2'-Acetylacteoside (Standard)
2'-Acetylacteoside (Standard) is the analytical standard of 2'-Acetylacteoside (2'-AA) (HY-N0026). This product is intended for research and analytical applications. 2'-Acetylacteoside is a natural compound with oral activity and blood-brain barrier permeability. 2'-Acetylacteosideexhibits MAO‑B inhibitory activity (IC50 = 17.71 μM, Ki = 13.81 μM). 2'-Acetylacteoside downregulates the expression of RANK, TRAF6, NF‑κB, NFATc1 and IKKβ, disrupts the RANKL/RANK interaction, blocks downstream signaling pathways, and increases the level of phosphorylated Akt. 2'-Acetylacteoside possesses potent anti-osteoclastogenic, anti-bone resorptive, pro-neurogenic, neuroprotective and antioxidant activities. 2'-Acetylacteoside can be used in the research of osteoporosis, ischemic stroke and Parkinson's disease.
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- CAS No.: 94492-24-7
- Formule: C31H38O16
- Masse moléculaire:666.62
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Product Information
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Chemical Information
- Pureté et documentation
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Help & FAQs
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HY-N0026
2'-AcetylacteosideNatural Compound -
HY-N0022
IsoacteosideNatural Product -
HY-N0528
LinarinAChE Inhibitor -
HY-103596
Thalidomide-4-OHCereblon Ligand -
HY-W015600
2-AcetamidophenolFerroptosis Regulator -
HY-N1067
XanthohumolCOX Inhibitor -
HY-N0015
AstragalinNF-κB Inhibitor -
HY-N0791
TectoridinPhytoestrogen -
HY-N0367
Trans-AnetholeEndogenous Metabolite -
HY-N0321
Caftaric acidAnti-apoptotic Agent -
HY-N0791R
Tectoridin (Standard)Phytoestrogen
Product Information
Information
Application
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 94492-24-7
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Masse moléculaire 666.62
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Formule C31H38O16
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SMILES
OC1=CC=C(/C=C/C(O[C@H]2[C@H](O[C@]3([H])O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](OC(C)=O)[C@H](OCCC4=CC=C(O)C(O)=C4)O[C@@H]2CO)=O)C=C1O
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Synonyms
2'-AA (Standard)
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Structure Classification
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Initial Source
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[1]. Li Y, Li N, Zhao X, et al. Beneficial effect of 2'-acetylacteoside on ovariectomized mice via modulating the function of bone resorption. Biomed Pharmacother. 2020;131:110747. [Content Brief]
[2]. Wang M, et al. 2-Acetylacteoside improves recovery after ischemic stroke by promoting neurogenesis via the PI3K/Akt pathway. Free Radic Biol Med. 2024;225:415-429. [Content Brief]
[3]. Zhai X, et al. Evaluation of the Neuroprotective Effect of Total Glycosides of Cistanche deserticola and Investigation of Novel Brain-Targeting Natural MAO-B Inhibitors. ACS Chem Neurosci. 2024 Dec 18;15(24):4544-4558. [Content Brief]
[4]. He ZD, et al. Antioxidant activity of phenylethanoid glycosides from Brandisia hancei. J Ethnopharmacol. 2000 Aug;71(3):483-6. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
2'-Acetylacteoside (Standard) Related Classifications
HY-N0026R Related Classifications
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