From Wikipedia, the free encyclopedia
Plicatin A
Names
Preferred IUPAC name
Methyl (2E )-3-{4-hydroxy-3-[(2R )-2-hydroxy-3-methylbut-3-en-1-yl]phenyl}prop-2-enoate
Identifiers
131889-82-2 Y
3D model (JSmol )
InChI=1S/C15H18O4/c1-10(2)14(17)9-12-8-11(4-6-13(12)16)5-7-15(18)19-3/h4-8,14,16-17H,1,9H2,2-3H3/b7-5+/t14-/m1/s1
Key: ROCPNNHDHKREAV-HZRUHFOJSA-N
CC(=C)[C@@H](CC1=C(C=CC(=C1)/C=C/C(=O)OC)O)O
Properties
C 15 H 18 O 4
Molar mass
262.305 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y (what is Y N ?)
Infobox references
Chemical compound
Plicatin A is a hydroxycinnamic acid found in Psoralea plicata .[1]
References [ ]
^ Rasool, Nazli; Khan, Abdul Qasim; Malik, Abdul (1990). "Plicatin a and B, two phenolic cinnamates from Psoralea plicata". Phytochemistry . 29 (12): 3979–3981. doi :10.1016/0031-9422(90)85385-S .
Aglycones
Precursor Monohydroxycinnamic acids (Coumaric acids) Dihydroxycinnamic acids Trihydroxycinnamic acids O -methylated formsothers
Esters
glycoside-likes
Esters of caffeic acid with cyclitols
Glycosides
Tartaric acid estersOther esters with caffeic acid Caffeoyl phenylethanoid glycoside (CPG)
Echinacoside
, , ,
, ,
, , , , , , ,
Verbascoside (, )
Oligomeric forms
Conjugates withcoenzyme A (CoA)
Categories :
Hydroxycinnamic acid esters Vinylogous carboxylic acids Aromatic compound stubs Hidden categories:
Articles without InChI source Chemical pages without ChemSpiderID Articles without EBI source Articles without KEGG source Articles without UNII source Chembox CAS registry number not linked Pages using collapsible list with both background and text-align in titlestyle Articles containing unverified chemical infoboxes Chembox image size set Articles with short description Short description matches Wikidata All stub articles