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Compound Detail

CHEMBL8404

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CC[C@@H]1/C=C(\C)C[C@H](C)C[C@H](OC)[C@H]2O[C@@](O)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@H](/C(C)=C/[C@@H]3CC[C@@H](Oc4cccc(O)c4)[C@H](OC)C3)[C@H](C)[C@@H](O)CC1=O)[C@H](C)C[C@@H]2OC

Basic Information

ChEMBL ID CHEMBL8404
Phase Preclinical
Structure Type MOL
InChI Key APDFWCQXDRHKGD-JTHPELDASA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

884.1
MW (Da)
6.27
ALogP
13
HBA
3
HBD
187.6
PSA (Ų)
0.15
QED
3
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C49H73NO13
MW 884.12
Aromatic Rings 1
Heavy Atoms 63
NP-Likeness 1.26

Activity Summary

IC50 1 meas. best 8.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Murine T-cell line
CHEMBL614766
IC50 8.77 8.77 1.7 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Murine T-cell line IC50 = 1.7 nM 8.77 Inhibition of proliferation of PMA and Ionomycin stimulated murine T cells -

Literature References

PubMed DOI Target Context # Activities
- 10.1016/0960-894X(95)00161-L Murine T-cell line 1

Data from ChEMBL 36 via Core Engine