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Atomfair (+/-)-Huperzine A Fordine C15H18N2O
Description (+/-)-Huperzine A (CAS No. 120786-18-7) is a highly purified racemic alkaloid derived from the Chinese club moss Huperzia serrata . With the molecular formula C15H18N2O and IUPAC name 1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one, this compound is a potent, reversible acetylcholinesterase inhibitor with demonstrated neuroprotective properties. Provided as a white to off-white crystalline powder, our (+/-)-Huperzine A is ??98% pure by HPLC analysis, making it ideal for neuroscience research, pharmacological studies, and drug discovery applications. The product is supplied in amber glass vials under inert atmosphere to ensure stability and is suitable for in vitro and in vivo studies. Store at -20??C protected from…
Description
Description
(+/-)-Huperzine A (CAS No. 120786-18-7) is a highly purified racemic alkaloid derived from the Chinese club moss Huperzia serrata. With the molecular formula C15H18N2O and IUPAC name 1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one, this compound is a potent, reversible acetylcholinesterase inhibitor with demonstrated neuroprotective properties. Provided as a white to off-white crystalline powder, our (+/-)-Huperzine A is ??98% pure by HPLC analysis, making it ideal for neuroscience research, pharmacological studies, and drug discovery applications. The product is supplied in amber glass vials under inert atmosphere to ensure stability and is suitable for in vitro and in vivo studies. Store at -20??C protected from light and moisture.
- CAS No: 120786-18-7
- Molecular Formula: C15H18N2O
- Molecular Weight: 242.32
- Exact Mass: 242.141913202
- Monoisotopic Mass: 242.141913202
- IUPAC Name: 1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one
- SMILES: CC=C1C2CC3=C(C1(CC(=C2)C)N)C=CC(=O)N3
- Synonyms: 120786-18-7, (+/-)-Huperzine A, Fordine, 103735-86-0, (+/-)Huperzine A
Application
(+/-)-Huperzine A is widely used in neuroscience research as a reference standard for acetylcholinesterase inhibition studies. It serves as a valuable tool compound for investigating Alzheimer’s disease mechanisms and potential therapeutic approaches. Researchers utilize this racemic form to study stereospecificity in cholinesterase inhibition and compare efficacy with enantiopure forms. The compound has also shown promise in models of cognitive enhancement and neuroprotection.
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