InChI=1S/C27H30O15/c1- 9- 17(31) 20(34) 22(36) 26(39- 9) 38- 8- 15- 18(32) 21(35) 23(37) 27(41- 15) 42- 25- 19(33) 16- 13(30) 6- 12(29) 7- 14(16) 40- 24(25) 10- 2- 4- 11(28) 5- 3- 10/h2- 7,9,15,17- 18,20- 23,26- 32,34- 37H,8H2,1H3/t9- ,15+,17- ,18+,20+,21- ,22+,23+,26+,27- /m0/s1 |
RTATXGUCZHCSNG-QHWHWDPRSA-N |
C[C@@H] 1O[C@@H] (OC[C@H] 2O[C@@H] (Oc3c(oc4cc(O) cc(O) c4c3=O) - c3ccc(O) cc3) [C@H] (O) [C@@H] (O) [C@@H] 2O) [C@H] (O) [C@H] (O) [C@H] 1O |
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Solanum campaniforme
(IPNI:818569-1)
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Found in
leaf
(BTO:0000713).
Dried leaves were extracted with ethyl alcohol.
See:
PubMed
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radical scavenger
A role played by a substance that can react readily with, and thereby eliminate, radicals.
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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View more via ChEBI Ontology
5,7- dihydroxy- 2- (4- hydroxyphenyl)- 4- oxo- 4H- chromen- 3- yl 6- O- (6- deoxy- α- L- mannopyranosyl)- β- D- glucopyranoside
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3- ((6- O- (6- deoxy- α- L- mannopyranosyl)- β- D- glucopyranosyl)oxy)- 5,7- dihydroxy- 2- (4- hydroxyphenyl)- 4H- 1- benzopyran- 4- one
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ChemIDplus
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kaempferol 3- O- (6ʼʼ- O- α- L- rhamnopyranosyl)- β- D- glucopyranoside
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ChEBI
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Kaempferol-3-O-β-rutinoside
|
ChemIDplus
|
nicotiflorin
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ChemIDplus
|
17650-84-9
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CAS Registry Number
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ChemIDplus
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74581
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Reaxys Registry Number
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Reaxys
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21962208
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PubMed citation
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Europe PMC
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22677447
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PubMed citation
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Europe PMC
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23912804
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PubMed citation
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Europe PMC
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24123927
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PubMed citation
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Europe PMC
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24128471
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PubMed citation
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Europe PMC
|
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