carbonic anhydrase 7

Target id: 2749

Nomenclature: carbonic anhydrase 7

Family: 4.2.1.1 Carbonate dehydratases

Annotation status:  image of a grey circle Awaiting annotation/under development. Please contact us if you can help with annotation.  » Email us

   GtoImmuPdb view: OFF :     Currently no data for carbonic anhydrase 7 in GtoImmuPdb

Gene and Protein Information
Species TM AA Chromosomal Location Gene Symbol Gene Name Reference
Human - 264 16q22.1 CA7 carbonic anhydrase 7
Mouse - 264 8 D1 Car7 carbonic anhydrase 7
Rat - 264 19p14 Car7 carbonic anhydrase 7
Previous and Unofficial Names
carbonic anhydrase VII
Database Links
BRENDA
CATH/Gene3D
DrugBank Target
Ensembl Gene
Entrez Gene
GenitoUrinary Development Molecular Anatomy Project
Human Protein Atlas
KEGG Enzyme
KEGG Gene
OMIM
RefSeq Nucleotide
RefSeq Protein
SynPHARM
UniProtKB
Wikipedia
Enzyme Reaction
EC Number: 4.2.1.1

Download all structure-activity data for this target as a CSV file

Inhibitors
Key to terms and symbols View all chemical structures Click column headers to sort
Ligand Sp. Action Affinity Units Reference
ethoxzolamide Hs Inhibition 9.1 pKi 2
pKi 9.1 (Ki 8x10-10 M) [2]
topiramate Hs Inhibition 9.1 pKi 2
pKi 9.1 (Ki 9x10-10 M) [2]
methazolamide Hs Inhibition 8.7 pKi 2
pKi 8.7 (Ki 2.1x10-9 M) [2]
acetazolamide Hs Inhibition 8.6 pKi 1
pKi 8.6 (Ki 2.5x10-9 M) [1]
brinzolamide Hs Inhibition 8.6 pKi 2
pKi 8.6 (Ki 2.8x10-9 M) [2]
chlorthalidone Hs Inhibition 8.6 pKi 3
pKi 8.6 (Ki 2.8x10-9 M) [3]
dorzolamide Hs Inhibition 8.5 pKi 2
pKi 8.5 (Ki 3.5x10-9 M) [2]
zonisamide Hs Inhibition 6.9 pKi 2
pKi 6.9 (Ki 1.17x10-7 M) [2]
indisulam Hs Inhibition 6.9 pKi 2
pKi 6.9 (Ki 1.22x10-7 M) [2]
sulpiride Hs Inhibition 5.4 pKi 2
pKi 5.4 (Ki 3.63x10-6 M) [2]
Inhibitor Comments
Carbonic anhydrase (CA) inhibitors are active over a number of CA isozymes. We tag those isozymes with the highest drug affinity as the primary molecular target of each of the drugs, with the caveat that the drugs interact with other CA isozymes.

References

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1. Avvaru BS, Wagner JM, Maresca A, Scozzafava A, Robbins AH, Supuran CT, McKenna R. (2010) Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors. Bioorg. Med. Chem. Lett.20 (15): 4376-81. [PMID:20605094]

2. Sethi KK, Vullo D, Verma SM, Tanç M, Carta F, Supuran CT. (2013) Carbonic anhydrase inhibitors: synthesis and inhibition of the human carbonic anhydrase isoforms I, II, VII, IX and XII with benzene sulfonamides incorporating 4,5,6,7-tetrabromophthalimide moiety. Bioorg. Med. Chem.21 (19): 5973-82. [PMID:23965175]

3. Temperini C, Cecchi A, Scozzafava A, Supuran CT. (2009) Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference. Bioorg. Med. Chem.17 (3): 1214-21. [PMID:19119014]

How to cite this page

4.2.1.1 Carbonate dehydratases: carbonic anhydrase 7. Last modified on 30/03/2016. Accessed on 24/10/2017. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=2749.