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Compound Detail

CHEMBL3126462

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CC1(C)CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](OC(=O)CCC(=O)O)[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1

Basic Information

ChEMBL ID CHEMBL3126462
Phase Preclinical
Structure Type MOL
InChI Key SCGXOHGFSYJCLH-GNKHBCFJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

662.9
MW (Da)
8.28
ALogP
6
HBA
2
HBD
110.1
PSA (Ų)
0.22
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H58O7
MW 662.91
Aromatic Rings 1
Heavy Atoms 48
NP-Likeness 2.38

Activity Summary

IC50 1 meas. best 4.81

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protease
CHEMBL2366517
IC50 4.81 4.81 15600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Protease IC50 = 15600.0 nM 4.81 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