Pectolinarin
Names
IUPAC name
5-Hydroxy-4′,6-dimethoxy-7-[α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranosyloxy]flavone
Systematic IUPAC name
(42S,43R,44S,45S,46R,72R,73R,74R,75R,76S)-25,43,44,45,73,74,75-Heptahydroxy-14,26-dimethoxy-76-methyl-24H-3,6-dioxa-2(2,7)-[1]benzopyrana-4(2,6),7(2)-bis(oxana)-1(1)-benzenaheptaphan-24H-one
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C29H34O15/c1-11-20(31)23(34)25(36)28(41-11)40-10-18-21(32)24(35)26(37)29(44-18)43-17-9-16-19(22(33)27(17)39-3)14(30)8-15(42-16)12-4-6-13(38-2)7-5-12/h4-9,11,18,20-21,23-26,28-29,31-37H,10H2,1-3H3/t11-,18+,20-,21+,23+,24-,25+,26+,28+,29+/m0/s1
    Key: DUXQKCCELUKXOE-CBBZIXHGSA-N
  • InChI=1/C29H34O15/c1-11-20(31)23(34)25(36)28(41-11)40-10-18-21(32)24(35)26(37)29(44-18)43-17-9-16-19(22(33)27(17)39-3)14(30)8-15(42-16)12-4-6-13(38-2)7-5-12/h4-9,11,18,20-21,23-26,28-29,31-37H,10H2,1-3H3/t11-,18+,20-,21+,23+,24-,25+,26+,28+,29+/m0/s1
    Key: DUXQKCCELUKXOE-CBBZIXHGBZ
  • C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O
Properties
C29H34O15
Molar mass 622.57 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Pectolinarin is a Cirsium isolate with anti-inflammatory activity and similar in chemical structure to linarin.[1]

Chemical structure of linarin
  1. ↑ Lim, H; Son, KH; Chang, HW; Bae, K; Kang, SS; Kim, HP (2008). "Anti-inflammatory activity of pectolinarigenin and pectolinarin isolated from Cirsium chanroenicum". Biological & Pharmaceutical Bulletin. 31 (11): 2063–7. doi:10.1248/bpb.31.2063. PMID 18981574.


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