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
  • [31] Sulfonamides containing curcumin scaffold: Synthesis, characterization, carbonic anhydrase inhibition and molecular docking studies
    Ahmed, Mahmood
    Qadir, Muhammad Abdul
    Hameed, Abdul
    Arshad, Muhammad Nadeem
    Asiri, Abdullah M.
    Muddassar, Muhammad
    BIOORGANIC CHEMISTRY, 2018, 76 : 218 - 227
  • [32] Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides derived from 4-isothiocyanato-benzolamide
    Cecchi, A
    Winum, JY
    Innocenti, A
    Vullo, D
    Montero, JL
    Scozzafava, A
    Supuran, CT
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (23) : 5775 - 5780
  • [33] Carbonic anhydrase inhibitors:: Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with benzo[b]thiophene 1,1-dioxide sulfonamides
    Innocenti, A
    Villar, R
    Martinez-Merino, V
    Gll, MJ
    Scozzafava, A
    Vullo, D
    Supuran, CT
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (21) : 4872 - 4876
  • [34] Carbonic anhydrase inhibitors: Synthesis and inhibition of the human carbonic anhydrase isoforms I, II, IX and XII with benzene sulfonamides incorporating 4-and 3-nitrophthalimide moieties
    Sethi, Kalyan K.
    Verma, Saurabh M.
    Tanc, Muhammet
    Purper, Gaultier
    Calafato, Gaetan
    Carta, Fabrizio
    Supuran, Claudiu T.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (05) : 1586 - 1595
  • [35] Carbonic anhydrase inhibitors:: DNA cloning and inhibition studies of the α-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs
    Nishimori, I
    Minakuchi, T
    Morimoto, K
    Sano, S
    Onishi, S
    Takeuchi, H
    Vullo, D
    Scozzafava, A
    Supuran, CT
    JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (06) : 2117 - 2126
  • [36] 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
  • [37] Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides
    Innocenti, A
    Firnges, MA
    Antel, J
    Wurl, M
    Scozzafava, A
    Supuran, CT
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (04) : 1149 - 1154
  • [38] Recombinant human carbonic anhydrase VII: Purification, characterization, inhibition, and molecular docking studies
    Duran, Hatice Esra
    Beydemir, Sukru
    BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2023, 70 (01) : 415 - 428
  • [39] STUDIES OF RED CELL CARBONIC ANHYDRASE FOLLOWING LETHAL X-IRRADIATION
    OKUNEWIC.JP
    GLANCY, G
    HENNESSY, TG
    RADIATION RESEARCH, 1965, 25 (01) : 224 - &
  • [40] 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