The following articles (labelled with PubMed ID or TBD) are for your reviewPMID | Article Title | Published | Deposition |
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23815159 |
A class of sulfonamides with strong inhibitory action against the ?-carbonic anhydrase from Trypanosoma cruzi. |
25-JUL-2013 |
01-SEP-2020 |
28545816 |
Novel sulfonamide-containing 2-indolinones that selectively inhibit tumor-associated alpha carbonic anhydrases. |
15-JUL-2017 |
07-DEC-2019 |
23352754 |
o-Benzenedisulfonimido-sulfonamides are potent inhibitors of the tumor-associated carbonic anhydrase isoforms CA IX and CA XII. |
04-MAR-2013 |
24-SEP-2013 |
23117173 |
Microwave assisted synthesis and anti-influenza virus activity of 1-adamantyl substituted N-(1-thia-4-azaspiro[4.5]decan-4-yl)carboxamide derivatives. |
26-NOV-2012 |
17-MAY-2013 |
19435663 |
Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors. |
29-MAY-2009 |
05-DEC-2011 |
20299219 |
Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides. |
05-APR-2010 |
18-NOV-2010 |
19215141 |
Antioxidant and anticholinesterase activity evaluation of ent-kaurane diterpenoids from Sideritis arguta. |
11-MAR-2010 |
26-AUG-2010 |
19438226 |
Discovery of low nanomolar and subnanomolar inhibitors of the mycobacterial beta-carbonic anhydrases Rv1284 and Rv3273. |
02-JUL-2009 |
11-JAN-2010 |
19201197 |
Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. |
15-APR-2009 |
17-DEC-2009 |
19539481 |
Carbonic anhydrase inhibitors. Aromatic/heterocyclic sulfonamides incorporating phenacetyl, pyridylacetyl and thienylacetyl tails act as potent inhibitors of human mitochondrial isoforms VA and VB. |
15-JUL-2009 |
09-DEC-2009 |
18819811 |
Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. |
15-OCT-2008 |
05-DEC-2008 |