Revision as of 16:52, 16 July 2021 editJJMC89 bot III (talk | contribs)Bots, Administrators3,684,692 editsm Moving Category:Heterocyclic compounds (2 rings) to Category:Heterocyclic compounds with 2 rings per Misplaced Pages:Categories for discussion/Log/2021 June 24#Category:Heterocyclic compounds (1 ring)← Previous edit | Latest revision as of 16:09, 18 August 2022 edit undoFswitzer4 (talk | contribs)Extended confirmed users10,572 editsm Added UNII | ||
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| CASNo_Ref = {{cascite|changed|ChemSpider}} | | CASNo_Ref = {{cascite|changed|ChemSpider}} | ||
| CASNo = 369376-61-4 | | CASNo = 369376-61-4 | ||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = A69767WW45 | |||
| ChEMBL_Ref = {{ebicite|correct|EBI}} | | ChEMBL_Ref = {{ebicite|correct|EBI}} | ||
| ChEMBL = 450490 | | ChEMBL = 450490 |
Latest revision as of 16:09, 18 August 2022
Names | |
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Preferred IUPAC name 1-ethan-1-one | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEMBL | |
ChemSpider | |
PubChem CID | |
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Properties | |
Chemical formula | C13H11ClO2 |
Molar mass | 234.678 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Pterulone is a fungal metabolite. It was initially isolated from the mycelium and liquid cultures of wood-decay fungus in the genus Pterula. The compound inhibits eukaryotic respiration by targeting the mitochondrial NADH:ubiquinone oxidoreductase.
References
- Engler M, Anke T, Sterner O, Brandt U (1997). "Pterulinic acid and pterulone, two novel inhibitors of NADH:ubiquinone oxidoreductase (complex I) produced by a Pterula species. I. Production, isolation and biological activities". Journal of Antibiotics. 50 (4): 325–9. doi:10.7164/antibiotics.50.325. PMID 9186558.
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