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Compound Detail

CHEMBL3120770

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CCOc1cc(O[C@@H]2C[C@H]3C(=O)N[C@]4(C(=O)NS(=O)(=O)C5CC5)C[C@H]4/C=C\CCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N3C2)c2ccc(OC)c(C)c2n1

Basic Information

ChEMBL ID CHEMBL3120770
Phase Preclinical
Structure Type MOL
InChI Key YIGLMNQRVNZRQM-AXOKOONASA-N
1
Targets
3
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names

Molecular Properties

783.9
MW (Da)
4.20
ALogP
11
HBA
3
HBD
191.6
PSA (Ų)
0.31
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H53N5O10S
MW 783.94
Aromatic Rings 2
Heavy Atoms 55
NP-Likeness -0.09

Activity Summary

EC50 3 meas. best 9.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Hepatitis C virus
CHEMBL379
EC50 9.4 8.05 0.4 3

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.3667 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23506530 10.1021/jm400121t Hepatitis C virus 3
23506530 10.1021/jm400121t Caco-2 1
23506530 10.1021/jm400121t Liver microsome 1

Data from ChEMBL 36 via Core Engine