Bornyl acetate
Bornyl acetate (CAS No.: 76-49-3) is a bicyclic monoterpene ester widely classified as a natural volatile phytochemical and aroma constituent that occurs predominantly in conifer essential oils and in several medicinal plant matrices, where it is investigated in life sciences as a bioactive small molecule for inflammation and stress response biology, chemical ecology, and natural product inspired hit identification; current preclinical literature generally characterizes this compound as showing anti inflammatory and cytomodulatory activity profiles in biochemical and cellular systems, with reported mechanisms commonly inferred from modulation of pro inflammatory mediator networks such as reduced nitric oxide and prostaglandin associated signaling, attenuation of cytokine release patterns, and regulation of canonical pathways including NF kappa B and MAPK related signaling axes in stimulus responsive models, while antineoplastic related observations are typically treated as exploratory phenotypic findings requiring target deconvolution and orthogonal validation; because publicly described studies are heterogeneous in assay format and endpoint definitions, activity is most appropriately summarized as occurring across broad micromolar to low millimolar experimental windows rather than a single standardized potency metric, and in vitro workflows often employ macrophage like, epithelial, or tumor derived cell systems to evaluate inflammatory transcriptional readouts, oxidative stress markers, and viability linked phenotypes, whereas in vivo research commonly uses rodent inflammation or injury associated paradigms to examine biomarker and histopathology trends under protocol specific dosing regimens, with the concentrations or doses used in experiments typically depending on specific experimental designs and research objectives; in drug discovery settings, bornyl acetate is therefore best positioned as a natural product reference scaffold for mechanism guided screening, combination profiling, and structure activity relationship expansion within nonclinical research programs.
| Storage | -20°C for 2 years |
| M.Wt | 196.29 |
| Cas No. | 76-49-3 |
| Formula | C12H20O2 |
| Canonical SMILES | CC1(C)[C@@]2(C)[C@H](OC(C)=O)C[C@]1([H])CC2 |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |






