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Compound Detail

CHEMBL435007

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CO[C@H]1C[C@H](C)CC2=C(NC(C)C)C(=O)C=C(NC(=O)/C(C)=C/C=C\[C@H](OC)[C@@H](OC(N)=O)/C(C)=C/[C@H](C)/C1=N/O)C2=O

Basic Information

ChEMBL ID CHEMBL435007
Phase Preclinical
Structure Type MOL
InChI Key ALUHWHWCGADXIZ-LMDJLJKTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

600.7
MW (Da)
3.23
ALogP
10
HBA
4
HBD
178.6
PSA (Ų)
0.16
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H44N4O8
MW 600.71
Aromatic Rings 0
Heavy Atoms 43
NP-Likeness 1.99

Activity Summary

IC50 1 meas. best 6.57

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
SK-BR-3
CHEMBL613834
IC50 6.57 6.57 270.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
SK-BR-3 IC50 = 270.0 nM 6.57 In vitro inhibition of p185 erbB-2 oncoprotein in human breast cancer SK-BR-3 ce... 7562912

Literature References

PubMed DOI Target Context # Activities
7562912 10.1021/jm00019a011 SK-BR-3 1

Data from ChEMBL 36 via Core Engine