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Compound Detail

CHEMBL4162920

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CCC(C)NCC(O)COc1ccc(C(=O)NCCc2ccc(S(N)(=O)=O)cc2)cc1.Cl

Basic Information

ChEMBL ID CHEMBL4162920
Phase Preclinical
Structure Type MOL
InChI Key HCFVUMHBJGFRDI-UHFFFAOYSA-N
Parent Compound CHEMBL4302442
Active Moiety CHEMBL4302442
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

449.6
MW (Da)
1.43
ALogP
6
HBA
4
HBD
130.8
PSA (Ų)
0.39
QED
0
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H32ClN3O5S
MW 486.03
Aromatic Rings 2
Heavy Atoms 31
NP-Likeness -1.11

Activity Summary

Ki 4 meas. best 8.55

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Carbonic anhydrase 12
CHEMBL3242
Ki 8.55 8.55 2.8 1
Carbonic anhydrase 1
CHEMBL261
Ki 7.34 7.34 45.8 1
Carbonic anhydrase 9
CHEMBL3594
Ki 7.27 7.27 53.6 1
Carbonic anhydrase 2
CHEMBL205
Ki 7.25 7.25 55.7 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29851481 10.1021/acs.jmedchem.8b00625 Carbonic anhydrase 2 1
29851481 10.1021/acs.jmedchem.8b00625 Carbonic anhydrase 1 1
29851481 10.1021/acs.jmedchem.8b00625 Carbonic anhydrase 9 1
29851481 10.1021/acs.jmedchem.8b00625 Carbonic anhydrase 12 1
29851481 10.1021/acs.jmedchem.8b00625 Beta-1 adrenergic receptor 1
29851481 10.1021/acs.jmedchem.8b00625 Beta-2 adrenergic receptor 1

Data from ChEMBL 36 via Core Engine