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Compound Detail

CHEMBL3605643

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CN[C@H]1CO[C@@H]2OC[C@H](OC(=O)N[C@@H](Cc3ccccc3)[C@H](O)CN(CC(C)C)S(=O)(=O)c3ccc(OC)cc3)[C@@H]21

Basic Information

ChEMBL ID CHEMBL3605643
Phase Preclinical
Structure Type MOL
InChI Key RTQZESJLDDKIAO-HJCZHRQASA-N
1
Targets
4
Activities
3
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

591.7
MW (Da)
2.00
ALogP
9
HBA
3
HBD
135.7
PSA (Ų)
0.32
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H41N3O8S
MW 591.73
Aromatic Rings 2
Heavy Atoms 41
NP-Likeness -0.04

Activity Summary

EC50 2 meas. best 7.54
IC50 1 meas. best 7.46
Ki 1 meas.

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 7.54 7.52 29.0 2
Human immunodeficiency virus 1
CHEMBL378
IC50 7.46 7.46 35.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
26306007 10.1021/acs.jmedchem.5b00900 Human immunodeficiency virus 1 8
26306007 10.1021/acs.jmedchem.5b00900 Protease 1

Data from ChEMBL 36 via Core Engine