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Compound Detail

CHEMBL4442340

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C[C@H](NC(=O)CCCCCCCCCCNC(=O)[C@]12CCC(C)(C)C[C@H]1C1=CC[C@@H]3[C@@]4(C)CC[C@H](OC(=O)c5ccccc5C(=O)O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)CC2)C(=O)O

Basic Information

ChEMBL ID CHEMBL4442340
Phase Preclinical
Structure Type MOL
InChI Key VBFFDKAIRMBTNY-WYRCATOASA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

859.2
MW (Da)
10.93
ALogP
6
HBA
4
HBD
159.1
PSA (Ų)
0.07
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C52H78N2O8
MW 859.20
Aromatic Rings 1
Heavy Atoms 62
NP-Likeness 1.48

Activity Summary

IC50 1 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 6.0 6.0 1000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 1000.0 nM 6.0 Inhibition of HIV1 protease expressed in Escherichia coli using Abz-Ala-Arg-Val-... 31617361

Literature References

PubMed DOI Target Context # Activities
31617361 10.1021/acs.jnatprod.9b00649 Protease 2

Data from ChEMBL 36 via Core Engine