/acs.jmedchem.3c01647 MT4 1
38054267 10.1021/acs.jmedchem.3c01647 Human immunodeficiency virus 1 1
38054267 10.1021/acs.jmedchem.3c01647 Human immunodeficiency virus 2 1

Data from ChEMBL 36 via Core Engine