Sinensetin
Names | |
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IUPAC name 3′,4′,5,6,7-Pentamethoxyflavone | |
Systematic IUPAC name 2-(3,4-Dimethoxyphenyl)-5,6,7-trimethoxy-4H-1-benzopyran-4-one | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChEBI |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.230.396 |
PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C20H20O7 |
Molar mass | 372.36 g/mol |
Hazards | |
GHS labelling:[1] | |
Pictograms | |
Danger | |
Hazard statements | H301 |
Precautionary statements | P264, P270, P301+P310, P321, P330, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Sinensetin is a methylated flavone. It can be found in Orthosiphon stamineus[2] and in orange oil.[3]
References
- ^ GHS: Pubchem
- ^ Akowuah, G. A.; Ismail, Z.; Norhayati, I.; Sadikun, A. (2005). "The effects of different extraction solvents of varying polarities on polyphenols of Orthosiphon stamineus and evaluation of the free radical-scavenging activity". Food Chemistry. 93 (2): 311–317. doi:10.1016/j.foodchem.2004.09.028.
- ^ Steinke, Katrin; Jose, Elena; Sicker, Dieter; Siehl, Hans-Ullrich; Zeller, Klaus-Peter; Berger, Stefan (2013). "Sinensetin". Chemie in unserer Zeit (in German). 47 (3): 158–163. doi:10.1002/ciuz.201300627.
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Flavones and their conjugates
Monohydroxyflavone | |
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Dihydroxyflavones | |
Trihydroxyflavones | |
Tetrahydroxyflavones | |
Pentahydroxyflavones |
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O-methylated flavones |
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of apigenin | |
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of baicalein | |
of hypolaetin |
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of luteolin |
- Giraldiin A and B
- Nepitrin
- Oroxindin
- Scutellarin
Theograndin I and II
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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