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Compound Detail

CHEMBL4210691

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CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@H]5CC(C)(C)CC[C@]5(C(=O)N(CC(=O)NC(C)(C)C)Cc5cccc(F)c5)CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C

Basic Information

ChEMBL ID CHEMBL4210691
Phase Preclinical
Structure Type MOL
InChI Key AJGNDJWOJKJAPB-JNNZJYSRSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

719.0
MW (Da)
9.80
ALogP
4
HBA
1
HBD
75.7
PSA (Ų)
0.23
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C45H67FN2O4
MW 719.04
Aromatic Rings 1
Heavy Atoms 52
NP-Likeness 1.29

Activity Summary

EC50 1 meas. best 4.98

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
A2780
CHEMBL614004
EC50 4.98 4.98 10400.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
A2780 EC50 = 10400.0 nM 4.98 Cytotoxicity against human A2780 cells after 96 hrs by sulforhodamine-B assay 29529499

Literature References

Data from ChEMBL 36 via Core Engine