Psilozina
| Psilozina | |
|---|---|
 | |
| Formula kimikoa | C12H16N2O |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Konposizioa | Nitrogeno, karbono, hidrogeno eta oxigeno |
| Mota | tryptamine alkaloid (en)  |
| Masa molekularra | 204,126 Da |
| Erabilera | |
| Rola | haluzinogeno eta enteogeno |
| Identifikatzaileak | |
| InChlKey | SPCIYGNTAMCTRO-UHFFFAOYSA-N |
| CAS zenbakia | 520-53-6 |
| ChemSpider | 4807 |
| PubChem | 4980 |
| Reaxys | 160503 |
| Gmelin | 8613 |
| ChEMBL | CHEMBL65547 |
| EC zenbakia | 208-296-5 |
| ECHA | 100.007.543 |
| MeSH | C009105 |
| Human Metabolome Database | HMDB0042000 |
| KNApSAcK | C00001427 |
| UNII | CMS88KUW0G |
| KEGG | C08312 |
| PDB Ligand | 91Q |
Psilozina (4-hidroxi-N,N-dimetiltriptamina) psilozibinatik eratorritako alkaloide bat da, onddo haluzinogeno gehienetan dagoena. Propietate enteogenoak ditu. Uste da O-azetilpsilozina psilozina-profarmakoa dela.[1]
Albert Hofmann kimikari suitzarrak, Hans Tscherter laborategiko teknikariarekin batera, psilozina eta psilozibina isolatu zituen lehen aldiz Sandoz laborategietan, onddo haluzinogenoetatik abiatuta, 1959an.
Erreferentziak
- ↑ (Ingelesez) Bauer, Barbara E.. (2019-09-18). «The State of the Art of Psilacetin (4-AcO-DMT)» Psychedelic Science Review.
Kanpo estekak
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Artikulu hau kimikari buruzko zirriborroa da. Wikipedia lagun dezakezu edukia osatuz. |
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