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(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol |
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CHEBI:67641 |
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(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',5'-dimethoxy-4',8''-oxyflavonolignan-7'',9''-diol |
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A flavonolignan isolated from the stems of Sinocalamus affinis. |
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![](images/goldenstar.gif) ![](images/goldenstar.gif)
This entity has been manually annotated by the ChEBI Team.
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Molfile
XML
SDF
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InChI=1S/C26H24O10/c1- 33- 21- 7- 14(19- 11- 18(31) 24- 17(30) 9- 16(29) 10- 20(24) 35- 19) 8- 22(34- 2) 26(21) 36- 23(12- 27) 25(32) 13- 3- 5- 15(28) 6- 4- 13/h3- 11,23,25,27- 30,32H,12H2,1- 2H3/t23- ,25- /m0/s1 |
XWGDMVNWFZRSNF-ZCYQVOJMSA-N |
COc1cc(cc(OC)c1O[C@@H](CO)[C@@H](O)c1ccc(O)cc1)-c1cc(=O)c2c(O)cc(O)cc2o1 |
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Sinocalamus affinis
(IPNI:421970-1)
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Found in
stem
(BTO:0001300).
95% Ethanolic extract of skin-removed, air-dried, powdered stems.
See:
PubMed
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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
Outgoing
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(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
has role
plant metabolite
(CHEBI:76924)
(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
is a
dimethoxybenzene
(CHEBI:51681)
(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
is a
flavonolignan
(CHEBI:72709)
(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
is a
polyphenol
(CHEBI:26195)
(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
is a
primary alcohol
(CHEBI:15734)
(−)- (7''S,8''S)- 4'',5,7- trihydroxy- 3',5'- dimethoxy- 4',8''- oxyflavonolignan- 7'',9''- diol
(CHEBI:67641)
is a
secondary alcohol
(CHEBI:35681)
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2- (4- {[(1S,2S)- 1,3- dihydroxy- 1- (4- hydroxyphenyl)propan- 2- yl]oxy}- 3,5- dimethoxyphenyl)- 5,7- dihydroxy- 4H- chromen- 4- one
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21559779
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Reaxys Registry Number
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Reaxys
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21469695
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PubMed citation
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Europe PMC
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