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  • (+)-Borneol
(+)-Borneol的可视化放大

(+)-Borneol

A bicyclic monoterpene with diverse biological activities

价格
0-440
(+)-Borneol的二维码

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  • 货号: ajce54150
  • CAS: 464-43-7
  • 别名: (+)-冰片
  • 分子式: C10H18O
  • 分子量: 154.25
  • 纯度: >98%
  • 溶解度: DMSO: ≥ 100 mg/mL (648.30 mM); Water: < 0.1 mg/mL (insoluble)
  • 储存: Store at -20°C
  • 库存: 现货

Background

(+)-Borneol is a bicyclic monoterpene and a stereoisomer of (–)-borneol that has been found in various plants, including S. tomentosa, and has diverse biological activities including analgesic, neuroprotective, antioxidant, and antimicrobial properties.1,2,3,4 (+)-Borneol is a positive allosteric modulator of α1β2γ2L subunit-containing GABAA receptors (EC50 = 248 μM for human recombinant receptors).1 It dose-dependently increases the paw withdrawal threshold following segmental spinal nerve ligation surgery or intraplantar injection of complete Freund's adjuvant (CFA) in mouse paw.2 (+)-Borneol (100 μM) inhibits increases in reactive oxygen species (ROS) levels and cytotoxicity in SH-SY5Y neuroblastoma cells incubated with amyloid-β (1-42) .3 It also inhibits the growth of Gram-positive and Gram-negative bacteria in vitro, including E. coli, S. aureus, P. aeruginosa, P. vulgaris, and S. typhimurium (MICs = 125-250 μg/mL).4 Formulations containing (+)-borneol have been used as fragrance ingredients.


1.Granger, R.E., Campbell, E.L., and Johnston, G.A.R.(+)- And (–)-borneol: Efficacious positive modulators of GABA action at human recombinant α1β2γ2L GABAA receptorsBiochem. Pharmacol.69(7)1101-1111(2005) 2.Jiang, J., Shen, Y.Y., Li, J., et al.(+)-Borneol alleviates mechanical hyperalgesia in models of chronic inflammatory and neuropathic pain in miceEur. J. Pharmacol.75753-58(2015) 3.Hur, J., Pak, S.C., Koo, B.S., et al.Borneol alleviates oxidative stress via upregulation of Nrf2 and Bcl-2 in SH-SY5Y cellsPharm. Biol.51(1)30-35(2013) 4.Tabanca, N., Kirimer, N., Demirci, B., et al.Composition and antimicrobial activity of the essential oils of Micromeria cristata subsp. phrygia and the enantiomeric distribution of borneolJ. Agric. Food Chem.49(9)4300-4303(2001)

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