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Compound Detail

CHEMBL5196278

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Cc1nc2c(F)cc(-c3nc(Nc4ccc(Sc5cnc(N6CCC7(CC6)CO[C@@H](C)[C@H]7N)cn5)c(Cl)n4)ncc3F)cc2n1C(C)C

Basic Information

ChEMBL ID CHEMBL5196278
Phase Preclinical
Structure Type MOL
InChI Key IRHJVBAWASTUSE-YVGXBJCXSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

693.2
MW (Da)
6.73
ALogP
12
HBA
2
HBD
132.8
PSA (Ų)
0.18
QED
3
Ro5 Violations
7
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H35ClF2N10OS
MW 693.23
Aromatic Rings 5
Heavy Atoms 48
NP-Likeness -1.04

Activity Summary

IC50 1 meas. best 6.86

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
CDK4/Cyclin D3
CHEMBL3038472
IC50 6.86 6.86 139.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
CDK4/Cyclin D3 IC50 = 139.3 nM 6.86 Inhibition of recombinant N-terminal GST/His6-fusion tagged human CDK4/Cyclin D3... 35447031

Literature References

PubMed DOI Target Context # Activities
35447031 10.1021/acs.jmedchem.2c00063 Tyrosine-protein phosphatase non-receptor type 11 1
35447031 10.1021/acs.jmedchem.2c00063 CDK4/Cyclin D3 1

Data from ChEMBL 36 via Core Engine