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Compound Detail

CHEMBL333607

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Cc1ccc(CN2CCN(C[C@@H](O)C[C@@H](Cc3ccccc3)C(=O)NC3c4ccccc4C[C@H]3O)[C@H](C(=O)NC(C)(C)C)C2)cn1

Basic Information

ChEMBL ID CHEMBL333607
Phase Preclinical
Structure Type MOL
InChI Key FHGXAASKOJAWKN-GUFHCOKKSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names

Molecular Properties

627.8
MW (Da)
3.18
ALogP
7
HBA
4
HBD
118.0
PSA (Ų)
0.26
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H49N5O4
MW 627.83
Aromatic Rings 3
Heavy Atoms 46
NP-Likeness -0.44

Activity Summary

IC50 1 meas. best 9.21

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus type 1 protease
CHEMBL243
IC50 9.21 9.21 0.6 1

Pharmacokinetic Data

Parameter Value Units Species
Cmax - nM Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus type 1 protease IC50 = 0.62 nM 9.21 Inhibition of HIV-1 protease in vitro. 10978186

Literature References

PubMed DOI Target Context # Activities
10978186 10.1021/jm9903848 Human immunodeficiency virus type 1 protease 2
10978186 10.1021/jm9903848 No relevant target 2
10978186 10.1021/jm9903848 Canis familiaris 2

Data from ChEMBL 36 via Core Engine