[{"data":1,"prerenderedAt":23},["ShallowReactive",2],{"notifications-general-de":3,"compound-BORN-de":4},"Wegen der Sommerferien arbeitet das Labor vom 22. Juli bis 9. August 2026 nach einem geänderten Zeitplan. Analyseergebnisse sind 7 bis 10 Tage nach Proben­eingang verfügbar. Vielen Dank für Ihr Verständnis.",{"name":5,"shortname":6,"synonyms":7,"cas":8,"molMass":9,"pubchemLink":10,"structure":11,"important":12,"synthetic":13,"compoundClass":14,"asociationImage":17,"summarySet":18,"compoundEffectSet":22},"Borneol","BORN","Isoborneol, (-)-Borneol","507-70-0",154.25,"https:\u002F\u002Fpubchem.ncbi.nlm.nih.gov\u002Fcompound\u002F64685","science\u002Fstructures\u002FBORN.png",true,false,{"id":15,"description":16},"1","Terpenoids","science\u002Fimages\u002Fcamphor-tree-g1c2bc3d8d_1920.jpg",[19],{"summaryText":20,"language":21},"\u003Cp>\u003Cspan style=\"background-color: rgb(255, 255, 255);\">\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">Borneol is a bicyclic organic compound and a terpene derivative, which can be found in several species of \u003C\u002Fspan>\u003Ci>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">Heterotheca, Artemisia, Callicarpa, Dipterocarpaceae, Blumea balsamifera\u003C\u002Fspan>\u003C\u002Fi>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> and \u003C\u002Fspan>\u003Ci>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">Kaempferia galanga\u003C\u002Fspan>\u003C\u002Fi>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">. \u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">The \u003C\u002Fspan>\u003Cspan style=\"background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; overflow-wrap: break-word; font-family: "Times New Roman"; font-size: 14px;\">hydroxyl\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> group in this compound is placed in an \u003C\u002Fspan>\u003Ci style=\"font-family: sans-serif;\">\u003Cspan style=\"background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; overflow-wrap: break-word; font-family: "Times New Roman"; font-size: 14px;\">endo\u003C\u002Fspan>\u003C\u002Fi>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> position. The exo diastereomer is called \u003C\u002Fspan>\u003Cspan style=\"background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; overflow-wrap: break-word; font-family: "Times New Roman"; font-size: 14px;\">isoborneol\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">. Being chiral, borneol exists as \u003C\u002Fspan>\u003Cspan style=\"background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; overflow-wrap: break-word; font-family: "Times New Roman"; font-size: 14px;\">enantiomers\u003C\u002Fspan>\u003Cspan style=\"font-family: sans-serif;\">\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">, both of which are found in nature.\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> \u003C\u002Fspan>\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">Whereas \u003C\u002Fspan>\u003Ci style=\"font-family: sans-serif;\">\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">d\u003C\u002Fspan>\u003C\u002Fi>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">-borneol was the \u003C\u002Fspan>\u003Cfont face=\"sans-serif\">\u003Cspan style=\"background-image: none; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-family: "Times New Roman"; font-size: 14px;\">enantiomer\u003C\u002Fspan>\u003C\u002Ffont>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\"> that used to be the most readily available commercially, the more commercially available enantiomer now is \u003C\u002Fspan>\u003Ci style=\"font-family: sans-serif;\">\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">l\u003C\u002Fspan>\u003C\u002Fi>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">-borneol, which also occurs in nature. \u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"background-color: rgb(255, 255, 255);\">\u003Cspan style=\"font-family: sans-serif;\">\u003Cbr>\u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px;\">It has potential anticancer, antibacterial and antiinflamation effects. \u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px; white-space-collapse: preserve;\">Borneol is known for its ability to enhance the permeability of cell membranes. This property has been exploited in pharmacology to improve the absorption of certain drugs, especially those with poor bioavailability. Borneol acts as a penetration enhancer and can facilitate the delivery of drugs through the skin or mucous membranes. \u003C\u002Fspan>\u003Cspan style=\"font-family: "Times New Roman"; font-size: 14px; white-space-collapse: preserve;\">Some studies suggest that borneol may have neuroprotective effects. It has been investigated for its potential in the treatment of neurological disorders such as Alzheimer's disease. Its ability to cross the blood-brain barrier makes it a valuable candidate for drug delivery to the central nervous system.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",null,[],1785925846707]