| Identification | Back Directory | [Name]
Quercetin 3-O-rutinoside-(1→2)-O-rhamnoside | [CAS]
55696-57-6 | [Synonyms]
Manghaslin
Quercetin-3-O-(2-α-L-rhamnosyl)-rutinoside
Quercetin 3-O-rutinoside-(1→2)-O-rhamnoside
Quercetin 3-O-rhamnosyl(1→2)[rhamnosyl-[(1→6)]glucoside
Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside
4H-1-Benzopyran-4-one, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[6-deoxy-α-L-mannopyranosyl-(1→6)]-β-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy- | [Molecular Formula]
C33H40O20 | [MOL File]
55696-57-6.mol | [Molecular Weight]
756.66 |
| Chemical Properties | Back Directory | [Melting point ]
168-170 °C(Solv: ethyl acetate (141-78-6); methanol (67-56-1)) | [Boiling point ]
1090.4±65.0 °C(Predicted) | [density ]
1.79±0.1 g/cm3(Predicted) | [form ]
Solid | [pka]
6.17±0.40(Predicted) | [color ]
Light yellow to yellow |
| Hazard Information | Back Directory | [Uses]
Manghaslin is a flavonoid glycoside with anti-inflammatory activities. Manghaslin shows inhibitory activity against AChE with an IC50 of 94.92 μM[1][2]. | [Definition]
ChEBI: Manghaslin is a glycoside and a member of flavonoids. | [IC 50]
AChE | [References]
[1] Hasan K?rm?z?bekmez, et al. Phenolic compounds from the aerial parts of Clematis viticella L. and their in vitro anti-inflammatory activities. Nat Prod Res. 2019 Sep;33(17):2541-2544. DOI:10.1080/14786419.2018.1448815
[2] Daniil N Olennikov, et al. Isorhamnetin and Quercetin Derivatives as Anti-Acetylcholinesterase Principles of Marigold (Calendula officinalis) Flowers and Preparations. Int J Mol Sci. 2017 Aug 2;18(8):1685. DOI:10.3390/ijms18081685 |
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