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Compound Detail

CHEMBL583567

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COCCNC(=O)[C@@H](NC(=O)[C@](O)(CCN(Cc1ccc(Br)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)Cc1ccccc1)C(C)C

Basic Information

ChEMBL ID CHEMBL583567
Phase Preclinical
Structure Type MOL
InChI Key ZLRZAKQLKHYLOI-FPQPQGOJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

720.7
MW (Da)
3.32
ALogP
8
HBA
5
HBD
158.3
PSA (Ų)
0.12
QED
1
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H50BrN5O7
MW 720.71
Aromatic Rings 2
Heavy Atoms 47
NP-Likeness -0.38

Activity Summary

Ki 1 meas. best 5.56

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
Ki 5.56 5.56 2755.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease Ki = 2755.0 nM 5.56 Inhibition of HIV1 protease expressed in Escherichia coli by fluorometric assay 19961222

Literature References

PubMed DOI Target Context # Activities
19961222 10.1021/jm901165g Protease 1
19961222 10.1021/jm901165g Human immunodeficiency virus 1 1
19961222 10.1021/jm901165g MT4 1

Data from ChEMBL 36 via Core Engine