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8 similar compounds to monomer 87064

Compile data set for download or QSAR
Wt: 554.7
BDBM50114172
Wt: 538.7
BDBM87061
Purchase
Wt: 554.7
BDBM87062
Purchase
Wt: 570.7
BDBM87063
Wt: 554.7
BDBM50114178
Wt: 538.7
BDBM50114118
Wt: 570.7
BDBM50114230
Wt: 554.7
BDBM50114167

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 18 hits for monomerid = 50114172,87061,87062,87063,50114178,50114118,50114230,50114167   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50114178
PNG
((R)-4-((5S,6R,8S,9R,10S,11S,14S,17R)-3,7,12-Trihyd...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20+,22+,25+,26-/m1/s1
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0.900n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50114118
PNG
((1R,2R)-4-((8S,9S,12R,14R,17S)-3-(R)-Hydroxy-10,13...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O4S2/c1-15(4-9-22(32)28-23-29-30-24(35-23)36(27,33)34)19-7-8-20-18-6-5-16-14-17(31)10-12-25(16,2)21(18)11-13-26(19,20)3/h15-21,31H,4-14H2,1-3H3,(H2,27,33,34)(H,28,29,32)/t15-,16-,17-,18+,19-,20+,21+,25+,26-/m1/s1
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10n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Carbonic Anhydrase IV


(Bos taurus (bovine))
BDBM50114178
PNG
((R)-4-((5S,6R,8S,9R,10S,11S,14S,17R)-3,7,12-Trihyd...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20+,22+,25+,26-/m1/s1
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16n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), obtained from bovine lung microsomes


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic Anhydrase IV


(Bos taurus (bovine))
BDBM50114118
PNG
((1R,2R)-4-((8S,9S,12R,14R,17S)-3-(R)-Hydroxy-10,13...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O4S2/c1-15(4-9-22(32)28-23-29-30-24(35-23)36(27,33)34)19-7-8-20-18-6-5-16-14-17(31)10-12-25(16,2)21(18)11-13-26(19,20)3/h15-21,31H,4-14H2,1-3H3,(H2,27,33,34)(H,28,29,32)/t15-,16-,17-,18+,19-,20+,21+,25+,26-/m1/s1
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28n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), obtained from bovine lung microsomes


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50114178
PNG
((R)-4-((5S,6R,8S,9R,10S,11S,14S,17R)-3,7,12-Trihyd...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20+,22+,25+,26-/m1/s1
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48n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50114230
PNG
((R)-4-((5S,6R,8S,9S,12S,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O6S2/c1-13(4-7-21(34)28-23-29-30-24(37-23)38(27,35)36)16-5-6-17-22-18(12-20(33)26(16,17)3)25(2)9-8-15(31)10-14(25)11-19(22)32/h13-20,22,31-33H,4-12H2,1-3H3,(H2,27,35,36)(H,28,29,34)/t13-,14+,15-,16-,17+,18+,19-,20+,22+,25+,26-/m1/s1
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50n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50114167
PNG
((R)-4-((8S,10S,12S,14R,15R,17S)-3,12-Di(R)-hydroxy...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-9-22(33)28-23-29-30-24(36-23)37(27,34)35)18-7-8-19-17-6-5-15-12-16(31)10-11-25(15,2)20(17)13-21(32)26(18,19)3/h14-21,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15-,16-,17+,18-,19+,20+,21+,25+,26-/m1/s1
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50n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50114172
PNG
((R)-4-((5S,6R,8S,9S,12R,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20-,22+,25+,26-/m1/s1
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52n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase II (CA2)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic Anhydrase IV


(Bos taurus (bovine))
BDBM50114167
PNG
((R)-4-((8S,10S,12S,14R,15R,17S)-3,12-Di(R)-hydroxy...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-9-22(33)28-23-29-30-24(36-23)37(27,34)35)18-7-8-19-17-6-5-15-12-16(31)10-11-25(15,2)20(17)13-21(32)26(18,19)3/h14-21,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15-,16-,17+,18-,19+,20+,21+,25+,26-/m1/s1
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130n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), obtained from bovine lung microsomes


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50114167
PNG
((R)-4-((8S,10S,12S,14R,15R,17S)-3,12-Di(R)-hydroxy...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-9-22(33)28-23-29-30-24(36-23)37(27,34)35)18-7-8-19-17-6-5-15-12-16(31)10-11-25(15,2)20(17)13-21(32)26(18,19)3/h14-21,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15-,16-,17+,18-,19+,20+,21+,25+,26-/m1/s1
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200n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic Anhydrase IV


(Bos taurus (bovine))
BDBM50114230
PNG
((R)-4-((5S,6R,8S,9S,12S,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O6S2/c1-13(4-7-21(34)28-23-29-30-24(37-23)38(27,35)36)16-5-6-17-22-18(12-20(33)26(16,17)3)25(2)9-8-15(31)10-14(25)11-19(22)32/h13-20,22,31-33H,4-12H2,1-3H3,(H2,27,35,36)(H,28,29,34)/t13-,14+,15-,16-,17+,18+,19-,20+,22+,25+,26-/m1/s1
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205n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), obtained from bovine lung microsomes


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50114118
PNG
((1R,2R)-4-((8S,9S,12R,14R,17S)-3-(R)-Hydroxy-10,13...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O4S2/c1-15(4-9-22(32)28-23-29-30-24(35-23)36(27,33)34)19-7-8-20-18-6-5-16-14-17(31)10-12-25(16,2)21(18)11-13-26(19,20)3/h15-21,31H,4-14H2,1-3H3,(H2,27,33,34)(H,28,29,32)/t15-,16-,17-,18+,19-,20+,21+,25+,26-/m1/s1
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210n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic Anhydrase IV


(Bos taurus (bovine))
BDBM50114172
PNG
((R)-4-((5S,6R,8S,9S,12R,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20-,22+,25+,26-/m1/s1
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240n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine carbonic anhydrase IV (CA4), obtained from bovine lung microsomes


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50114172
PNG
((R)-4-((5S,6R,8S,9S,12R,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)/t14-,15+,16-,17-,18+,19+,20-,22+,25+,26-/m1/s1
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410n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50114230
PNG
((R)-4-((5S,6R,8S,9S,12S,14R,17S)-7-Hydroxy-3-(R)-h...)
Show SMILES C[C@H](CCC(=O)Nc1nnc(s1)S(N)(=O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C
Show InChI InChI=1S/C26H42N4O6S2/c1-13(4-7-21(34)28-23-29-30-24(37-23)38(27,35)36)16-5-6-17-22-18(12-20(33)26(16,17)3)25(2)9-8-15(31)10-14(25)11-19(22)32/h13-20,22,31-33H,4-12H2,1-3H3,(H2,27,35,36)(H,28,29,34)/t13-,14+,15-,16-,17+,18+,19-,20+,22+,25+,26-/m1/s1
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420n/an/an/an/an/an/an/an/a



Universit£ degli Studi di Firenze

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant carbonic anhydrase I (CA1)


Bioorg Med Chem Lett 12: 1551-7 (2002)


Article DOI: 10.1016/s0960-894x(02)00252-4
BindingDB Entry DOI: 10.7270/Q2B56K7W
More data for this
Ligand-Target Pair
Glutathione oxidoreductase (GR)


(Escherichia coli)
BDBM87062
PNG
(Sulfonamide derivative, 2)
Show SMILES CC(CCC(=O)Nc1nnc(s1)S(N)(=O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CCC12C
Show InChI InChI=1S/C26H42N4O5S2/c1-14(4-7-21(33)28-23-29-30-24(36-23)37(27,34)35)17-5-6-18-22-19(9-11-26(17,18)3)25(2)10-8-16(31)12-15(25)13-20(22)32/h14-20,22,31-32H,4-13H2,1-3H3,(H2,27,34,35)(H,28,29,33)
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6.10E+3n/a 4.50E+3n/an/an/an/an/an/a



Dumlupinar University



Assay Description
The enzyme activities in the absence of drugs or chemicals were taken as 100%. For each drug or chemical, an activity%-(drug) graph was drawn and dr...


J Enzyme Inhib Med Chem 23: 418-23 (2008)


Article DOI: 10.1080/14756360701546413
BindingDB Entry DOI: 10.7270/Q2F18XBP
More data for this
Ligand-Target Pair
Glutathione oxidoreductase (GR)


(Escherichia coli)
BDBM87061
PNG
(Sulfonamide derivative, 1)
Show SMILES CC(CCC(=O)Nc1nnc(s1)S(N)(=O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Show InChI InChI=1S/C26H42N4O4S2/c1-15(4-9-22(32)28-23-29-30-24(35-23)36(27,33)34)19-7-8-20-18-6-5-16-14-17(31)10-12-25(16,2)21(18)11-13-26(19,20)3/h15-21,31H,4-14H2,1-3H3,(H2,27,33,34)(H,28,29,32)
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7.23E+4n/a 4.71E+4n/an/an/an/an/an/a



Dumlupinar University



Assay Description
The enzyme activities in the absence of drugs or chemicals were taken as 100%. For each drug or chemical, an activity%-(drug) graph was drawn and dr...


J Enzyme Inhib Med Chem 23: 418-23 (2008)


Article DOI: 10.1080/14756360701546413
BindingDB Entry DOI: 10.7270/Q2F18XBP
More data for this
Ligand-Target Pair
6-phosphogluconate dehydrogenase (6PGD)


(Homo sapiens (Human))
BDBM87063
PNG
(Sulfonamide derivative, 3)
Show SMILES CC(CCC(=O)Nc1nnc(s1)S(N)(=O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C
Show InChI InChI=1S/C26H42N4O6S2/c1-13(4-7-21(34)28-23-29-30-24(37-23)38(27,35)36)16-5-6-17-22-18(12-20(33)26(16,17)3)25(2)9-8-15(31)10-14(25)11-19(22)32/h13-20,22,31-33H,4-12H2,1-3H3,(H2,27,35,36)(H,28,29,34)
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8.78E+4n/a 6.01E+4n/an/an/an/an/an/a



Dumlupinar University



Assay Description
The enzyme activities in the absence of drugs or chemicals were taken as 100%. For each drug or chemical, an activity%-(drug) graph was drawn and dr...


J Enzyme Inhib Med Chem 23: 418-23 (2008)


Article DOI: 10.1080/14756360701546413
BindingDB Entry DOI: 10.7270/Q2F18XBP
More data for this
Ligand-Target Pair