SMB01010

Marrubiin

≥90% (LC/MS-ELSD)

• Synonim(y): (1R,4S,8S,9R,10R,12R)-9-[2-(furan-3-yl)ethyl]-9-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one
• Wzór empiryczny (zapis Hilla): C₂₀H₂₈O₄
• Numer CAS: 465-92-9
• Masa cząsteczkowa: 332.43
• UNSPSC Code: 12352205
• NACRES: NA.25
• MDL number: MFCD08461003

Właściwości

• biological source: plant
• assay: ≥90% (LC/MS-ELSD)
• form: solid
• mol wt: 332.43
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: −20°C
• SMILES string: [o]1cc(cc1)CC[C@@]2([C@@]3([C@H]4[C@H](OC(=O)[C@]4(CCC3)C)C[C@H]2C)C)O
• InChI: 1S/C20H28O4/c1-13-11-15-16-18(2,17(21)24-15)7-4-8-19(16,3)20(13,22)9-5-14-6-10-23-12-14/h6,10,12-13,15-16,22H,4-5,7-9,11H2,1-3H3/t13-,15-,16+,18+,19+,20-/m1/s1
• InChI key: HQLLRHCTVDVUJB-OBHOOXMTSA-N

Opis

General description

Marrubiin is a labdanoid lactone commonly derived from Marrubium Sp. plants, including M. globosum, M. alysson, M. vulgare, and M. anisodon. Existing research suggests that this plant-derived metabolite possesses various biological properties, including antioxidant, antifungal, gastroprotective, immunomodulatory, cardioprotective, anti-diabetic, and analgesic activities.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Biochem/physiol Actions

Based on existing research, Marrubiin has demonstrated the ability to inhibit the production of pro-inflammatory cytokines and reduce the activity of enzymes involved in oxidative stress. Additionally, it has been observed to lower blood pressure and provide protection against ischemic heart injury.

Features and Benefits

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Other Notes

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Informacja o środkach bezpieczeństwa

• pictograms: GHS06
• signalword: Danger
• hcodes: H301
• pcodes: P264 - P270 - P301 + P310 - P405 - P501
• Hazard Classifications: Acute Tox. 3 Oral
• Klasa składowania: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable