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

CHEMBL4782954

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
CS(=O)(=O)c1c(C#N)ccc2c(-c3nc(N[C@H]4CCCNC4)ncc3C(F)(F)F)c[nH]c12
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL4782954
Phase Preclinical
Structure Type MOL
InChI Key DGAWYBIEBJUVHR-LBPRGKRZSA-N
5
Targets
8
Activities
3
Assay Types
3
PK Parameters
7
Publications
0
Known Names

Molecular Properties

464.5
MW (Da)
3.08
ALogP
7
HBA
3
HBD
123.6
PSA (Ų)
0.54
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H19F3N6O2S
MW 464.47
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -1.15

Activity Summary

IC50 6 meas. best 7.48
EC50 1 meas. best 7.82
Kd 1 meas. best 10.1

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cyclin-dependent kinase 7/ cyclin H
CHEMBL2111288
 Kd 10.1 10.1 0.1 1
HCC70
CHEMBL1075461
 EC50 7.82 7.82 15.0 1
CDK12/Cyclin K
CHEMBL4106169
 IC50 7.48 7.09 33.0 2
CDK9/cyclin T1
CHEMBL2111389
 IC50 7.22 6.96 60.0 2
Cyclin-dependent kinase 2/cyclin E1
CHEMBL1907605
 IC50 6.7 6.625 200.0 2

Pharmacokinetic Data

Parameter Value Units Species
CL 368.0 mL.min-1.kg-1 Mus musculus
CL 38.0 mL.min-1.kg-1 Mus musculus
F 5.0 % Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cyclin-dependent kinase 7/ cyclin H Kd = 0.08 nM 10.1 Binding affinity to full length CDK7 (1 to 346 residues) /N-terminal TEV cleavab... 34726887
HCC70 EC50 = 15.0 nM 7.82 Antiproliferative activity against human HCC70 cells incubated for 72 hrs by Cel... 34726887
CDK12/Cyclin K IC50 = 33.0 nM 7.48 Inhibition of CDK12/cyclin K (unknown origin) using 5-FAM-labeled peptide as sub... 34726887
CDK9/cyclin T1 IC50 = 60.0 nM 7.22 Inhibition of CDK9/cyclin T1 (unknown origin) using 5-FAM-labeled peptide as sub... 34726887
Cyclin-dependent kinase 2/cyclin E1 IC50 = 200.0 nM 6.7 Inhibition of CDK2/Cyclin E (unknown origin) using 5-FAM-CDK7tide substrate incu... -
CDK12/Cyclin K IC50 = 200.0 nM 6.7 Inhibition of CDK12 (686 to 1082 residues) /Cyclin K (unknown origin) using 5-FA... -
CDK9/cyclin T1 IC50 = 200.0 nM 6.7 Inhibition of CDK9/Cyclin T1 (unknown origin) using 5-FAM-CDK9tide peptide subst... -
Cyclin-dependent kinase 2/cyclin E1 IC50 = 284.0 nM 6.55 Inhibition of CDK2/cyclin E1 (unknown origin) using 5-FAM-labeled peptide as sub... 34726887

Literature References

PubMed DOI Target Context # Activities
34726887 10.1021/acs.jmedchem.1c01171 ADMET 4
34726887 10.1021/acs.jmedchem.1c01171 No relevant target 1
34726887 10.1021/acs.jmedchem.1c01171 Cyclin-dependent kinase 2/cyclin E1 1
34726887 10.1021/acs.jmedchem.1c01171 HCC70 1
34726887 10.1021/acs.jmedchem.1c01171 Cyclin-dependent kinase 7/ cyclin H 1
34726887 10.1021/acs.jmedchem.1c01171 CDK9/cyclin T1 1
34726887 10.1021/acs.jmedchem.1c01171 CDK12/Cyclin K 1

Data from ChEMBL 36 via Core Engine