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7JNX

Carbonic Anhydrase II Complexed with N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)pivalamide

Summary for 7JNX
Entry DOI10.2210/pdb7jnx/pdb
DescriptorCarbonic anhydrase 2, GLYCEROL, ZINC ION, ... (6 entities in total)
Functional Keywordscarbonic anhydrase, ca inhibitor, structure guided drug design, carbonic anhydrase ii, carbonic anhydrase ix, caii, caix, sulfonamide, lyase, lyase-inhibitor complex, lyase/inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight29789.02
Authors
Andring, J.T.,McKenna, R. (deposition date: 2020-08-05, release date: 2020-11-04, Last modification date: 2023-10-18)
Primary citationAndring, J.T.,Fouch, M.,Akocak, S.,Angeli, A.,Supuran, C.T.,Ilies, M.A.,McKenna, R.
Structural Basis of Nanomolar Inhibition of Tumor-Associated Carbonic Anhydrase IX: X-Ray Crystallographic and Inhibition Study of Lipophilic Inhibitors with Acetazolamide Backbone.
J.Med.Chem., 63:13064-13075, 2020
Cited by
PubMed Abstract: This study provides a structure-activity relationship study of a series of lipophilic carbonic anhydrase (CA) inhibitors with an acetazolamide backbone. The inhibitors were tested against the tumor-expressed CA isozyme IX (CA IX), and the cytosolic CA I, CA II, and membrane-bound CA IV. The study identified several low nanomolar potent inhibitors against CA IX, with lipophilicities spanning two log units. Very potent pan-inhibitors with nanomolar potency against CA IX and sub-nanomolar potency against CA II and CA IV, and with potency against CA I one order of magnitude better than the parent acetazolamide were also identified in this study, together with compounds that displayed selectivity against membrane-bound CA IV. A comprehensive X-ray crystallographic study (12 crystal structures), involving both CA II and a soluble CA IX mimetic (CA IX-mimic), revealed the structural basis of this particular inhibition profile and laid the foundation for further developments toward more potent and selective inhibitors for the tumor-expressed CA IX.
PubMed: 33085484
DOI: 10.1021/acs.jmedchem.0c01390
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.286 Å)
Structure validation

237735

數據於2025-06-18公開中

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