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Compound Detail

CHEMBL271191

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CCN/C=C1/C(=O)O[C@H](COC)[C@@]2(C)C1=C(O)C(=O)C1=C2[C@H](OC(C)=O)C[C@]2(C)[C@@H](O)CC[C@@H]12

Basic Information

ChEMBL ID CHEMBL271191
Phase Preclinical
Structure Type MOL
InChI Key NCHYTWNAUIQXAH-ZYPCNODZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

475.5
MW (Da)
1.86
ALogP
9
HBA
3
HBD
131.4
PSA (Ų)
0.40
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H33NO8
MW 475.54
Aromatic Rings 0
Heavy Atoms 34
NP-Likeness 2.24

Activity Summary

IC50 1 meas. best 5.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
LNCaP
CHEMBL612518
IC50 5.15 5.15 7067.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
LNCaP IC50 = 7067.0 nM 5.15 Growth inhibition of human LNCap cells 18269228

Literature References

PubMed DOI Target Context # Activities
18269228 10.1021/jm7012858 Serine/threonine-protein kinase mTOR 1
18269228 10.1021/jm7012858 LNCaP 1
18269228 10.1021/jm7012858 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform 1

Data from ChEMBL 36 via Core Engine