Kamazuleno
| Kamazuleno | |
|---|---|
 | |
| Formula kimikoa | C14H16 |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Mota | konposatu kimiko |
| Masa molekularra | 184,125 Da |
| Identifikatzaileak | |
| InChlKey | GXGJIOMUZAGVEH-UHFFFAOYSA-N |
| CAS zenbakia | 529-05-5 |
| ChemSpider | 10268 |
| PubChem | 10719 |
| Gmelin | 3573 |
| ChEMBL | CHEMBL495665 |
| EC zenbakia | 208-449-6 |
| ECHA | 100.007.682 |
| CosIng | 32631 |
| Human Metabolome Database | HMDB0036470 |
| KNApSAcK | C00003114 |
| UNII | Z439UH6E5F |
| KEGG | C09633 |
Kamazulenoa edo 7-etil-1,4-dimetilazulenoa konposatu organikoa C14H16, formula duena, seskiterpenoen klasekoa. Azulenoaren deribatu ordezkatua da. Fusio-puntu baxuko (25 C) solido urdina da. Hainbat landare-olioen osagaia da, kamamilarena edo asentsioarena esaterako[1].
Kamazulenoa ezaugarri antiinflamatorioak eta antioxidatzaileak ditu.
Sintesia
Kamazulenoa matrizinatik abiatuz biosintetizatzen da[2].
Erreferentziak
- ↑ (Ingelesez) PubChem. «Chamazulene» pubchem.ncbi.nlm.nih.gov (kontsulta data: 2024-09-24).
- ↑ (Ingelesez) Safayhi, H.; Sabieraj, J.; Sailer, E.-R.; Ammon, H. P. T.. (1994-10). «Chamazulene: An Antioxidant-Type Inhibitor of Leukotriene B4 Formation» Planta Medica 60 (05): 410–413. doi:. ISSN 0032-0943. (kontsulta data: 2024-09-24).
Kanpo estekak
| Autoritate kontrola |
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|---|
Datuak: Q909088
Multimedia: Chamazulene / Q909088
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Index:
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