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Compound Detail

CHEMBL3605641

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COC(=O)N[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 CHEMBL3605641
Phase Preclinical
Structure Type MOL
InChI Key PSQWVVVMNRVUFI-HJCZHRQASA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

635.7
MW (Da)
2.14
ALogP
10
HBA
3
HBD
162.0
PSA (Ų)
0.30
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 C30H41N3O10S
MW 635.74
Aromatic Rings 2
Heavy Atoms 44
NP-Likeness -0.17

Activity Summary

IC50 1 meas. best 8.43
Ki 1 meas. best 10.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 10.62 10.62 0.0 1
Human immunodeficiency virus 1
CHEMBL378
IC50 8.43 8.43 3.7 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 0.024 nM 10.62 Inhibition of HIV1 protease 26306007
Human immunodeficiency virus 1 IC50 = 3.7 nM 8.43 Antiviral activity against HIV1 LAI infected in human MT2 cells 26306007

Literature References

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

Data from ChEMBL 36 via Core Engine