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Compound Detail

CHEMBL5437394

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CC12C(=O)C(C)(C(c3ccccc3)=C1c1ccccc1)C1C(=O)N(CCCCN3CCN(c4ccccn4)CC3)C(=O)C12

Basic Information

ChEMBL ID CHEMBL5437394
Phase Preclinical
Structure Type MOL
InChI Key DLUWIXMSKRANKF-UHFFFAOYSA-N
13
Targets
13
Activities
3
Assay Types
0
PK Parameters
15
Publications
0
Known Names

Molecular Properties

574.7
MW (Da)
4.80
ALogP
6
HBA
0
HBD
73.8
PSA (Ų)
0.28
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H38N4O3
MW 574.73
Aromatic Rings 3
Heavy Atoms 43
NP-Likeness -0.70

Activity Summary

IC50 10 meas. best 5.08
Ki 2 meas. best 6.22
EC50 1 meas. best 6.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL4701
Ki 6.22 6.22 600.0 1
5-hydroxytryptamine receptor 1A
CHEMBL273
EC50 6.16 6.16 700.0 1
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 5.33 5.33 4700.0 1
HCT-116
CHEMBL394
IC50 5.08 5.08 8380.0 1
K562
CHEMBL385
IC50 5.05 5.05 8860.0 1
SW480
CHEMBL612544
IC50 4.92 4.92 12110.0 1
HepG2
CHEMBL395
IC50 4.84 4.84 14580.0 1
MDA-MB-231
CHEMBL400
IC50 4.82 4.82 15150.0 1
SW-620
CHEMBL612262
IC50 4.8 4.8 15990.0 1
A549
CHEMBL392
IC50 4.79 4.79 16060.0 1
PC-3
CHEMBL390
IC50 4.67 4.67 21160.0 1
HMEC-1
CHEMBL4296433
IC50 4.44 4.44 36580.0 1
D(2) dopamine receptor
CHEMBL339
IC50 4.3 4.3 50300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Histamine H1 receptor Ki = 600.0 nM 6.22 Displacement of [3H]pyrilamine from Sprague-Dawley rat H1 receptor assessed as i... 37951135
5-hydroxytryptamine receptor 1A EC50 = 700.0 nM 6.16 Agonist activity at Sprague-Dawley rat hippocampal membrane 5-HT1A receptor asse... 37951135
5-hydroxytryptamine receptor 2A Ki = 4700.0 nM 5.33 Displacement of [3H]ketanserin from Sprague-Dawley rat 5-HT2A receptor assessed ... 37951135
HCT-116 IC50 = 8380.0 nM 5.08 Cytotoxicity against human HCT-116 cells assessed as cell growth inhibition meas... 37951135
K562 IC50 = 8860.0 nM 5.05 Cytotoxicity against human K562 cells assessed as cell growth inhibition measure... 37951135
SW480 IC50 = 12110.0 nM 4.92 Cytotoxicity against human SW480 cells assessed as cell growth inhibition measur... 37951135
HepG2 IC50 = 14580.0 nM 4.84 Cytotoxicity against human HepG2 cells assessed as cell growth inhibition measur... 37951135
MDA-MB-231 IC50 = 15150.0 nM 4.82 Cytotoxicity against human MDA-MB-231 cells assessed as cell growth inhibition m... 37951135
SW-620 IC50 = 15990.0 nM 4.8 Cytotoxicity against human SW620 cells assessed as cell growth inhibition measur... 37951135
A549 IC50 = 16060.0 nM 4.79 Cytotoxicity against human A549 cells assessed as cell growth inhibition measure... 37951135
PC-3 IC50 = 21160.0 nM 4.67 Cytotoxicity against human PC-3 cells assessed as cell growth inhibition measure... 37951135
HMEC-1 IC50 = 36580.0 nM 4.44 Cytotoxicity against human HMEC-1 cells assessed as cell growth inhibition measu... 37951135
D(2) dopamine receptor IC50 = 50300.0 nM 4.3 Antagonist activity at Sprague-Dawley rat striatum membrane D2 receptor assessed... 37951135

Literature References

Data from ChEMBL 36 via Core Engine