| Assay ID | Title | Year | Journal | Article |
|---|
| AID366657 | Inhibition of human cloned CA1 by CO2 hydration assay | 2008 | Bioorganic & medicinal chemistry letters, Aug-15, Volume: 18, Issue:16
| Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives. |
| AID306207 | Antimicrobial activity against Staphylococcus aureus | 2007 | Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
| Anti-mycobacterial activity of a bis-sulfonamide. |
| AID353230 | Inhibition of human recombinant CA9 by stopped flow CO2 hydration assay | 2009 | Bioorganic & medicinal chemistry letters, Apr-15, Volume: 19, Issue:8
| Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties. |
| AID306206 | Antimicrobial activity against Escherichia coli | 2007 | Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
| Anti-mycobacterial activity of a bis-sulfonamide. |
| AID306208 | Antimicrobial activity against Vibrio harveyi | 2007 | Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
| Anti-mycobacterial activity of a bis-sulfonamide. |
| AID281086 | Selectivity ratio of human CA9 over human CA2 | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| AID353228 | Inhibition of human recombinant CA1 by stopped flow CO2 hydration assay | 2009 | Bioorganic & medicinal chemistry letters, Apr-15, Volume: 19, Issue:8
| Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties. |
| AID353231 | Inhibition of human recombinant CA12 by stopped flow CO2 hydration assay | 2009 | Bioorganic & medicinal chemistry letters, Apr-15, Volume: 19, Issue:8
| Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties. |
| AID366659 | Inhibition of human recombinant CA5A by CO2 hydration assay | 2008 | Bioorganic & medicinal chemistry letters, Aug-15, Volume: 18, Issue:16
| Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives. |
| AID281084 | Inhibition of catalytic domain of human recombinant isozyme CA9 by CO2 hydration method | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| AID281083 | Inhibition of human recombinant isozyme CA2 by CO2 hydration method | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| AID300870 | Selectivity ratio of Ki for human cloned CA1 to Ki for human cloned catalytic domain CA9 | 2007 | Bioorganic & medicinal chemistry letters, Sep-15, Volume: 17, Issue:18
| Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety. |
| AID281082 | Inhibition of human recombinant isozyme CA1 by CO2 hydration method | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| AID366660 | Inhibition of human recombinant CA5B by CO2 hydration assay | 2008 | Bioorganic & medicinal chemistry letters, Aug-15, Volume: 18, Issue:16
| Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives. |
| AID300868 | Inhibition of human cloned CA2 by CO2 hydration method | 2007 | Bioorganic & medicinal chemistry letters, Sep-15, Volume: 17, Issue:18
| Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety. |
| AID300867 | Inhibition of human cloned CA1 by CO2 hydration method | 2007 | Bioorganic & medicinal chemistry letters, Sep-15, Volume: 17, Issue:18
| Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety. |
| AID353229 | Inhibition of human recombinant CA2 by stopped flow CO2 hydration assay | 2009 | Bioorganic & medicinal chemistry letters, Apr-15, Volume: 19, Issue:8
| Inhibition of carbonic anhydrase isozymes with benzene sulfonamides incorporating thio, sulfinyl and sulfonyl glycoside moieties. |
| AID306204 | Antimicrobial activity against Mycobacterium smegmatis | 2007 | Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
| Anti-mycobacterial activity of a bis-sulfonamide. |
| AID300869 | Inhibition of human cloned catalytic domain CA9 by CO2 hydration method | 2007 | Bioorganic & medicinal chemistry letters, Sep-15, Volume: 17, Issue:18
| Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety. |
| AID300871 | Selectivity ratio of Ki for human cloned CA1 to Ki for human cloned catalytic domain CA9 | 2007 | Bioorganic & medicinal chemistry letters, Sep-15, Volume: 17, Issue:18
| Inhibition of carbonic anhydrase isozymes I, II and IX with benzenesulfonamides containing an organometallic moiety. |
| AID306205 | Antimicrobial activity against Candida albicans | 2007 | Bioorganic & medicinal chemistry letters, Mar-01, Volume: 17, Issue:5
| Anti-mycobacterial activity of a bis-sulfonamide. |
| AID366658 | Inhibition of human cloned CA2 by CO2 hydration assay | 2008 | Bioorganic & medicinal chemistry letters, Aug-15, Volume: 18, Issue:16
| Inhibition of human mitochondrial carbonic anhydrases VA and VB with para-(4-phenyltriazole-1-yl)-benzenesulfonamide derivatives. |
| AID281085 | Selectivity ratio of human CA9 over human CA1 | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| AID1797360 | CA Inhibition Assay from Article 10.1021/jm061320h: \\Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides.\\ | 2007 | Journal of medicinal chemistry, Apr-05, Volume: 50, Issue:7
| Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |