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Compound Detail

CHEMBL4593419

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C[C@]12CC[C@H](OCc3ccccc3)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(n3cnc4ccccc43)=CC[C@@H]12
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL4593419
Phase Preclinical
Structure Type MOL
InChI Key NXQFSRYKPZJBHF-VJPGGQIVSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

478.7
MW (Da)
8.04
ALogP
3
HBA
0
HBD
27.1
PSA (Ų)
0.35
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H38N2O
MW 478.68
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness 0.74

Activity Summary

IC50 2 meas. best 5.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
CWR22R
CHEMBL612657
 IC50 5.92 5.92 1200.0 1
LNCaP
CHEMBL612518
 IC50 5.29 5.29 5120.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
CWR22R IC50 = 1200.0 nM 5.92 Antiproliferative activity against human CWR22Rv1 cells after 7 days by MTT assa... 27437082
LNCaP IC50 = 5120.0 nM 5.29 Antiproliferative activity against human LNCAP cells after 7 days by MTT assay 27437082

Literature References

PubMed DOI Target Context # Activities
27437082 10.1021/acsmedchemlett.6b00137 Androgen receptor 1
27437082 10.1021/acsmedchemlett.6b00137 Steroid 17-alpha-hydroxylase/17,20 lyase 1
27437082 10.1021/acsmedchemlett.6b00137 LNCaP 1
27437082 10.1021/acsmedchemlett.6b00137 CWR22R 1

Data from ChEMBL 36 via Core Engine