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Compound Detail

CHEMBL1793984

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CCC(=O)CCCCC[C@@H]1NC(=O)[C@H]2CCCCN2C(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2c(-c3ccccc3)[nH]c3ccccc23)NC1=O

Basic Information

ChEMBL ID CHEMBL1793984
Phase Preclinical
Structure Type BOTH
InChI Key KDHIRMDJSXORPI-NHNPLKQTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

669.9
MW (Da)
5.20
ALogP
5
HBA
4
HBD
140.5
PSA (Ų)
0.20
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H51N5O5
MW 669.87
Aromatic Rings 3
Heavy Atoms 49
NP-Likeness 0.89

Activity Summary

IC50 1 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histone deacetylase
CHEMBL2093865
IC50 8.4 8.4 4.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
11206439 10.1016/s0960-894x(00)00605-3 Histone deacetylase 2
11206439 10.1016/s0960-894x(00)00605-3 Plasmodium falciparum 1
11206439 10.1016/s0960-894x(00)00605-3 Eimeria tenella 1

Data from ChEMBL 36 via Core Engine