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Compound Detail

CHEMBL3605637

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CCN(CC)[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 CHEMBL3605637
Phase Preclinical
Structure Type MOL
InChI Key XAEGUOLENLYQPN-RWIUVVJRSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

633.8
MW (Da)
3.12
ALogP
9
HBA
2
HBD
126.9
PSA (Ų)
0.30
QED
1
Ro5 Violations
15
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H47N3O8S
MW 633.81
Aromatic Rings 2
Heavy Atoms 44
NP-Likeness -0.22

Activity Summary

IC50 1 meas. best 8.14
Ki 1 meas. best 10.85

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 10.85 10.85 0.0 1
Human immunodeficiency virus 1
CHEMBL378
IC50 8.14 8.14 7.2 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 0.014 nM 10.85 Inhibition of HIV1 protease 26306007
Human immunodeficiency virus 1 IC50 = 7.2 nM 8.14 Antiviral activity against HIV1 LAI infected in human MT2 cells 26306007

Literature References

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

Data from ChEMBL 36 via Core Engine