Plicatin A

Plicatin A
Chemical structure of 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
CAS Number
  • 131889-82-2 checkY
3D model (JSmol)
  • Interactive image
PubChem CID
  • 15730631
CompTox Dashboard (EPA)
  • DTXSID101127557 Edit this at Wikidata
InChI
  • 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
Chemical formula
C15H18O4
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).
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Infobox references
Chemical compound

Plicatin A is a hydroxycinnamic acid found in Psoralea plicata.[1]

References

  1. ^ Rasool, Nazli; Khan, Abdul Qasim; Malik, Abdul (1990). "Plicatin a and B, two phenolic cinnamates from Psoralea plicata". Phytochemistry. 29 (12): 3979–3981. Bibcode:1990PChem..29.3979R. doi:10.1016/0031-9422(90)85385-S.
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Types of hydroxycinnamic acids
Aglycones
Precursor
  • Cinnamic acid
Monohydroxycinnamic acids
(Coumaric acids)
  • p-Coumaric acid
  • o-Coumaric acid
  • m-Coumaric acid
Dihydroxycinnamic acids
  • Caffeic acid (3,4-dihydroxycinnamic acid)
  • Umbellic acid (2,4-dihydroxycinnamic acid)
  • 2,3-Dihydroxycinnamic acid
  • 2,5-Dihydroxycinnamic acid
  • 3,5-Dihydroxycinnamic acid
Trihydroxycinnamic acids
O-methylated forms
others
Esters
glycoside-likes
Esters of
caffeic acid
with cyclitols
esters of
quinic acid
  • Chlorogenic acid (3-caffeoylquinic acid)
  • Cryptochlorogenic acid (4-O-caffeoylquinic acid)
  • Neochlorogenic acid (5-O-Caffeoylquinic acid)
  • Cynarine (1,5-dicaffeoylquinic acid)
  • 3,4-dicaffeoylquinic acid
  • 3,5-dicaffeoylquinic acid
esters of
shikimic acid
Glycosides
  • Ferulic acid glucoside
  • p-Coumaric acid glucoside
  • 1-Sinapoyl-D-glucose
Tartaric acid esters
Other esters
with caffeic acid
Caffeoyl phenylethanoid
glycoside (CPG)
  • Echinacoside
  • Calceolarioside A, B, C, F
  • Chiritoside A, B, C
  • Cistanoside A, B, C, D, E, F, G, H
  • Conandroside
  • Myconoside
  • Pauoifloside
  • Plantainoside A
  • Plantamajoside
  • Tubuloside B
  • Verbascoside (Isoverbascoside, 2′-Acetylverbascoside)
Oligomeric forms
Dimers
Trimers
Tetramers
  • Tetraferulic acids
Conjugates with
coenzyme A (CoA)


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