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Compound Detail

CHEMBL4521631

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CC(C)(CC(=O)O)CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@H]5CC(C)(C)CC[C@]5(C(=O)NCCCCCC(=O)O)CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C

Basic Information

ChEMBL ID CHEMBL4521631
Phase Preclinical
Structure Type MOL
InChI Key DPKPXPPZJCKBBH-BXSQRKAGSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

712.0
MW (Da)
9.35
ALogP
5
HBA
3
HBD
130.0
PSA (Ų)
0.10
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H69NO7
MW 712.03
Aromatic Rings 0
Heavy Atoms 51
NP-Likeness 2.10

Activity Summary

IC50 1 meas. best 4.91

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 4.91 4.91 12400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 12400.0 nM 4.91 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 1

Data from ChEMBL 36 via Core Engine