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Compound Detail

CHEMBL430288

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CC1=C(CCC(=O)O)c2cc3[nH]c(cc4[nH]c(cc5nc(cc1n2)C(CCC(=O)O)=C5CC(=O)O)c(CCC(=O)O)c4CC(=O)O)c(CCC(=O)O)c3CC(=O)O

Basic Information

ChEMBL ID CHEMBL430288
Phase Preclinical
Structure Type MOL
InChI Key NIGVICSDLYHPTO-YBWGHNILSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

786.8
MW (Da)
4.65
ALogP
9
HBA
9
HBD
318.5
PSA (Ų)
0.08
QED
2
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H38N4O14
MW 786.75
Aromatic Rings 3
Heavy Atoms 57
NP-Likeness 0.12

Activity Summary

EC50 2 meas. best 4.97

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 4.97 4.97 10724.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus 1 EC50 = 10724.0 nM 4.97 Inhibition of HIV-1 P24 production. 8164251

Literature References

PubMed DOI Target Context # Activities
8164251 10.1021/jm00034a007 Human immunodeficiency virus 1 2

Data from ChEMBL 36 via Core Engine