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 |
|---|
| - 28978-02-1
Y
|
| |
| ChEMBL | |
| ChemSpider | |
| |
| UNII | - BY44L9O1RR
Y
|
| |
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 |
|---|
| CHO |
| 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 linarinExternal links
- ^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.