Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | transcription factor Dp 1 | 0.0039 | 0.0545 | 0.0623 |
Brugia malayi | ImpB/MucB/SamB family protein | 0.0034 | 0.0383 | 0.0547 |
Mycobacterium tuberculosis | Possible DNA-damage-inducible protein P DinP (DNA polymerase V) (pol IV 2) (DNA nucleotidyltransferase (DNA-directed)) | 0.0041 | 0.0624 | 0.0399 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0031 | 0.0241 | 0.0946 |
Plasmodium falciparum | glutathione reductase | 0.0095 | 0.2551 | 1 |
Trypanosoma cruzi | trypanothione reductase, putative | 0.0095 | 0.2551 | 1 |
Leishmania major | trypanothione reductase | 0.0095 | 0.2551 | 1 |
Loa Loa (eye worm) | thioredoxin reductase | 0.0095 | 0.2551 | 0.3546 |
Mycobacterium tuberculosis | Probable membrane NADH dehydrogenase NdhA | 0.0217 | 0.691 | 0.8837 |
Loa Loa (eye worm) | ImpB/MucB/SamB family protein | 0.0034 | 0.0383 | 0.022 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Brugia malayi | Pre-SET motif family protein | 0.0212 | 0.6758 | 1 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0031 | 0.0241 | 0.0946 |
Leishmania major | protein kinase, putative,polo-like protein kinase, putative | 0.0093 | 0.2492 | 0.9735 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Mycobacterium ulcerans | DNA polymerase IV | 0.0062 | 0.1355 | 1 |
Mycobacterium tuberculosis | Probable oxidoreductase | 0.0241 | 0.7776 | 1 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Brugia malayi | dihydrolipoyl dehydrogenase, mitochondrial precursor, putative | 0.0033 | 0.0328 | 0.0464 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Schistosoma mansoni | hypothetical protein | 0.0167 | 0.5147 | 0.5028 |
Loa Loa (eye worm) | Pin1-type peptidyl-prolyl cis-trans isomerase | 0.0034 | 0.037 | 0.0199 |
Giardia lamblia | DINP protein human, muc B family | 0.0041 | 0.0624 | 0.1372 |
Schistosoma mansoni | tyrosyl-DNA phosphodiesterase | 0.0067 | 0.1562 | 0.1355 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Mycobacterium leprae | DIHYDROLIPOAMIDE DEHYDROGENASE LPD (LIPOAMIDE REDUCTASE (NADH)) (LIPOYL DEHYDROGENASE) (DIHYDROLIPOYL DEHYDROGENASE) (DIAPHORASE | 0.0241 | 0.7776 | 1 |
Trypanosoma brucei | dihydrolipoamide dehydrogenase | 0.0033 | 0.0328 | 0.1284 |
Echinococcus granulosus | dna polymerase kappa | 0.0062 | 0.1355 | 0.2336 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0034 | 0.037 | 0.0056 |
Echinococcus multilocularis | geminin | 0.0167 | 0.5147 | 1 |
Plasmodium vivax | thioredoxin reductase, putative | 0.0095 | 0.2551 | 1 |
Mycobacterium tuberculosis | Dihydrolipoamide dehydrogenase LpdC (lipoamide reductase (NADH)) (lipoyl dehydrogenase) (dihydrolipoyl dehydrogenase) (diaphoras | 0.0241 | 0.7776 | 1 |
Trypanosoma brucei | trypanothione reductase | 0.0095 | 0.2551 | 1 |
Brugia malayi | serine/threonine-protein kinase plk-2 | 0.0093 | 0.2492 | 0.3674 |
Mycobacterium tuberculosis | Probable NADH dehydrogenase Ndh | 0.0217 | 0.691 | 0.8837 |
Entamoeba histolytica | deoxycytidyl transferase, putative | 0.0034 | 0.0383 | 0.0197 |
Trypanosoma cruzi | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.4623 |
Trypanosoma brucei | tyrosyl-DNA Phosphodiesterase (Tdp1), putative | 0.0067 | 0.1562 | 0.6123 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Echinococcus granulosus | tyrosyl DNA phosphodiesterase 1 | 0.0067 | 0.1562 | 0.2754 |
Trypanosoma brucei | peptidyl-prolyl cis-trans isomerase/rotamase, putative | 0.0033 | 0.0341 | 0.1336 |
Trypanosoma brucei | dihydrolipoyl dehydrogenase | 0.0033 | 0.0328 | 0.1284 |
Schistosoma mansoni | rotamase | 0.0034 | 0.037 | 0.0133 |
Echinococcus multilocularis | dihydrolipoamide dehydrogenase | 0.0033 | 0.0328 | 0.0179 |
Wolbachia endosymbiont of Brugia malayi | dihydrolipoamide dehydrogenase E3 component | 0.0033 | 0.0328 | 0.5 |
Brugia malayi | Thioredoxin reductase | 0.0095 | 0.2551 | 0.3762 |
Echinococcus granulosus | terminal deoxycytidyl transferase rev1 | 0.0034 | 0.0383 | 0.0371 |
Echinococcus granulosus | expressed protein | 0.0034 | 0.037 | 0.0344 |
Trypanosoma cruzi | peptidyl-prolyl cis-trans isomerase | 0.0033 | 0.0341 | 0.006 |
Schistosoma mansoni | dihydrolipoamide dehydrogenase | 0.0033 | 0.0328 | 0.009 |
Toxoplasma gondii | peptidylprolyl isomerase | 0.0033 | 0.0341 | 0.0437 |
Plasmodium vivax | dihydrolipoyl dehydrogenase, mitochondrial, putative | 0.0033 | 0.0328 | 0.0379 |
Brugia malayi | Tyrosyl-DNA phosphodiesterase family protein | 0.0067 | 0.1562 | 0.2295 |
Trichomonas vaginalis | DNA polymerase eta, putative | 0.0062 | 0.1355 | 0.1374 |
Leishmania major | tyrosyl-DNA phosphodiesterase 1 | 0.0067 | 0.1562 | 0.5552 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Trypanosoma brucei | unspecified product | 0.0055 | 0.1114 | 0.4368 |
Loa Loa (eye worm) | glutathione reductase | 0.0095 | 0.2551 | 0.3546 |
Brugia malayi | polk-prov protein | 0.0038 | 0.0504 | 0.0726 |
Trypanosoma brucei | DNA polymerase eta, putative | 0.0034 | 0.0383 | 0.1502 |
Echinococcus multilocularis | thioredoxin glutathione reductase | 0.0095 | 0.2551 | 0.471 |
Trypanosoma brucei | dihydrolipoamide dehydrogenase, point mutation | 0.0033 | 0.0328 | 0.1284 |
Echinococcus multilocularis | expressed protein | 0.0034 | 0.037 | 0.0264 |
Echinococcus multilocularis | terminal deoxycytidyl transferase rev1 | 0.0034 | 0.0383 | 0.0292 |
Trypanosoma brucei | polo-like protein kinase | 0.0093 | 0.2492 | 0.9769 |
Schistosoma mansoni | terminal deoxycytidyl transferase | 0.0034 | 0.0383 | 0.0147 |
Treponema pallidum | NADH oxidase | 0.0033 | 0.0328 | 0.5 |
Mycobacterium tuberculosis | Conserved hypothetical protein | 0.0034 | 0.0383 | 0.0075 |
Brugia malayi | Pin1-type peptidyl-prolyl cis-trans isomerase, BmPin1 | 0.0034 | 0.037 | 0.0527 |
Trichomonas vaginalis | set domain proteins, putative | 0.0242 | 0.7809 | 1 |
Entamoeba histolytica | serine/threonine protein kinase, putative | 0.0093 | 0.2492 | 1 |
Brugia malayi | hypothetical protein | 0.0149 | 0.4498 | 0.6648 |
Mycobacterium tuberculosis | NADPH-dependent mycothiol reductase Mtr | 0.0095 | 0.2551 | 0.2985 |
Toxoplasma gondii | NADPH-glutathione reductase | 0.0033 | 0.0328 | 0.0379 |
Giardia lamblia | Kinase, PLK | 0.0093 | 0.2492 | 1 |
Schistosoma mansoni | DNA polymerase eta | 0.0034 | 0.0383 | 0.0147 |
Echinococcus multilocularis | dna polymerase eta | 0.0034 | 0.0383 | 0.0292 |
Onchocerca volvulus | 0.0149 | 0.4498 | 0.5625 | |
Wolbachia endosymbiont of Brugia malayi | dihydrolipoamide dehydrogenase E3 component | 0.0033 | 0.0328 | 0.5 |
Echinococcus multilocularis | serine:threonine protein kinase PLK1 | 0.0093 | 0.2492 | 0.459 |
Trypanosoma cruzi | peptidyl-prolyl cis-trans isomerase | 0.0033 | 0.0341 | 0.006 |
Mycobacterium ulcerans | DNA polymerase IV | 0.0062 | 0.1355 | 1 |
Toxoplasma gondii | pyruvate dehydrogenase complex subunit PDH-E3II | 0.0033 | 0.0328 | 0.0379 |
Schistosoma mansoni | hypothetical protein | 0.0167 | 0.5147 | 0.5028 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0038 | 0.0504 | 0.1975 |
Echinococcus granulosus | geminin | 0.0167 | 0.5147 | 1 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0046 | 0.0804 | 0.0636 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Loa Loa (eye worm) | hypothetical protein | 0.0149 | 0.4498 | 0.6532 |
Mycobacterium tuberculosis | Probable reductase | 0.0217 | 0.691 | 0.8837 |
Entamoeba histolytica | tyrosyl-DNA phosphodiesterase, putative | 0.0067 | 0.1562 | 0.5676 |
Onchocerca volvulus | 0.0242 | 0.7809 | 1 | |
Trichomonas vaginalis | CAMK family protein kinase | 0.0046 | 0.0804 | 0.0636 |
Loa Loa (eye worm) | PLK/PLK1 protein kinase | 0.0093 | 0.2492 | 0.3456 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0031 | 0.0241 | 0.0946 |
Leishmania major | DNA polymerase eta, putative | 0.0034 | 0.0383 | 0.025 |
Toxoplasma gondii | thioredoxin reductase | 0.0095 | 0.2551 | 1 |
Trypanosoma cruzi | DNA polymerase eta, putative | 0.0034 | 0.0383 | 0.025 |
Trypanosoma cruzi | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.4623 |
Loa Loa (eye worm) | pre-SET domain-containing protein family protein | 0.0212 | 0.6758 | 1 |
Plasmodium vivax | dihydrolipoyl dehydrogenase, apicoplast, putative | 0.0033 | 0.0328 | 0.0379 |
Trichomonas vaginalis | DNA polymerase IV / kappa, putative | 0.0062 | 0.1355 | 0.1374 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Trypanosoma cruzi | tyrosyl-DNA Phosphodiesterase (Tdp1), putative | 0.0067 | 0.1562 | 0.5552 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Mycobacterium tuberculosis | Putative ferredoxin reductase | 0.0217 | 0.691 | 0.8837 |
Echinococcus granulosus | thioredoxin glutathione reductase | 0.0095 | 0.2551 | 0.4753 |
Brugia malayi | glutathione reductase | 0.0095 | 0.2551 | 0.3762 |
Trypanosoma cruzi | polo-like protein kinase, putative | 0.0093 | 0.2492 | 0.9735 |
Trypanosoma cruzi | polo-like protein kinase, putative | 0.0093 | 0.2492 | 0.9735 |
Schistosoma mansoni | rab geranylgeranyl transferase alpha subunit | 0.0034 | 0.0383 | 0.0147 |
Brugia malayi | ImpB/MucB/SamB family protein | 0.0034 | 0.0383 | 0.0547 |
Echinococcus granulosus | histone lysine methyltransferase setb | 0.003 | 0.024 | 0.0081 |
Plasmodium falciparum | thioredoxin reductase | 0.0095 | 0.2551 | 1 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0041 | 0.0624 | 0.2448 |
Mycobacterium tuberculosis | Probable dehydrogenase | 0.0217 | 0.691 | 0.8837 |
Onchocerca volvulus | Serine\/threonine kinase homolog | 0.0093 | 0.2492 | 0.2976 |
Chlamydia trachomatis | dihydrolipoyl dehydrogenase | 0.0033 | 0.0328 | 0.5 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Echinococcus multilocularis | dna polymerase kappa | 0.0062 | 0.1355 | 0.2274 |
Echinococcus granulosus | transcription factor Dp 1 | 0.0039 | 0.0545 | 0.0699 |
Trypanosoma brucei | DNA polymerase IV, putative | 0.0062 | 0.1355 | 0.5313 |
Trypanosoma cruzi | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.4623 |
Echinococcus granulosus | serine:threonine protein kinase PLK1 | 0.0093 | 0.2492 | 0.4634 |
Loa Loa (eye worm) | tyrosyl-DNA phosphodiesterase | 0.0067 | 0.1562 | 0.2028 |
Leishmania major | DNA polymerase kappa, putative | 0.0041 | 0.0624 | 0.1335 |
Schistosoma mansoni | kinase | 0.0047 | 0.0848 | 0.0623 |
Mycobacterium tuberculosis | Probable nitrite reductase [NAD(P)H] large subunit [FAD flavoprotein] NirB | 0.0217 | 0.691 | 0.8837 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Mycobacterium tuberculosis | NAD(P)H quinone reductase LpdA | 0.0241 | 0.7776 | 1 |
Trypanosoma brucei | DNA polymerase IV, putative | 0.0062 | 0.1355 | 0.5313 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0093 | 0.2492 | 0.2308 |
Trichomonas vaginalis | rotamase, putative | 0.0033 | 0.0341 | 0.0018 |
Trypanosoma brucei | dihydrolipoamide dehydrogenase | 0.0033 | 0.0328 | 0.1284 |
Plasmodium vivax | glutathione reductase, putative | 0.0095 | 0.2551 | 1 |
Leishmania major | DNA polymerase kappa, putative,DNA polymerase IV, putative | 0.0041 | 0.0624 | 0.1335 |
Trypanosoma cruzi | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.4623 |
Loa Loa (eye worm) | hypothetical protein | 0.0038 | 0.0504 | 0.0405 |
Brugia malayi | Pre-SET motif family protein | 0.003 | 0.024 | 0.0334 |
Echinococcus multilocularis | tyrosyl DNA phosphodiesterase 1 | 0.0067 | 0.1562 | 0.2694 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0093 | 0.2492 | 0.2893 |
Loa Loa (eye worm) | hypothetical protein | 0.0034 | 0.0383 | 0.022 |
Trichomonas vaginalis | rotamase, putative | 0.0034 | 0.037 | 0.0056 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0062 | 0.1355 | 0.5313 |
Trypanosoma brucei | DNA polymerase kappa, putative | 0.0038 | 0.0504 | 0.1975 |
Echinococcus granulosus | dihydrolipoamide dehydrogenase | 0.0033 | 0.0328 | 0.0258 |
Leishmania major | peptidyl-prolyl cis-trans isomerase/rotamase, putative,PPIase, putative | 0.0033 | 0.0341 | 0.006 |
Echinococcus granulosus | dna polymerase eta | 0.0034 | 0.0383 | 0.0371 |
Trypanosoma brucei | DNA polymerase IV, putative | 0.0055 | 0.1114 | 0.4368 |
Trypanosoma cruzi | tyrosyl-DNA Phosphodiesterase (Tdp1), putative | 0.0067 | 0.1562 | 0.5552 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 0.5 h after the drug administered with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 hr with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 h after the drug administered with dose of 100 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 100 mg/kg; 0/3= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 0.5 h with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 0.5 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 0.5 h with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 4 hr with dose of 30 mg/kg; 0/2= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 0.5 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 h after the drug administered with dose of 100 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 0.5 h after the drug administered with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 0.5 h with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 hr with dose of 300 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | - 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 15 min in rats; - means No protection | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | - 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 30 min in rats; -means No protection | ChEMBL. | 15294003 |
Activity (functional) | - 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 1 hr in rats; -means No protection | ChEMBL. | 15294003 |
Activity (functional) | 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 2 hr in rats; + means 25% of the animals protected | ChEMBL. | 15294003 |
Activity (functional) | - 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 4 hr in rats; -means No protection | ChEMBL. | 15294003 |
Activity (functional) | - 0 | Toxicity of the compound after oral administration of 100 mg/kg dose in rats; + means 25% of the animals were protected | ChEMBL. | 15294003 |
Activity (functional) | 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 30 min in rats; +++ means 75% of the animals protected | ChEMBL. | 15294003 |
Activity (functional) | 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 1 hr in rats; + means 25% of the animals protected | ChEMBL. | 15294003 |
Activity (functional) | 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 4 hr in rats; +means 25% of the animals protected | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 0.5 h with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for subcutaneous metrazol test at 4 h after the drug administered with dose of 30 mg/kg; 0/1= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 4 hr with dose of 30 mg/kg; 0/2= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Activity (functional) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse at maximal electroshock test at 4 h after the drug administered with dose of 100 mg/kg; 0/3= No of animals protected /No of animals tested | ChEMBL. | 15294003 |
Anticonvulsant Activity (functional) | - 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 15 min in rats; - means No protection | ChEMBL. | 15294003 |
Anticonvulsant Activity (functional) | 0 | Anticonvulsant activity of the compound after oral administration of 100 mg/kg dose after 2 hr in rats;++ means 50% of the animals protected | ChEMBL. | 15294003 |
clogP | = 0.88 | Calculated partition coefficient (clogP) | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 0.5 h with dose of 100 mg/kg; 0/8= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 4 hr with dose of 100 mg/kg; 0/4= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 0.5 h with dose of 300 mg/kg; 0/4= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 4 hr with dose of 300 mg/kg; 0/2= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Toxicity (ADMET) | - 0 | Toxicity of the compound after oral administration of 100 mg/kg dose in rats; - means No toxicity | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 0.5 h with dose of 30 mg/kg; 0/4= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Toxicity (ADMET) | = 0 | Anti convulsant activity of the compound administered intra peritoneally to mouse for toxicity at 4 hr with dose of 30 mg/kg; 0/2= No of animals exhibiting toxicity /No of animals tested | ChEMBL. | 15294003 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.