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Compound Detail

CHEMBL420572

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Cc1c2cc(c(C)[n+]1-c1ccc(S(=O)(=O)Nc3nnc(S(N)(=O)=O)s3)cc1)CCCCCCCCC2.[O-][Cl+3]([O-])([O-])[O-]

Basic Information

ChEMBL ID CHEMBL420572
Phase Preclinical
Structure Type MOL
InChI Key UTVSLTWGWRNBMS-UHFFFAOYSA-M
Parent Compound CHEMBL1185544
Active Moiety CHEMBL1185544
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

550.8
MW (Da)
3.71
ALogP
7
HBA
2
HBD
136.0
PSA (Ų)
0.46
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 C24H32ClN5O8S3
MW 650.20
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -1.14

Activity Summary

Ki 4 meas. best 8.86

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Carbonic anhydrase 2
CHEMBL205
Ki 8.86 8.86 1.4 1
Carbonic anhydrase 1
CHEMBL261
Ki 8.52 8.52 3.0 1
Carbonic anhydrase 4
CHEMBL281
Ki 8.34 8.34 4.6 1
Carbonic anhydrase 9
CHEMBL3594
Ki 7.92 7.92 12.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15084132 10.1021/jm031079w Unchecked 6
15084132 10.1021/jm031079w Carbonic anhydrase 1 1
15084132 10.1021/jm031079w Carbonic anhydrase 2 1
15084132 10.1021/jm031079w Carbonic anhydrase 4 1
15084132 10.1021/jm031079w Carbonic anhydrase 9 1
15084132 10.1021/jm031079w Homo sapiens 1

Data from ChEMBL 36 via Core Engine