Lactupicrin

CAT:
804-HY-N8290-01
Size:
10 mM - 1 mL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Lactupicrin - image 1

Lactupicrin

  • Description :

    Lactupicrin (Lactucopicrin) exhibits analgesic, sedative, antimalarial activities and atheroprotective effect. Lactupicrin inhibits acetylcholinesterase (AChE) with an IC50 of 150.3 μM. Lactupicrin is an orally active characteristic bitter sesquiterpene lactone[1][2][3][4][5].
  • Product Name Alternative :

    Lactucopicrin
  • UNSPSC :

    12352005
  • Hazard Statement :

    H317
  • Target :

    Cholinesterase (ChE) ; LOX-1; NF-κB; Parasite
  • Type :

    Natural Products
  • Related Pathways :

    Anti-infection; Metabolic Enzyme/Protease; Neuronal Signaling; NF-κB
  • Applications :

    Metabolism-protein/nucleotide metabolism
  • Field of Research :

    Infection; Inflammation/Immunology; Neurological Disease; Cardiovascular Disease
  • Assay Protocol :

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

    99.97
  • Solubility :

    DMSO : 250 mg/mL (ultrasonic)
  • Smiles :

    OCC([C@](C1=C2C)([H])[C@](OC3=O)([H])[C@@](C3=C)([H])[C@H](C2)OC(CC(C=C4)=CC=C4O)=O)=CC1=O
  • Molecular Formula :

    C23H22O7
  • Molecular Weight :

    410.42
  • Precautions :

    H317
  • References & Citations :

    [1]Wesołowska A, et, al. Analgesic and sedative activities of lactucin and some lactucin-like guaianolides in mice. J Ethnopharmacol. 2006 Sep 19;107 (2) :254-8.|[2]Li Q, et, al. Terpene Lactucopicrin Limits Macrophage Foam Cell Formation by a Reduction of Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1 in Lipid Rafts. Mol Nutr Food Res. 2022 Feb;66 (4) :e2100905. |[3]He L, et al. Lactupicrin Inhibits Cytoplasmic Dynein-Mediated NF-κB Activation in Inflammated Macrophages and Alleviates Atherogenesis in Apolipoprotein E-Deficient Mice. Mol Nutr Food Res. 2021 Feb;65 (4) :e2000989. |[4] Bischoff TA, et al. Antimalarial activity of lactucin and lactucopicrin: sesquiterpene lactones isolated from Cichorium intybus L. J Ethnopharmacol. 2004 Dec;95 (2-3) :455-7. |[5]Rollinger JM, et al. Application of the in combo screening approach for the discovery of non-alkaloid acetylcholinesterase inhibitors from Cichorium intybus. Curr Drug Discov Technol. 2005 Sep;2 (3) :185-93.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Natural Products
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [65725-11-3]

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