InChI=1S/C30H48O4/c1- 18- 23(32) 19(31) 16- 21- 27(18,4) 9- 8- 20- 28(21,5) 13- 15- 30(7) 22- 17- 26(3,24(33) 34) 11- 10- 25(22,2) 12- 14- 29(20,30) 6/h18- 22,31H,8- 17H2,1- 7H3,(H,33,34) /t18- ,19+,20- ,21+,22+,25+,26+,27+,28+,29+,30- /m0/s1 |
KVLFXTHBJNNYDP-KWDXJSKJSA-N |
[C@@] 12(CC[C@] 3([C@] (C[C@H] (C([C@@H] 3C) =O) O) ([H] ) [C@@] 1(CC[C@@] 4([C@@] 2(CC[C@@] 5([C@] 4(C[C@@] (CC5) (C(O) =O) C) [H] ) C) C) C) C) C) [H]![](images/invisible_space.gif) |
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Tripterygium doianum
(NCBI:txid859951)
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See:
Phytochem., 61, (2002), 93
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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,8aS,9R,11R,12aS,12bS,14aS,14bR)- 11- hydroxy- 2,4a,6a,8a,9,12b,14a- heptamethyl- 10- oxodocosahydropicene- 2- carboxylic acid
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158629-70-0
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CAS Registry Number
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KNApSAcK
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7779868
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Reaxys Registry Number
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Reaxys
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