albendazole-2-aminosulfone: a major metabolite of albendazole; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
| ID Source | ID |
|---|---|
| PubMed CID | 88125 |
| CHEBI ID | 80621 |
| SCHEMBL ID | 761154 |
| SCHEMBL ID | 23392493 |
| MeSH ID | M0227890 |
| Synonym |
|---|
| albendazole-2-aminosulfone |
| 80983-34-2 |
| abz2nh2 |
| 2-amino-5-n-propylsulfonylbenzimidazole |
| 6-propylsulfonyl-1h-benzimidazol-2-amine |
| 2-amino-5-propylsulphonylbenzimidazole |
| 9rj4tyc7eb , |
| 5-(propylsulfonyl)-1h-benzimidazol-2-amine |
| 1h-benzimidazol-2-amine, 5-(propylsulfonyl)- |
| (2-amino-5-propylsulfonyl)benzimidazole |
| unii-9rj4tyc7eb |
| AKOS024318936 |
| 2-amino-5-n-propylsulphonylbenzimidazole |
| amino albendazole sulfone |
| 6-(propylsulfonyl)-1h-benzimidazol-2-amine |
| FT-0611188 |
| CHEBI:80621 |
| DTXSID80230823 |
| SCHEMBL761154 |
| 2-aminoalbendazole sulfone |
| WTPBIYSMFKUQKY-UHFFFAOYSA-N |
| 5-(propylsulfonyl)-1h-benzo[d]imidazol-2-amine |
| mfcd01075656 |
| albendazole-2-aminosulfone, analytical standard |
| 2-amino-5-n-propylsulfonylbenzimidazole, aldrichcpr |
| 5-propylsulfonyl-1h-benzimidazole-2-amine |
| 5-(propane-1-sulfonyl)-1h-1,3-benzodiazol-2-amine |
| AS-63856 |
| 5-(propylsulphonyl) -1h-benzimidazol-2-amine |
| Q27149669 |
| albendazole-2-aminosulfone 100 microg/ml in acetonitrile |
| E79073 |
| 5-(propylsulphonyl)-1h-benzimidazol-2-amine |
| 6-(propylsulfonyl)-1h-benzimidazol-2-amine albendazole-2-aminosulfone |
| 2-amino-5-1h-propylsulfonylbenzimidazole |
| skf-81038 |
| albendazole-2-amino sulfone |
| albendazole impurity d [ep impurity] |
| (2-amino-1h-benzimidazol-5-yl)propyl-.lambda.6-sulfanedione |
| 5-(propylsulfonyl)-1h-benzo(d)imidazol-2-amine |
| A899977 |
| SCHEMBL23392493 |
| CS-W012818 |
| Excerpt | Relevance | Reference |
|---|---|---|
| " The procedure was applied to the determination of albendazole and its 3 metabolites in the muscle tissue of the 2 fish species after orally dosing them with albendazole." | ( Determination of albendazole and its metabolites in the muscle tissue of hybrid striped and largemouth bass using liquid chromatography with fluorescence detection. Rummel, N; Shaikh, B, ) | 0.13 |
| Class | Description |
|---|---|
| organic sulfide | Compounds having the structure RSR (R =/= H). Such compounds were once called thioethers. |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] | |
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.72) All Compounds (24.57) |
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 6 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||