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Compound Detail

CHEMBL4171833

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C=C(C)[C@@H]1CC[C@]2(NCCN3CCCS(=O)(=O)CC3)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 CHEMBL4171833
Phase Preclinical
Structure Type MOL
InChI Key MSDHATIOJPHQQX-FJMUSEAASA-N
1
Targets
2
Activities
1
Assay Types
2
PK Parameters
3
Publications
0
Known Names

Molecular Properties

705.1
MW (Da)
8.50
ALogP
5
HBA
2
HBD
86.7
PSA (Ų)
0.28
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 C43H64N2O4S
MW 705.06
Aromatic Rings 1
Heavy Atoms 50
NP-Likeness 1.12

Activity Summary

EC50 2 meas. best 8.44

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 8.44 7.95 3.6 2

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