Nishimori Isao, Vullo Daniela, Minakuchi Tomoko, Morimoto Kaori, Onishi Saburo, Scozzafava Andrea, Supuran Claudiu T
Department of Gastroenterology and Hepatology, Kochi Medical School, Nankoku, Kochi 783-8505, Japan.
Bioorg Med Chem Lett. 2006 Apr 15;16(8):2182-8. doi: 10.1016/j.bmcl.2006.01.044. Epub 2006 Feb 3.
A library of sulfonamides/sulfamates has been investigated for the inhibition of the carboxyterminal truncated form of the alpha-carbonic anhydrase (CA, EC 4.2.1.1) isolated from the gastric pathogen Helicobacter pylori (hpCA). This enzyme, incorporating 202 amino acid residues, showed a catalytic activity similar to that of the full length hpCA, with k(cat) of 2.35 x 10(5)s(-1) and k(cat)/K(M) of 1.56 x 10(7)M(-1)s(-1) at 25 degrees C and pH of 8.9, for the CO(2) hydration reaction. All types of activity for inhibition of the bacterial enzyme have been detected. Dorzolamide and simple 4-substituted benzenesulfonamides were weak hpCA inhibitors (inhibition constants, K(I)s, in the range of 830-4310 nM). Sulfanilamide, orthanilamide, some of their derivatives, and indisulam showed better activity (K(I)s in the range of 310-562 nM), whereas most of the clinically used CA inhibitors, such as methazolamide, ethoxzolamide, dichlorophenamide, brinzolamide, topiramate, zonisamide, etc., acted as medium potency hpCA inhibitors (K(I)s in the range of 124-287 nM). Some potent hpCA inhibitors were detected too (K(I)s in the range of 20-96 nM) such as acetazolamide, 4-amino-6-chloro-1,3-benzenedisulfonamide, 4-sulfanilyl-aminoethyl-benzenesulfonamide, and 4-(2-amino-pyrimidin-4-yl)-benzenesulfonamide. Most of the investigated derivatives acted as better inhibitors of the human isoform hCA II than as hpCA inhibitors. Since hpCA is essential for the survival of the pathogen in acid, its inhibition by compounds such as those investigated here might be used as a new pharmacologic tool in the management of drug resistant H. pylori.
已对一系列磺胺类/氨基磺酸盐进行了研究,以考察其对从胃病原体幽门螺杆菌(hpCA)中分离出的α-碳酸酐酶(CA,EC 4.2.1.1)的羧基末端截短形式的抑制作用。这种含有202个氨基酸残基的酶,在25℃和pH 8.9条件下,对于CO₂水合反应,其催化活性与全长hpCA相似,催化常数k(cat)为2.35×10⁵ s⁻¹,催化效率k(cat)/K(M)为1.56×10⁷ M⁻¹ s⁻¹。已检测到所有类型的对该细菌酶的抑制活性。多佐胺和简单的4-取代苯磺酰胺是较弱的hpCA抑制剂(抑制常数K(I)在830 - 4310 nM范围内)。磺胺、邻磺胺、它们的一些衍生物以及茚地那韦表现出较好的活性(K(I)在310 - 562 nM范围内),而大多数临床使用的CA抑制剂,如甲醋唑胺、乙氧唑胺、二氯苯酰胺、布林佐胺、托吡酯、唑尼沙胺等,是中等效力的hpCA抑制剂(K(I)在124 - 287 nM范围内)。还检测到一些强效的hpCA抑制剂(K(I)在20 - 96 nM范围内),如乙酰唑胺、4-氨基-6-氯-1,3-苯二磺酰胺、4-磺胺基氨基乙基苯磺酰胺和4-(2-氨基嘧啶-4-基)苯磺酰胺。大多数研究的衍生物对人同工型hCA II的抑制作用比对hpCA的抑制作用更好。由于hpCA对于病原体在酸性环境中的存活至关重要,因此本文所研究的这类化合物对其的抑制作用可能用作治疗耐药幽门螺杆菌的一种新的药理学工具。