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(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol |
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CHEBI:67643 |
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(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol |
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A flavonolignan isolated from the stems of Sinocalamus affinis. |
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This entity has been manually annotated by the ChEBI Team.
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Molfile
XML
SDF
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InChI=1S/C27H26O11/c1-34-20-6-13(4-5-16(20)30)26(33)24(12-28)38-27-22(35-2)7-14(8-23(27)36-3)19-11-18(32)25-17(31)9-15(29)10-21(25)37-19/h4-11,24,26,28-31,33H,12H2,1-3H3/t24-,26-/m0/s1 |
WXNJNHFYIWEHIL-AHWVRZQESA-N |
COc1cc(ccc1O)[C@H](O)[C@H](CO)Oc1c(OC)cc(cc1OC)-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',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
has role
plant metabolite
(CHEBI:76924)
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
is a
dimethoxybenzene
(CHEBI:51681)
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
is a
flavonolignan
(CHEBI:72709)
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
is a
polyphenol
(CHEBI:26195)
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
is a
primary alcohol
(CHEBI:15734)
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
(CHEBI:67643)
is a
secondary alcohol
(CHEBI:35681)
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2-(4-{[(1S,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy}-3,5-dimethoxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
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tricin 4'-O-(threo-β-guaiacylglyceryl) ether
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ChEBI
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21559783
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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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