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SMB00344

Sigma-Aldrich

Pectolinarin

≥98% (HPLC)

Synonym(s):

Pectolinarin, 7-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one, Pectolinaroside, 5,7-Dihydroxy 4′,6-dimethoxyflavone 7-rutinoside, Pectolinarigenin 7-rutinoside

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About This Item

Empirical Formula (Hill Notation):
C29H34O15
CAS Number:
28978-02-1
Molecular Weight:
622.57
MDL number:
MFCD12546128
UNSPSC Code:
12352205
PubChem Substance ID:
329824964
NACRES:
NA.25
Pricing and availability is not currently available.

Quality Level

200

assay

≥98% (HPLC)

form

powder

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

2-8°C

SMILES string

OC1=C(C(C=C(C2=CC=C(C=C2)OC)O3)=O)C3=CC(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@H]5[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O5)O4)=C1OC

InChI

1S/C30H36O14/c1-12-22(32)26(36)28(38)30(42-12)41-11-14-8-19(24(34)27(37)23(14)33)44-20-10-18-21(25(35)29(20)40-3)16(31)9-17(43-18)13-4-6-15(39-2)7-5-13/h4-7,9-10,12,14,19,22-24,26-28,30,32-38H,8,11H2,1-3H3/t12-,14+,19+,22-,23+,24-,26+,27-,28+,30+/m0/s1

InChI key

PRVAKFUXKKVCCY-YLHHYQKRSA-N

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General description

Pectolinarinis a glycosylated flavonoid that is generally found in several Cirsium spp. and was first extracted from Linaria vulgaris. The chemical structure has a rutinoside conjugate of pectolinarigenin at the 7-O position.

Biochem/physiol Actions

Pectolinarinexerts anti-inflammatory, antioxidant, antidiabetic, and antitumor activities. It is known to be a potent agent for the treatment of neurodegenerative disorders. It also displays antiviral, and antiparasitic effects and can inhibit bacterial biofilm formation. Pectolinarin relieves lipopolysaccharide-induced liver and kidney injuries.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000344478
SLCN0597
SLCG5783
SLCG2022
SLBQ8427V

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P-EP017. Biological potential and neuroprotective activity of pectolinarin in the management of neurodegenerative disorders: Phytotherapeutic importance through data analysis of various scientific works
Patel Dinesh Kumar and Patel Kanika
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, 132(8), e83-e84 (2021)
Purification Process and In Vitro and In Vivo Bioactivity Evaluation of Pectolinarin and Linarin from Cirsium japonicum
Ye Yana, et al.,
Molecules (Basel), 27 (24), 8695-8695 (2022)

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