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经验公式(希尔记法):
C29H34O15
化学文摘社编号:
分子量:
622.57
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352205
MDL number:
InChI key
PRVAKFUXKKVCCY-YLHHYQKRSA-N
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
assay
≥98% (HPLC)
form
powder
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
2-8°C
Quality Level
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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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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)
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)
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