SMB01084

Sphaerobioside

≥90% (LC/MS-ELSD)

• Sinonimo/i: 7-[[6-O-(6-Deoxy-?-L-mannopyranosyl)-?-D-glucopyranosyl]oxy]-5-hydroxy-3-(4-hydroxyph enyl)-4H-1-benzopyran-4-one, Genistein-7-rhamnoglucoside, Hirsutissimiside B
• Formula empirica (notazione di Hill): C₂₇H₃₀O₁₄
• Numero CAS: 14988-20-6
• Peso molecolare: 578.52
• Codice UNSPSC: 12352205
• NACRES: NA.25

Proprietà

• Origine biologica: plant
• Saggio: ≥90% (LC/MS-ELSD)
• Stato: solid
• PM: 578.52
• applicazioni: metabolomics; vitamins, nutraceuticals, and natural products
• Temperatura di conservazione: −20°C
• Stringa SMILE: O1[C@H]([C@@H]([C@@H]([C@H]([C@@H]1C)O)O)O)OC[C@H]2O[C@H]([C@@H]([C@H]([C@@H]2O)O)O)Oc3cc4c(c(c3)O)C(=O)C(=CO4)c5ccc(cc5)O
• InChI: 1S/C27H30O14/c1-10-19(30)22(33)24(35)26(39-10)38-9-17-21(32)23(34)25(36)27(41-17)40-13-6-15(29)18-16(7-13)37-8-14(20(18)31)11-2-4-12(28)5-3-11/h2-8,10,17,19,21-30,32-36H,9H2,1H3/t10-,17+,19-,21+,22+,23-,24+,25+,26+,27+/m0/s1; XIQCIPHUIZGDLB-SEPMLUPWSA-N

Descrizione

Descrizione generale

Sphaerobioside, an isoflavonoid glycoside, serves as a secondary metabolite found in several plant species, such as Riosema tuberosum, Baptisia sphaerocarpa, Sphaerophysa salsula, Sphaeranthus indicus, and Sphaeranthus africanus. This compound possesses a diverse range of properties, including anti-inflammatory, antioxidant, antimicrobial, and anticancer characteristics.

Applicazioni

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

Azioni biochim/fisiol

Sphaerobioside′s mode of action includes the inhibition of multiple enzymes and signaling pathways. It has been observed to suppress the activity of cyclooxygenase-2 (COX-2), an enzyme pivotal in the inflammatory response. Additionally, Sphaerobioside hinders the activation of nuclear factor-kappa B (NF-κB), a transcription factor that plays a crucial role in regulating inflammation and the immune response. It can also trigger apoptosis and hinder cell proliferation in multiple cancer cell lines, as well as exhibit neuroprotective qualities, showing promise in enhancing cognitive function in animal models of Alzheimer′s disease.

Caratteristiche e vantaggi

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

Altre note

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Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable