Carbonic anhydrase inhibitors: purification and inhibition studies of pigeon (Columba livia var. domestica) red blood cell carbonic anhydrase with sulfonamides

被引:22
|
作者
Oezensoy, Oezen [1 ,2 ]
Arslan, Mikail [3 ]
Supuran, Claudiu T. [1 ]
机构
[1] Univ Florence, Lab Chim Bioinorgan, Dipartimento Chim, Sesto Fiorentino, Firenz, Italy
[2] Balikesir Univ, Sci & Art Fac, Dept Chem, Balikesir, Turkey
[3] Balikesir Univ, Susurluk Tech Vocat Sch Higher Educ, Balikesir, Turkey
关键词
Carbonic anhydrase; sulfonamide; pigeon; inhibitor; enzyme inhibition; PRESSURE LOWERING PROPERTIES; AROMATIC/HETEROCYCLIC SULFONAMIDES; HETEROCYCLIC SULFONAMIDES; THERAPEUTIC APPLICATIONS; IN-VITRO; ERYTHROCYTES; DERIVATIVES; ACID; RING; TAIL;
D O I
10.3109/14756366.2011.570759
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A carbonic anhydrase (CA, EC 4.2.1.1) from red blood cells of pigeons (Columba livia var. domestica), clCA, was purified to homogeneity. Its kinetic parameters for the CO(2) hydration reaction were measured. With a k(cat)/K(m) of 1.1 x 10(8) M (1) s (1), and a k(cat) of 1.3 x 10(6) s(-1), clCA has a high activity, similar to that of the human isoform hCA II. A group of 25 aromatic/heterocyclic sulfonamides incorporating the sulfanilamide, homosulfanilamide, benzene-1,3-disulfonamide, and acetazolamide scaffolds showed variable inhibitory activity against the pigeon enzyme, with K(I)s in the range of 1.9-3460 nM. Red blood cells of pigeons, like those of ostriches, contain thus just one CA isoform, unlike the blood of mammals, which normally contain two isoforms, one of low (CA I-like) and one of very high activity (CA II-like). However, from the sulfonamide inhibition viewpoint, the pigeon enzyme was more similar to hCA II than to the ostrich enzyme.
引用
收藏
页码:749 / 753
页数:5
相关论文
共 50 条
  • [21] Carbonic anhydrase contributes to red blood cell-mediated nitrite bioactivation
    Wajih, Nadeem
    Wang, Jun
    Basu, Swati
    Liu, Xiaohua
    Keggi, Christian
    Marvel, Madison
    Gladwin, Mark
    Kim-Shapiro, Daniel
    NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2014, 42 : 148 - 149
  • [22] Carbonic anhydrase inhibitors. Cloning, characterization and inhibition studies of the cytosolic isozyme III with anions
    Nishimori, Isao
    Minakuchi, Tomoko
    Onishi, Saburo
    Vullo, Daniela
    Cecchi, Alessandro
    Scozzafava, Andrea
    Supuran, Claudiu T.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2009, 24 (01) : 70 - 76
  • [23] Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5-and 6-sulfonamides
    Abdoli, Morteza
    Angeli, Andrea
    Bozdag, Murat
    Carta, Fabrizio
    Kakanejadifard, Ali
    Saeidian, Hamid
    Supuran, Claudiu T.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2017, 32 (01) : 1071 - 1078
  • [24] Carbonic Anhydrase Inhibition with Sulfonamides Incorporating Pyrazole- and Pyridazinecarboxamide Moieties Provides Examples of Isoform-Selective Inhibitors
    Angeli, Andrea
    Kartsev, Victor
    Petrou, Anthi
    Pinteala, Mariana
    Brovarets, Volodymyr
    Vydzhak, Roman
    Panchishin, Svitlana
    Geronikaki, Athina
    Supuran, Claudiu T.
    MOLECULES, 2021, 26 (22):
  • [25] Carbonic anhydrase inhibitors .36. Inhibition of isozymes I and II with Schiff bases derived from chalkones and aromatic/heterocyclic sulfonamides
    Supuran, CT
    Popescu, A
    Ilisiu, M
    Costandache, A
    Banciu, MD
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1996, 31 (06) : 439 - 447
  • [26] Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety
    Sethi, Kalyan K.
    Verma, Saurabh M.
    Tanc, Muhammet
    Carta, Fabrizio
    Supuran, Claudiu T.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (17) : 5168 - 5174
  • [27] Carbonic anhydrase inhibitors. Inhibition studies of the human secretory isoform VI with anions
    Nishimori, Isao
    Innocenti, Alessio
    Vullo, Daniela
    Scozzafava, Andrea
    Supuran, Claudiu T.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (04) : 1037 - 1042
  • [28] Carbonic anhydrase inhibitors: Inhibition of isozymes I, II and IV with heterocyclic mercaptans, sulfenamides, sulfonamides and their metal complexes
    Supuran, CT
    Scozzafava, A
    Saramet, I
    Banciu, MD
    JOURNAL OF ENZYME INHIBITION, 1998, 13 (03): : 177 - 194
  • [29] 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
    Sethi, Kalyan K.
    Vullo, Daniella
    Verma, Saurabh M.
    Tanc, Muhammet
    Carta, Fabrizio
    Supuran, Claudiu T.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (19) : 5973 - 5982
  • [30] Carbonic anhydrase inhibitors: the first QSAR study on inhibition of tumor-associated isoenzyme IX with aromatic and heterocyclic sulfonamides
    Jaiswal, M
    Khadikar, PV
    Scozzafava, A
    Supuran, CT
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (12) : 3283 - 3290