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Compound Detail

CHEMBL3126457

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

Basic Information

ChEMBL ID CHEMBL3126457
Phase Preclinical
Structure Type MOL
InChI Key NEUMQEXVNPTVQU-HQHCPXFPSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

757.0
MW (Da)
9.09
ALogP
7
HBA
3
HBD
164.5
PSA (Ų)
0.14
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H68O10
MW 757.02
Aromatic Rings 0
Heavy Atoms 54
NP-Likeness 2.29

Activity Summary

IC50 1 meas. best 4.56

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 4.56 4.56 27500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 27500.0 nM 4.56 Inhibition of HIV1 recombinant protease expressed in Escherichia coli using Abz-... 24480359

Literature References

PubMed DOI Target Context # Activities
24480359 10.1016/j.ejmech.2013.12.049 Protease 1

Data from ChEMBL 36 via Core Engine