6-Hydroxyflavone

CAT:
804-HY-N7110-01
Size:
100 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
6-Hydroxyflavone - image 1

6-Hydroxyflavone

  • Description :

    6-Hydroxyflavone is an orally effective flavonoid compound. 6-Hydroxyflavone can inhibit LPS (HY-D1056) -induced NO production and has anti-inflammatory effects. 6-Hydroxyflavone promotes osteoblast differentiation by activating AKT, ERK 1/2 and JNK signaling pathways. 6-Hydroxyflavone has an inhibitory effect on bovine hemoglobin (BHb) glycosylation. 6-Hydroxyflavone has a kidney protective effect. In addition, 6-Hydroxyflavone enhances GABA-induced current through the Benzodiazepine sites of γ-aminobutyric acid (GABAA) receptors. 6-Hydroxyflavone shows a clear preference for α2 - and α3 - subtypes, which play an anti-anxiety role[1][2][3][4][5][6].
  • UNSPSC :

    12352005
  • Hazard Statement :

    H315, H319
  • Target :

    Akt; ERK; GABA Receptor; JNK
  • Type :

    Natural Products
  • Related Pathways :

    MAPK/ERK Pathway; Membrane Transporter/Ion Channel; Neuronal Signaling; PI3K/Akt/mTOR; Stem Cell/Wnt
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Metabolic Disease; Inflammation/Immunology; Neurological Disease
  • Assay Protocol :

    https://www.medchemexpress.com/6-hydroxyflavone.html
  • Purity :

    99.92
  • Solubility :

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

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

    C15H10O3
  • Molecular Weight :

    238.24
  • Precautions :

    H315, H319
  • References & Citations :

    [1]Das S, et al. Characterization of non-covalent binding of 6-hydroxyflavone and 5,7-dihydroxyflavone with bovine hemoglobin: Multi-spectroscopic and molecular docking analyses. J Photochem Photobiol B. 2018 Jan;178:40-52.|[2]Lai CH, et al. Effects of 6-Hydroxyflavone on Osteoblast Differentiation in MC3T3-E1 Cells. Evid Based Complement Alternat Med. 2014;2014:924560.|[3]Wang X, et al. 6-Hydroxyflavone and derivatives exhibit potent anti-inflammatory activity among mono-, di- and polyhydroxylated flavones in kidney mesangial cells. PLoS One. 2015 Mar 19;10 (3) :e0116409.|[4]Din ZU, et al. The flavonoid 6-hydroxyflavone prevention of cisplatin-induced nephrotoxicity. Histol Histopathol. 2020 Oct;35 (10) :1197-1209.|[5]Ren L, et al. GABA (A) receptor subtype selectivity underlying anxiolytic effect of 6-hydroxyflavone. Biochem Pharmacol. 2010 May 1;79 (9) :1337-44.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Natural Products
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [6665-83-4]

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