InChI=1S/C30H44O5/c1- 18- 23(33) 19(32) 15- 21- 27(4) 12- 14- 29(6) 22- 16- 26(3,24(34) 35) 10- 9- 25(22,2) 11- 13- 28(29,5) 20(27) 7- 8- 30(18,21) 17- 31/h17,20- 22,33H,7- 16H2,1- 6H3,(H,34,35) /t20- ,21- ,22+,25+,26+,27+,28+,29- ,30- /m0/s1 |
CDOKUYLTAYCBST-XBBQATOGSA-N |
O=C[C@@] 12[C@] ([C@] 3([C@@] ([C@@] 4([C@@] (CC3) ([C@@] 5(C[C@@] (CC[C@@] 5(CC4) C) (C(O) =O) C) [H] ) C) C) (CC1) [H] ) C) (CC(=O) C(O) =C2C) [H]![](images/invisible_space.gif) |
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Tripterygium wilfordii
(NCBI:txid458696)
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Found in
bark
(BTO:0001301).
See:
PubMed
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Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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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
(2R,4aS,6aR,6bS,8aR,12aS,12bR,14aS,14bR)- 8a- formyl- 10- hydroxy- 2,4a,6a,9,12b,14a- hexamethyl- 11- oxo- 1,2,3,4,4a,5,6,6a,6b,7,8,8a,11,12,12a,12b,13,14,14a,14b- icosahydropicene- 2- carboxylic acid
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138884-84-1
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CAS Registry Number
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KNApSAcK
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4891672
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Reaxys Registry Number
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Reaxys
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10993235
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PubMed citation
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Europe PMC
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18996177
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PubMed citation
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Europe PMC
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338605
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Chinese Abstracts citation
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Europe PMC
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