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Compound Detail

CHEMBL4172161

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C=C(C)[C@@H]1CC[C@]2(NCCN3CCC4(C3)CN(S(C)(=O)=O)C4)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12

Basic Information

ChEMBL ID CHEMBL4172161
Phase Preclinical
Structure Type MOL
InChI Key IIEJFABPLNTHRB-XQYUHJHPSA-N
1
Targets
3
Activities
1
Assay Types
2
PK Parameters
3
Publications
0
Known Names

Molecular Properties

746.1
MW (Da)
8.35
ALogP
5
HBA
2
HBD
90.0
PSA (Ų)
0.26
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C45H67N3O4S
MW 746.12
Aromatic Rings 1
Heavy Atoms 53
NP-Likeness 1.12

Activity Summary

EC50 3 meas. best 8.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 8.77 8.1067 1.7 3

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.0 hr Rattus norvegicus
T1/2 2.0 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
30067361 10.1021/acs.jmedchem.8b00854 Human immunodeficiency virus 1 3
30067361 10.1021/acs.jmedchem.8b00854 ADMET 2
30067361 10.1021/acs.jmedchem.8b00854 MT2 1

Data from ChEMBL 36 via Core Engine