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Compound Detail

CHEMBL272190

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COC[C@H]1OC(=O)/C(=C/NC(C)(C)C)C2=C(O)C(=O)C3=C([C@H](OC(C)=O)C[C@]4(C)[C@@H](O)CC[C@@H]34)[C@]21C

Basic Information

ChEMBL ID CHEMBL272190
Phase Preclinical
Structure Type MOL
InChI Key YYEDILUQYWGXJC-VPWWIQQVSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

503.6
MW (Da)
2.64
ALogP
9
HBA
3
HBD
131.4
PSA (Ų)
0.39
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H37NO8
MW 503.59
Aromatic Rings 0
Heavy Atoms 36
NP-Likeness 2.09

Activity Summary

IC50 1 meas. best 4.39

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
LNCaP
CHEMBL612518
IC50 4.39 4.39 40700.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
LNCaP IC50 = 40700.0 nM 4.39 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