首页> 外文OA文献 >Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors

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Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors

机译：N-（5-甲基 - 异恶唑-3-基/ 1,3,4-噻唑-2-基）-4-（3-取代除苯基脲酰基）苯磺酰胺作为人碳酸酐酶同工酶I，II，II，II， VII和XII抑制剂

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Chandra Bhushan Mishra; Shikha Kumari; Andrea Angeli; Simona Maria Monti; Martina Buonanno; Amresh Prakash; Manisha Tiwari; Claudiu T. Supuran;
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1. Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors [J] . Mishra Chandra Bhushan, Kumari Shikha, Angeli Andrea, Journal of enzyme inhibition and medicinal chemistry. . 2016,第Suppla2期

机译：N-（5-甲基 - 异恶唑-3-基/ 1,3,4-噻唑-2-基）-4-（3-取代除苯基脲酰基）苯磺酰磺酰胺作为人碳酸酐酶Iso酶I，II，II，II， VII和XII抑制剂
2. Design, synthesis and biological evaluation of N -(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors [J] . Chandra Bhushan Mishra, Shikha Kumari, Andrea Angeli, Journal of enzyme inhibition and medicinal chemistry. . 2016,第Suppa2期

机译：N-（5-甲基-异恶唑-3-基/ 1,3,4-噻二唑-2-基）-4-（3-取代的苯基脲基）苯磺酰胺作为人碳酸酐酶同工酶I，II的设计，合成和生物学评价VII和XII抑制剂
3. Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: structure-based drug design, synthesis, and biological evaluation. [J] . Vernier W, Chong W, Rewolinski D, Bioorganic and medicinal chemistry . 2010,第9期

机译：碳酸酐酶II和IV的硫醚苯磺酰胺抑制剂：基于结构的药物设计，合成和生物学评估。
4. Design, Synthesis, and Biological Evaluation of Nedd4 E3 Ubiquitin Ligase Small Molecule Inhibitors [C] . Xiaoli Fu, Jie Chu, Yuyin Li, International conference on applied biotechnology . 2014

机译：Nedd4 E3泛素连接酶小分子抑制剂的设计，合成和生物学评估
5. Design and synthesis of molecular probes to modulate cell membrane permeation: I. Design, synthesis, and biological evaluation of novel chicoric acid analogues as inhibitors of HIV-1 integrase. II. Design, synthesis, and biological evaluation of novel estradiol analogues targeting the membrane estrogen receptor. [D] . Charvat, Trevor Thomas. 2004

机译：设计和合成的分子探针，可调节细胞膜的渗透性：I.设计，合成和生物评价作为抗HIV-1整合酶抑制剂的新型菊苣酸类似物。二。针对膜雌激素受体的新型雌二醇类似物的设计，合成和生物学评估。
6. Intrinsic Thermodynamics and Structure Correlation of Benzenesulfonamides with a Pyrimidine Moiety Binding to Carbonic Anhydrases I II VII XII and XIII [O] . Miglė Kišonaitė, Asta Zubrienė, Edita Čapkauskaitė, -1

机译：与碳酸酐酶IIIVIIXII和XIII结合的嘧啶部分的苯磺酰胺的内在热力学和结构相关性
7. Carbonic anhydrase inhibitors: guaiacol and catechol derivatives effectively inhibit certain human carbonic anhydrase isoenzymes (hCA I, II, IX and XII) [O] . Andrea Scozzafava, Maurizio Passaponti, Claudiu T. Supuran, 2014

机译：碳酸酐酶抑制剂：Guaiacol和儿茶酚衍生物有效抑制某些人碳酸酐酶同工酶（HCA I，II，IX和XII）

Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors

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