Found 26 hits with Last Name = 'pothen' and Initial = 'b' Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM10881
(CHEMBL288100 | MZA3 | Methazolamide | Methazolamid...)Show InChI InChI=1S/C5H8N4O3S2/c1-3(10)7-4-9(2)8-5(13-4)14(6,11)12/h1-2H3,(H2,6,11,12) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 2.10 | -49.5 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM10880
(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9) | PDB MMDB
Reactome pathway KEGG
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| 2.5 | -49.1 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM10880
(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)Show InChI InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| DrugBank MMDB PDB Article PubMed
| 12 | -45.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM10881
(CHEMBL288100 | MZA3 | Methazolamide | Methazolamid...)Show InChI InChI=1S/C5H8N4O3S2/c1-3(10)7-4-9(2)8-5(13-4)14(6,11)12/h1-2H3,(H2,6,11,12) | PDB MMDB
Reactome pathway KEGG
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| 14 | -44.8 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM50025093
(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)Show InChI InChI=1S/C6H6ClNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
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| 17.5 | -44.3 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | 3D Structure (docked) |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM10883
(4,5-dichlorobenzene-1,3-disulfonamide | CHEMBL17 |...)Show InChI InChI=1S/C6H6Cl2N2O4S2/c7-4-1-3(15(9,11)12)2-5(6(4)8)16(10,13)14/h1-2H,(H2,9,11,12)(H2,10,13,14) | PDB MMDB
Reactome pathway KEGG
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| DrugBank Article PubMed
| 26.5 | -43.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM33269
(CHEMBL277836 | azo-sulfonamide, 1d | cid_75522 | p...)Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-7-3-11(4-8-13)16-17-12-5-9-14(10-6-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 30 | -42.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM10888
(1,2-benzoxazol-3-ylmethanesulfonamide | CHEMBL750 ...)Show InChI InChI=1S/C8H8N2O3S/c9-14(11,12)5-7-6-3-1-2-4-8(6)13-10-7/h1-4H,5H2,(H2,9,11,12) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| DrugBank Article PubMed
| 35 | -42.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM10883
(4,5-dichlorobenzene-1,3-disulfonamide | CHEMBL17 |...)Show InChI InChI=1S/C6H6Cl2N2O4S2/c7-4-1-3(15(9,11)12)2-5(6(4)8)16(10,13)14/h1-2H,(H2,9,11,12)(H2,10,13,14) | PDB MMDB
Reactome pathway KEGG
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| DrugBank MMDB PDB Article PubMed
| 38 | -42.4 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM33266
(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)Show SMILES NS(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:10.10| Show InChI InChI=1S/C12H11N3O3S/c13-19(17,18)12-7-3-10(4-8-12)15-14-9-1-5-11(16)6-2-9/h1-8,16H,(H2,13,17,18) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 46 | -41.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM50025093
(4-Chloro-benzenesulfonamide | CHEMBL804 | P-Chloro...)Show InChI InChI=1S/C6H6ClNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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| Article PubMed
| 53 | -41.5 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81918
(p-Halide-sulfanilamide derivative, 2a)Show InChI InChI=1S/C6H6BrNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 68 | -40.9 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81919
(p-Halide-sulfanilamide derivative, 3)Show InChI InChI=1S/C6H6INO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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| Article PubMed
| 70 | -40.8 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81918
(p-Halide-sulfanilamide derivative, 2a)Show InChI InChI=1S/C6H6BrNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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MCE PC cid PC sid PDB UniChem
Patents
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| Article PubMed
| 81 | -40.5 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81919
(p-Halide-sulfanilamide derivative, 3)Show InChI InChI=1S/C6H6INO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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MCE PC cid PC sid UniChem
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| Article PubMed
| 81 | -40.5 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81920
(p-Hydroxy-benzene derivative, 3a)Show InChI InChI=1S/C6H7NO3S/c7-11(9,10)6-3-1-5(8)2-4-6/h1-4,8H,(H2,7,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 88 | -40.3 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81920
(p-Hydroxy-benzene derivative, 3a)Show InChI InChI=1S/C6H7NO3S/c7-11(9,10)6-3-1-5(8)2-4-6/h1-4,8H,(H2,7,9,10) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 89 | -40.2 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM10888
(1,2-benzoxazol-3-ylmethanesulfonamide | CHEMBL750 ...)Show InChI InChI=1S/C8H8N2O3S/c9-14(11,12)5-7-6-3-1-2-4-8(6)13-10-7/h1-4H,5H2,(H2,9,11,12) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| DrugBank Article PubMed
| 117 | -39.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81923
(p-Phenyldiazenyl derivative, 8)Show SMILES CNS(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:11.11| Show InChI InChI=1S/C13H13N3O3S/c1-14-20(18,19)13-8-4-11(5-9-13)16-15-10-2-6-12(17)7-3-10/h2-9,14,17H,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 277 | -37.4 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81922
(p-Phenyldiazenyl derivative, 7)Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:12.12| Show InChI InChI=1S/C14H15N3O3S/c1-17(2)21(19,20)14-9-5-12(6-10-14)16-15-11-3-7-13(18)8-4-11/h3-10,18H,1-2H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 312 | -37.1 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM33269
(CHEMBL277836 | azo-sulfonamide, 1d | cid_75522 | p...)Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-7-3-11(4-8-13)16-17-12-5-9-14(10-6-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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Patents
Similars
| Article PubMed
| 638 | -35.4 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM33266
(CHEMBL379206 | azo-sulfonamide, 1a | p-Phenyldiaze...)Show SMILES NS(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:10.10| Show InChI InChI=1S/C12H11N3O3S/c13-19(17,18)12-7-3-10(4-8-12)15-14-9-1-5-11(16)6-2-9/h1-8,16H,(H2,13,17,18) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 665 | -35.3 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81923
(p-Phenyldiazenyl derivative, 8)Show SMILES CNS(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:11.11| Show InChI InChI=1S/C13H13N3O3S/c1-14-20(18,19)13-8-4-11(5-9-13)16-15-10-2-6-12(17)7-3-10/h2-9,14,17H,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 706 | -35.1 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81922
(p-Phenyldiazenyl derivative, 7)Show SMILES CN(C)S(=O)(=O)c1ccc(cc1)N=Nc1ccc(O)cc1 |w:12.12| Show InChI InChI=1S/C14H15N3O3S/c1-17(2)21(19,20)14-9-5-12(6-10-14)16-15-11-3-7-13(18)8-4-11/h3-10,18H,1-2H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 752 | -35.0 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM81921
(p-Phenyldiazenyl derivative, 6)Show InChI InChI=1S/C15H17N3O3S/c1-18(2)22(19,20)15-10-6-13(7-11-15)17-16-12-4-8-14(21-3)9-5-12/h4-11H,1-3H3/b17-16+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 863 | -34.6 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM81921
(p-Phenyldiazenyl derivative, 6)Show InChI InChI=1S/C15H17N3O3S/c1-18(2)22(19,20)15-10-6-13(7-11-15)17-16-12-4-8-14(21-3)9-5-12/h4-11H,1-3H3/b17-16+ | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| 4.20E+3 | -30.7 | n/a | n/a | n/a | n/a | n/a | 7.4 | 25 |
Universita degli Studi di Firenze
| Assay Description Carbonic anhydrase (CA) inhibition against hCA II and V11 with synthesized compounds 2-8. |
Chem Biol Drug Des 74: 196-202 (2009)
Article DOI: 10.1111/j.1747-0285.2009.00842.x BindingDB Entry DOI: 10.7270/Q2G44NS1 |
More data for this Ligand-Target Pair | |