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Carbonic anhydrase inhibitors. V: Pyrylium salts in the synthesis of isozyme-specific inhibitors.
1992 C. T. Supuran;G. Manole;A. Dinculescu;A. Schiketanz;M. D. Gheorghiu;I. Puscas;A. T. Balaban
Carbonic anhydrase activators. VII. Isozyme II activation by bisazolyl-methanes, -ethanes and related azoles.
1993 C. T. Supuran;A. T. Balaban;P. Cabildo;R. M. Claramunt;J. L. Lavandera;J. Elguero
Carbonic anhydrase inhibitors. Part 11. Coordination compounds of heterocyclic sulfonamides with lanthanides are potent inhibitors of isozymes I and II.
1993 C. T. Supuran;G. Manole;M. Andruh
Carbonic anhydrase activators. 3: structure-activity correlations for a series of isozyme II activators.
1994 B. W. Clare;C. T. Supuran
Thienothiopyransulfonamides as complexing agents for the preparation of dual carbonic anhydrase inhibitors.
1995 C. T. Supuran
Metal Complexes of 1,3,4-Thiadiazole-2,5-Disulfonamide are Strong Dual Carbonic Anhydrase Inhibitors, although the Ligand Possesses very Weak such Properties.
1995 C. T. Supuran
Complexes With Biologically Active Ligands. Part 6 Ni(II) Coordination Compounds of Hydrazine and Heterocyclic Sulfonamides as Inhibitors of the Zinc Enzyme Carbonic Anhydrase.
1996 J. Borràs;J. Casanova;T. Cristea;A. Gheorghe;A. Scozzafava;C. T. Supuran;V. Tudor
Complexes With Biologically Active Ligands. Part 2. Preparation of Copper(II) Complexes of Positively-Charged Derivatives of Aminoglutethimide.
1996 C. T. Supuran
1,3,4-thiadiazole derivatives. Part 9. Synthesis and biological activity of metal complexes of 5-(2-aminoethyl)-2-amino-1,3,4-thiadiazole.
1996 M. Barboiu;M. Cimpoesu;C. Guran;C. T. Supuran
Complexes with biologically active ligands. Part 4. Coordination compounds of chlorothiazide with transition metal ions behave as strong carbonic anhydrase inhibitors.
1996 C. T. Supuran
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Tipologia
- 1 - Contributo su rivista 1898
- 1 - Contributo su rivista::1a - Articolo su rivista 1898
- 2 - Contributo in volume 13
- 2 - Contributo in volume::2a - Art/Cap/Saggio libro scient/tech 12
- 6 - Brevetti e copyright 7
- 6 - Brevetti e copyright::6a - Brevetto attivo 7
- 2 - Contributo in volume::2c - Prefazione/postfazione 1
- 3 - Libro 1
- 3 - Libro::3f - Libro scientifico/tecnico 1
Data di pubblicazione
- 2020 - 2024 466
- 2010 - 2019 970
- 2000 - 2009 432
- 1992 - 1999 51
Editore
- Elsevier 6
- Springer 3
- Academic Press Inc. 1
- American Chemical Society:1155 Sixteenth Street Northwest:Washington, DC 20036:(800)227-5558, EMAIL: service@acs.org, INTERNET: http://www.pubs.acs.org, Fax: (614)447-3671 1
- Bentham 1
- CRC Press 1
- Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598 Editore precedente:Prof Ugo Croatto Luogo pubbl. Padova Ultimo luogo pubblicazione: Lausanne. 1
- Future Medicine Ltd. 1
- John Libby Eurotext Ltd:127 avenue de la Republique, F 92120 Montrouge France:011 33 1 46730660, EMAIL: marketing@jle.com, INTERNET: http://www.john-libbey-eurotext.fr, Fax: 011 33 1 40840999 1
- John Wiley & Sons, Inc. 1
Rivista
- JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 399
- BIOORGANIC & MEDICINAL CHEMISTRY 197
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 180
- JOURNAL OF MEDICINAL CHEMISTRY 128
- EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 91
- BIOORGANIC CHEMISTRY 82
- BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS 37
- EXPERT OPINION ON THERAPEUTIC PATENTS 37
- MOLECULES 35
- JOURNAL OF ENZYME INHIBITION 34
Serie
- TOPICS IN MEDICINAL CHEMISTRY 3
Keyword
- Humans 636
- Carbonic Anhydrase Inhibitors 631
- Carbonic Anhydrases 552
- Carbonic anhydrase 406
- Sulfonamides 402
- Structure-Activity Relationship 397
- Drug Discovery3003 Pharmaceutical Science 292
- Molecular Structure 266
- Isoenzymes 254
- Animals 216
Lingua
- eng 1411
- enm 1
- ita 1
Accesso al fulltext
- no fulltext 1635
- open 154
- reserved 119
- partially open 9
- embargoed 2