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Compound Detail

CHEMBL161542

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Cc1c(Cl)c(=O)oc2c3c(ccc12)OC(C)(C)[C@H](OC(=O)C12CCC(C)(C(=O)O1)C2(C)C)[C@@H]3OC(=O)C12CCC(C)(C(=O)O1)C2(C)C

Basic Information

ChEMBL ID CHEMBL161542
Phase Preclinical
Structure Type MOL
InChI Key PJOCQUFJLKSOCE-QMYDHGACSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

671.1
MW (Da)
5.67
ALogP
11
HBA
0
HBD
144.6
PSA (Ų)
0.23
QED
3
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H39ClO11
MW 671.14
Aromatic Rings 2
Heavy Atoms 47
NP-Likeness 1.32

Activity Summary

EC50 1 meas. best 5.7
IC50 1 meas.

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
H9
CHEMBL614806
EC50 5.7 5.7 2010.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
H9 EC50 = 2010.0 nM 5.7 Inhibitory activity against HIV-1 replication in H9 lymphocytes 11262077

Literature References

PubMed DOI Target Context # Activities
11262077 10.1021/jm000070g H9 2
11262077 10.1021/jm000070g ADMET 1

Data from ChEMBL 36 via Core Engine