RhamnocitrinRhamnocitrin - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-N1353-01.804-HY-N1353-01804-HY-N1353-01Business & Industrial > Science & LaboratoryRhamnocitrin
Gentaur
EUR12027-02-22

Rhamnocitrin

CAT:
804-HY-N1353-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Rhamnocitrin - image 1

Rhamnocitrin

  • Description:

    Rhamnocitrin is an anti-inflammatory and antioxidant agent that targets STIM-1, NFATc3 and MAPK pathways and can scavenge DPPH (IC50=28.38 mM) . Rhamnocitrin selectively inhibits oxidative stress and inflammatory responses in vascular endothelial cells and neurons. Rhamnocitrin up-regulates miR-185 to inhibit STIM-1-mediated store-operated calcium entry (SOCE), thereby blocking NFATc3 nuclear translocation and downstream inflammatory factor expression, while inducing heme oxygenase HO-1 expression and regulating the ERK/p38 MAPK pathway, inhibiting antioxidant and pro-inflammatory cytokines (such as IL-6, IL-8) and adhesion molecules (such as ICAM-1, VCAM-1) . Rhamnocitrin can be used in the study of endothelial-related inflammatory diseases (such as sepsis, acute lung injury, atherosclerosis) and neuroprotection (such as oxidative damage of PC12 cells) [1][2][3][4].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    P38 MAPK
  • Type:

    Natural Products
  • Related Pathways:

    MAPK/ERK Pathway
  • Applications:

    COVID-19-immunoregulation
  • Field of Research:

    Inflammation/Immunology; Cardiovascular Disease
  • Assay Protocol:

    https://www.medchemexpress.com/rhamnocitrin.html
  • Purity:

    99.67
  • Solubility:

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles:

    O=C1C(O)=C(C2=CC=C(O)C=C2)OC3=CC(OC)=CC(O)=C13
  • Molecular Formula:

    C16H12O6
  • Molecular Weight:

    300.26
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Li Y, et al. Simultaneous Determination of Formononetin, Calycosin and Rhamnocitrin from Astragalus Complanatus by UHPLC-MS-MS in Rat Plasma: Application to a Pharmacokinetic Study. J Chromatogr Sci. 2016 Jun 19.|[2]Hong JT, et al. Regulation of heme oxygenase-1 expression and MAPK pathways in response to kaempferol and rhamnocitrin in PC12 cells. Toxicol Appl Pharmacol. 2009 May 15;237 (1) :59-68.|[3]Lin T, et al. Rhamnocitrin extracted from Nervilia fordii inhibited vascular endothelial activation via miR-185/STIM-1/SOCE/NFATc3. Phytomedicine. 2020 Dec;79:153350.|[4]GU, Qiuli, et al. A preliminary study on anti-inflammatory effects of rhamnocitrin from Oxytropis falcata Bunge. Chinese Journal of Information on Traditional Chinese Medicine (2014) : 48-50.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, protect from light)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [569-92-6]