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Compound Detail

CHEMBL1793818

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CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2cn(OC)c3ccccc23)NC(=O)[C@H](CCCCCP(=O)([O-])O)NC(=O)[C@H]2CCCCN2CC1=O.[K+]

Basic Information

ChEMBL ID CHEMBL1793818
Phase Preclinical
Structure Type BOTH
InChI Key DAZALYWLJRCDNR-SKNPYRJXSA-M
Parent Compound CHEMBL1852435
Active Moiety CHEMBL1852435
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

661.7
MW (Da)
1.92
ALogP
8
HBA
5
HBD
179.3
PSA (Ų)
0.18
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H47KN5O8P
MW 699.83
Aromatic Rings 2
Heavy Atoms 46
NP-Likeness 0.98

Activity Summary

IC50 1 meas. best 6.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histone deacetylase
CHEMBL2093865
IC50 6.75 6.75 180.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Histone deacetylase IC50 = 180.0 nM 6.75 Inhibitory activity against histone deacetylase (HDAC) derived from partially pu... 11206438

Literature References

PubMed DOI Target Context # Activities
11206438 10.1016/s0960-894x(00)00604-1 Histone deacetylase 1
11206438 10.1016/s0960-894x(00)00604-1 Plasmodium falciparum 1
11206438 10.1016/s0960-894x(00)00604-1 Eimeria tenella 1

Data from ChEMBL 36 via Core Engine