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DraconiticBiochemistryBiomolecules · Catabolism · Biosynthesis · Metabolism
Data

CA7 · ChEMBL activity 2456868

Kinact source measurement: = 5.73 uM. No cross-assay comparison is prequalified.

Assay activity2456868In this release

Source assertion

ChEMBL direct single-protein activity record with source-reported and source-standardized lexical values preserved.
Evidence ID
ACTIVITY:ChEMBL_37:2456868
Subject dossier
ca7
Source chain
uniprot + chembl
Upstream record
2456868
Corpus snapshot
2026-07-14T09:23:31Z
Admission status
In this release

Lossless activity measurement

Source-reported value
= 5.73 uM
Source-standardized value
= 5.73 uM
Reported endpoint
Kinact
Standardized endpoint
Kinact
Reported upper bound
not reported by the source
Reported text value
not reported by the source
Standardization flag
0
pChEMBL from source
not reported by the source

Reported and source-standardized fields are displayed separately and retain their exact lexical values. The standardized field does not overwrite the upstream report.

Not comparable with other recordsCONDITION_MISSING

No cross-assay comparison is authorized by this record. Evaluate target, construct, endpoint, relation, units, assay format, conditions, and exact molecular form first.

Assay and target

ChEMBL activity
2456868
Target
CHEMBL2326, SINGLE PROTEIN
Assay
CHEMBL1022728, Binding (B)
BAO format
BAO_0000357, single protein format
BAO endpoint
BAO_0000179
Target confidence
9, Direct single protein target assigned
Source quality flags
potential_duplicate=0; data_validity_comment=not reported by the source
Upstream assay description

Inhibition of human recombinant carbonic anhydrase 7 by stopped flow CO2 hydration method

Compound identity

Molecule
CHEMBL442687, TIOXOLONE
Parent form
CHEMBL442687; is_parent_form=true
Molecule type
Small molecule
Chirality source code
2
Standard InChIKey
SLYPOVJCSQHITR-UHFFFAOYSA-N
Canonical SMILES
O=c1oc2cc(O)ccc2s1
Standard InChI
InChI=1S/C7H4O3S/c8-4-1-2-6-5(3-4)10-7(9)11-6/h1-3,8H

Document

Carbonic anhydrase inhibitors: thioxolone versus sulfonamides for obtaining isozyme-selective inhibitors?

Innocenti A, Maresca A, Scozzafava A, Supuran CT.

ChEMBL document
CHEMBL1155067
Journal / year
Bioorg Med Chem Lett, 2008
PubMed
18572406

Comparison state

Prequalified
No — pairwise evaluation is still required
Protein identity
P43166, taxon 9606
Variant / construct
not reported by the source / not reported by the source
Conditions
pH not reported by the source; temperature not reported by the source °C; substrate not reported by the source; buffer not reported by the source

Snapshot provenance

Each row is a source snapshot this record was built from: when it was retrieved, its path and SHA-256 digest, and the exact request. The snapshot files stay with the build and are not served here. These rows document this record; they are not general citations.

RetrievedSnapshotSHA-256Upstream request
2026-07-14T09:21:32Zraw/uniprot/entries/P43166.jsondc0ec23dc5d7dfcf4737e905d75df89f664cdb3e05519fcfef79fbaf218da84fOpen exact source
2026-07-14T09:22:19Zraw/chembl/targets/CHEMBL2326.json62691ca1f8537e95ebb7067dc86d7bc8dc2258b418c22d6317910ba5c87d371bOpen exact source
2026-07-14T09:22:38Zraw/chembl/direct-assays/CHEMBL2326.jsonf0238fb298d0c0e9bc652a3268f81791d92dc1c422ccc9a447278e125104c829Open exact source
2026-07-14T09:23:01Zraw/chembl/assay-activities/CHEMBL1022728.json77363b0cbb9802f7fcdf45ca1e241e2352ee46426e8d90500cefdda07583b9feOpen exact source
2026-07-14T09:23:26Zraw/chembl/activities/2456868.json41a505781651b0eaea8989194f3c731ceddf55f0b85b2f74e3f41a775b36d761Open exact source
2026-07-14T09:23:26Zraw/chembl/assays/CHEMBL1022728.json07d3b2644d8b9cf7ca594b4c490bc1a62f8363392f734f5dcbbb132f0e4e1a17Open exact source
2026-07-14T09:23:19Zraw/chembl/molecules/CHEMBL442687.jsonf152b44651db17cb570a3d901bba045a331eebd01e4fac702cecfbf64650aa99Open exact source
2026-07-14T09:23:19Zraw/chembl/documents/CHEMBL1155067.jsona852cdb1b30571a0f6ed5def67b2c61a1b73e56c6483dd07330b61bc3a77e725Open exact source