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Compound Detail

CHEMBL452768

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O=C(O[C@H]1CN[C@H](C#Cc2cc3ncnc(Nc4ccc5c(ccn5S(=O)(=O)c5ccsc5)c4)c3s2)C1)N1CCOCC1

Basic Information

ChEMBL ID CHEMBL452768
Phase Preclinical
Structure Type MOL
InChI Key HAYQBGMCBFKTMA-IFMALSPDSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

634.8
MW (Da)
4.24
ALogP
12
HBA
2
HBD
127.7
PSA (Ų)
0.27
QED
2
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H26N6O5S3
MW 634.77
Aromatic Rings 5
Heavy Atoms 43
NP-Likeness -1.24

Activity Summary

IC50 4 meas. best 6.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Receptor tyrosine-protein kinase erbB-2
CHEMBL1824
IC50 6.92 6.92 120.0 1
BT-474
CHEMBL614529
IC50 6.92 6.92 120.0 1
Epidermal growth factor receptor
CHEMBL203
IC50 6.82 6.82 150.0 1
HN5
CHEMBL614828
IC50 6.2 6.2 630.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19208477 10.1016/j.bmcl.2009.01.080 Epidermal growth factor receptor 2
19208477 10.1016/j.bmcl.2009.01.080 HN5 1
19208477 10.1016/j.bmcl.2009.01.080 BT-474 1
19208477 10.1016/j.bmcl.2009.01.080 Receptor tyrosine-protein kinase erbB-2 1
19208477 10.1016/j.bmcl.2009.01.080 HFF 1

Data from ChEMBL 36 via Core Engine