:Pectolinarin

{{Chembox

| ImageFile = Pectolinarin.svg

| ImageSize = 250px

| ImageAlt =

| IUPACName = 5-Hydroxy-4′,6-dimethoxy-7-[α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranosyloxy]flavone

| SystematicName = (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

| OtherNames =

|Section1={{Chembox Identifiers

| CASNo = 28978-02-1

| CASNo_Ref = {{cascite|correct|CAS}}

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = BY44L9O1RR

| PubChem = 168849

| ChEMBL = 445978

| ChemSpiderID = 147700

| 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

| InChIKey = DUXQKCCELUKXOE-CBBZIXHGBZ

| StdInChI = 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

| StdInChIKey = DUXQKCCELUKXOE-CBBZIXHGSA-N

| SMILES = 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}}

|Section2={{Chembox Properties

| Formula = C₂₉H₃₄O₁₅

| MolarMass = 622.57 g/mol

| Appearance =

| Density =

| MeltingPt =

| BoilingPt =

| Solubility = }}

|Section3={{Chembox Hazards

| MainHazards =

| FlashPt =

| AutoignitionPt = }}

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Pectolinarin is a Cirsium isolate with anti-inflammatory activity and similar in chemical structure to linarin.{{cite journal|pmid=18981574|year=2008|last1=Lim|first1=H|last2=Son|first2=KH|last3=Chang|first3=HW|last4=Bae|first4=K|last5=Kang|first5=SS|last6=Kim|first6=HP|title=Anti-inflammatory activity of pectolinarigenin and pectolinarin isolated from Cirsium chanroenicum|volume=31|issue=11|pages=2063–7|journal=Biological & Pharmaceutical Bulletin|doi=10.1248/bpb.31.2063|url=https://www.jstage.jst.go.jp/article/bpb/31/11/31_11_2063/_pdf|doi-access=free}}

File:linarin.svg]]{{clear left}}