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Jaceosidin

Jaceosidin Structure
Jaceosidin
  • CAS No.18085-97-7
  • Chemical Name:Jaceosidin
  • CBNumber:CB51515205
  • Molecular Formula:C17H14O7
  • Formula Weight:330.29
  • MOL File:18085-97-7.mol
Jaceosidin Property
  • Melting point 259-260 °C
  • Boiling point 619.0±55.0 °C(Predicted)
  • Density 1.483±0.06 g/cm3(Predicted)
  • storage temp. 2-8°C(protect from light)
  • solubility DMSO (Slightly), Methanol (Slightly, Sonicated), Pyridine (Slightly)
  • form Solid
  • pka 6.47±0.40(Predicted)
  • color Pale Yellow to Light Yellow
  • Stability Hygroscopic
  • LogP 1.300 (est)
  • EWG's Food Scores 1
  • FDA UNII 5U4Y68G678
  • UNSPSC Code 41116107
  • NACRES NA.24
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H315-H319
  • Precautionary statements P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Jaceosidin Chemical Properties,Usage,Production

  • Uses Jaceosidin exhibits anti-allergic, anti-inflammatory and apoptosis inducing activities.
  • Definition ChEBI: A trihydroxyflavone that is flavone with hydroxy groups at positions 5, 7 and 4' and methoxy groups at positions 3' and 6. Isolated from Salvia tomentosa and Artemisia asiatica, it exhibits anti-allergic, anti-inflammatory and apo tosis inducing activties.
  • in vivo

    Jaceosidin (10 and 20 mg/kg, p.o., once a day for 3 days) blocks carrageenan-induced increase in leukocyte number and protein levels in air pouch exudates in mice[3].
    ? Jaceosidin (10, 20 mg/kg, p.o.) suppresses COX-2 expression and NF-κB activation in mice[3].
    ? Jaceosidin (20 mg/kg, p.o. for 2 hours) reduces hind paw edema volume in rats[3].

    Animal Model:5-week-old male BALB/c mice (23-26 g)[3]
    Dosage:10 and 20 mg/kg
    Administration:P.O. once a day for 3 days
    Result:Decreased the volumes of exudates (inflammatory markers), cell number and protein levels. Inhibited TNF-α by 46.7% and 50.8%, IL-1β by 46.0% and 44.7%, and PGE2 by 21.7% and 16.9%, respectively, at 20 mg/kg. Blocked COX-2 expression and NF-κB activation.
    Animal Model:Male Sprague-Dawley rats (180-200 g)[3]
    Dosage:20 mg/kg
    Administration:P.O., for 2 hour
    Result:Reduced hind paw edema volume by 27.1% at 1 h, and 24.0% at 2 h, respectively.
  • IC 50 Bax; COX-2
Jaceosidin Preparation Products And Raw materials
Raw materials
Preparation Products
Global(190)Suppliers
  • Supplier:
    Hangzhou ICH Biofarm Co., Ltd
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    Henan Tianfu Chemical Co.,Ltd.
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