Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL500328

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CC(=O)OC[C@H]1O[C@@H](NC(=O)c2ccc(NC(=O)CCCc3ccc(N(CCCl)CCCl)cc3)cc2)[C@H](F)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL500328
Phase Preclinical
Structure Type MOL
InChI Key XCVMYLVPWUDQGV-GJQHGMRUSA-N
9
Targets
13
Activities
1
Assay Types
0
PK Parameters
14
Publications
0
Known Names

Molecular Properties

712.6
MW (Da)
4.15
ALogP
10
HBA
2
HBD
149.6
PSA (Ų)
0.15
QED
1
Ro5 Violations
16
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H40Cl2FN3O9
MW 712.60
Aromatic Rings 2
Heavy Atoms 48
NP-Likeness -0.03

Activity Summary

IC50 13 meas. best 6.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
PA-1
CHEMBL614949
 IC50 6.52 6.52 300.0 2
PC-3
CHEMBL390
 IC50 5.85 5.85 1400.0 2
A549
CHEMBL392
 IC50 5.57 5.57 2700.0 2
DLD-1
CHEMBL614285
 IC50 5.52 5.52 3000.0 1
Fibroblast
CHEMBL5314315
 IC50 5.4 5.4 4000.0 1
ADMET
CHEMBL612558
 IC50 5.4 5.4 4000.0 1
MCF7
CHEMBL387
 IC50 5.3 5.3 5000.0 2
NON-PROTEIN TARGET
CHEMBL3879801
 IC50 5.16 5.16 7000.0 1
M4Beu cell line
CHEMBL612270
 IC50 5.16 5.16 7000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
PA-1 IC50 = 300.0 nM 6.52 Cytotoxicity against human PA1 cells by resazurin reduction test 18424156
PA-1 IC50 = 300.0 nM 6.52 Cytotoxicity against human PA1 assessed as inhibition of cell growth incubated f... 28927903
PC-3 IC50 = 1400.0 nM 5.85 Cytotoxicity against human PC3 cells by resazurin reduction test 18424156
PC-3 IC50 = 1400.0 nM 5.85 Cytotoxicity against human PC3 assessed as inhibition of cell growth incubated f... 28927903
A549 IC50 = 2700.0 nM 5.57 Cytotoxicity against human A549 cells by resazurin reduction test 18424156
A549 IC50 = 2700.0 nM 5.57 Cytotoxicity against human A549 assessed as inhibition of cell growth incubated ... 28927903
DLD-1 IC50 = 3000.0 nM 5.52 Cytotoxicity against human DLD1 cells by resazurin reduction test 18424156
ADMET IC50 = 4000.0 nM 5.4 Cytotoxicity against human primary fibroblasts by resazurin reduction test 18424156
Fibroblast IC50 = 4000.0 nM 5.4 Cytotoxicity against human fibroblasts assessed as inhibition of cell growth inc... 28927903
MCF7 IC50 = 5000.0 nM 5.3 Cytotoxicity against human MCF7 cells by resazurin reduction test 18424156
MCF7 IC50 = 5000.0 nM 5.3 Cytotoxicity against human MCF7 assessed as inhibition of cell growth incubated ... 28927903
NON-PROTEIN TARGET IC50 = 7000.0 nM 5.16 Cytotoxicity against human M4Beu cells by resazurin reduction test 18424156
M4Beu cell line IC50 = 7000.0 nM 5.16 Cytotoxicity against human M4Beu assessed as inhibition of cell growth incubated... 28927903

Literature References

PubMed DOI Target Context # Activities
18424156 10.1016/j.bmc.2008.03.038 L929 3
18424156 10.1016/j.bmc.2008.03.038 ADMET 1
18424156 10.1016/j.bmc.2008.03.038 PC-3 1
18424156 10.1016/j.bmc.2008.03.038 MCF7 1
18424156 10.1016/j.bmc.2008.03.038 A549 1
18424156 10.1016/j.bmc.2008.03.038 DLD-1 1
18424156 10.1016/j.bmc.2008.03.038 NON-PROTEIN TARGET 1
18424156 10.1016/j.bmc.2008.03.038 PA-1 1
28927903 10.1016/j.bmc.2017.08.043 Fibroblast 1
28927903 10.1016/j.bmc.2017.08.043 PC-3 1
28927903 10.1016/j.bmc.2017.08.043 MCF7 1
28927903 10.1016/j.bmc.2017.08.043 A549 1
28927903 10.1016/j.bmc.2017.08.043 M4Beu cell line 1
28927903 10.1016/j.bmc.2017.08.043 PA-1 1

Data from ChEMBL 36 via Core Engine