|
baruol |
|
CHEBI:63712 |
|
A tetracyclic triterpenoid that is chrysene which has been fully hydrogenated except for a double bond between the 12 and 12a positions and which is substituted by methyl groups at positions 1, 1, 4b, 6a, 8 and 10a positions, and by a 4-methylpent-3-en-1-yl group at position 8 (the 2S,4aS,4bR,6aS,8R,10aR,10bS-diastereoisomer). It has been isolated from the root bark of the Panamanian tree Maytenus blepharodes. |
|
This entity has been manually annotated by the ChEBI Team.
|
|
Kristian Axelsen
|
|
|
|
Molfile
XML
SDF
|
|
|
|
InChI=1S/C30H50O/c1-21(2)10-9-15-27(5)16-19-30(8)24-13-11-22-23(12-14-25(31)26(22,3)4)29(24,7)18-17-28(30,6)20-27/h10-11,23-25,31H,9,12-20H2,1-8H3/t23-,24+,25+,27-,28+,29+,30-/m1/s1 |
XJJAVFWIAXATMT-KNUFMLCHSA-N |
[H][C@@]12CC[C@H](O)C(C)(C)C1=CC[C@@]1([H])[C@@]2(C)CC[C@@]2(C)C[C@](C)(CCC=C(C)C)CC[C@]12C |
|
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
|
|
View more via ChEBI Ontology
(2S,4aS,4bR,6aS,8R,10aR,10bS)-1,1,4b,6a,8,10a-hexamethyl-8-(4-methylpent-3-en-1-yl)-1,2,3,4,4a,4b,5,6,6a,7,8,9,10,10a,10b,11-hexadecahydrochrysen-2-ol
|
baruol
|
UniProt
|
D:B-friedobaccharan-5,21-dien-3-ol
|
ChEBI
|
9820201
|
Reaxys Registry Number
|
Reaxys
|
17705488
|
PubMed citation
|
SUBMITTER
|
|
2012-01-24
|
Needed for the reaction: (3S)-2,3-epoxy-2,3-dihydrosqualene = baruol.
|
2012-01-24
|
For original isolation, see Nunez M.J., Lopez M.R., Jimenez I.A., Moujir L.M., Ravelo A.G. and Bazzocchi I.L., Tetrahedron Lett., 2004, 45, 7367-7370.
|
|