Linarin

• Description:

  Linarin (Buddleoside) is an orally active and selective inhibitor of acetylcholinesterase (AChE) . Linarin has many activities, such as anti-inflammatory, antioxidant, sleep aid and sedation, bone differentiation, anti-tumor, antibacterial and antiviral. Linarin can be used to study diseases such as the nervous system, osteoporosis and cancer[1][2][3][4].

• Product Name Alternative:

  Buddleoside; Linarine

• UNSPSC:

  12352005

• Hazard Statement:

  H302, H315, H319, H335

• Target:

  Apoptosis; Bacterial; Cholinesterase (ChE) ; HIV; Influenza Virus; PKA; TNF Receptor

• Type:

  Natural Products

• Related Pathways:

  Anti-infection; Apoptosis; Neuronal Signaling; Stem Cell/Wnt; TGF-beta/Smad

• Applications:

  Neuroscience-Neuromodulation

• Field of Research:

  Cancer; Infection; Inflammation/Immunology; Neurological Disease

• Assay Protocol:

  https://www.medchemexpress.com/linarin.html

• Purity:

  98.02

• Solubility:

  DMSO : 250 mg/mL (ultrasonic)

• Smiles:

  O=C(C=C(C1=CC=C(OC)C=C1)OC2=CC(O[C@@H]([C@@H]([C@@H](O)[C@@H]3O)O)O[C@@H]3CO[C@H](O[C@@H](C)[C@H](O)[C@H]4O)[C@@H]4O)=C5)C2=C5O

• Molecular Formula:

  C28H32O14

• Molecular Weight:

  592.55

• Precautions:

  H302, H315, H319, H335

• References & Citations:

  [1]Päivi P. Oinonen, etc. Linarin, a selective acetylcholinesterase inhibitor from Mentha arvensis, Fitoterapia, Volume 77, Issue 6, 2006, Pages 429-434, ISSN 0367-326X|[2]Mottaghipisheh J, et al. Linarin, a Glycosylated Flavonoid, with Potential Therapeutic Attributes: A Comprehensive Review. Pharmaceuticals (Basel) . 2021 Oct 29;14 (11) :1104.|[3]Singh RP, et al. Acacetin inhibits cell growth and cell cycle progression, and induces apoptosis in human prostate cancer cells: structure-activity relationship with linarin and linarin acetate. Carcinogenesis. 2005 Apr;26 (4) :845-54.|[4]Li J, et al. Linarin promotes osteogenic differentiation by activating the BMP-2/RUNX2 pathway via protein kinase A signaling. Int J Mol Med. 2016 Apr;37 (4) :901-10.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  4°C (Powder, protect from light)

• Scientific Category:

  Natural Products

• Clinical Information:

  No Development Reported

• Isoform:

  AChE

• CAS Number:

  [480-36-4]