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Compound Detail

CHEMBL304805

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CC(C)C[C@@]1(C2=C(O)[C@](Cc3ccccc3)(C[C@H](O)[C@H](Cc3ccccc3)NC(=O)O[C@@H]3CCOC3)N=C2)N=CC([C@@H](Cc2ccccc2)C(N)=O)=C1O

Basic Information

ChEMBL ID CHEMBL304805
Phase Preclinical
Structure Type MOL
InChI Key JFKGJMRTAQFDCR-AYQUJQEASA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

734.9
MW (Da)
5.77
ALogP
9
HBA
5
HBD
176.1
PSA (Ų)
0.12
QED
2
Ro5 Violations
16
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H50N4O7
MW 734.89
Aromatic Rings 3
Heavy Atoms 54
NP-Likeness 0.49

Activity Summary

IC50 1 meas. best 8.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus type 1 protease
CHEMBL243
IC50 8.89 8.89 1.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus type 1 protease IC50 = 1.3 nM 8.89 In vitro inhibitory concentration against HIV-1 protease 8295206

Literature References

PubMed DOI Target Context # Activities
8295206 10.1021/jm00028a001 Human immunodeficiency virus type 1 protease 2

Data from ChEMBL 36 via Core Engine