Homotaurina
| Homotaurina | |
|---|---|
| Formula kimikoa | C3H9NO3S |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Mota | konposatu kimiko |
| Masa molekularra | 139,03 Da |
| Erabilera | |
| Rola | antiepileptiko eta GABA agonist (en) |
| Identifikatzaileak | |
| InChlKey | SNKZJIOFVMKAOJ-UHFFFAOYSA-N |
| CAS zenbakia | 3687-18-1 |
| ChemSpider | 1584 |
| PubChem | 1646 eta 6991996 |
| Gmelin | 1457 eta 194495 |
| ChEMBL | CHEMBL149082 |
| EC zenbakia | 222-977-4 |
| ECHA | 100.020.889 |
| CosIng | 31513 |
| MeSH | C001355 |
| RxNorm | 1374845 |
| Human Metabolome Database | HMDB0253211 |
| UNII | 5K8EAX0G53 |
| KEGG | D06202 eta C03349 |
| PDB Ligand | A20 |
Homotaurina edo azido 3-aminopropanosulfonikoa konposatu organikoa da C3H9NO3S formula duena azido sulfonikoen klasekoa. Solidoa da. Narritagarria da[1].
Homotaurina produktu naturala da eta algen metabolitoa da. Akanprosatoa sintetizatzeko lehengai gisa baliatzen da[2].
Erreferentziak
- ↑ (Ingelesez) PubChem. «Tramiprosate» pubchem.ncbi.nlm.nih.gov (kontsulta data: 2025-10-04).
- ↑ Lednicer, Daniel. (2007). The Organic Chemistry of Drug Synthesis. (1st ed. argitaraldia) John Wiley & Sons, Incorporated ISBN 978-0-470-18066-2. (kontsulta data: 2025-10-04).
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