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Structural basis for the interaction between carbonic anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F11%3A00365071" target="_blank" >RIV/61388963:_____/11:00365071 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/11:00365071

  • Result on the web

    <a href="http://dx.doi.org/10.1021/jm2000213" target="_blank" >http://dx.doi.org/10.1021/jm2000213</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/jm2000213" target="_blank" >10.1021/jm2000213</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Structural basis for the interaction between carbonic anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides

  • Original language description

    lsoquinolinesulfonamides inhibit human carbonic anhydrases (hCAs) and display selectivity toward therapeutically relevant isozymes. The crystal structure of hCA 11 in complex with 6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamide revealed unusual inhibitor binding. Structural analyses allowed for discerning the fine details of the inhibitor binding mode to the active site, thus providing clues for the future design of even more selective inhibitors for druggable isoforms such as the cancer associated hCA IX and neuronal hCA VII.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA203%2F09%2F0820" target="_blank" >GA203/09/0820: Structure based drug design of specific nucleotidases inhibitors, potentially pharmacologically important compounds.</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Medicinal Chemistry

  • ISSN

    0022-2623

  • e-ISSN

  • Volume of the periodical

    54

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    5

  • Pages from-to

    2522-2526

  • UT code for WoS article

    000289215700048

  • EID of the result in the Scopus database