Iriflophenone 3-C-glucoside - ≥98% , CAS No.104669-02-5

CAS: 104669-02-5 Cat. No.: I413424 Peso molecular: 408.36

GRADE & PURITY ≥98%

Synonyms

DTXSID00904231 | MEGxp0_001276 | AKOS040733463 | HY-N4008 | Iriflophenone 3-C--D-glucopyranoside | Iriflophenone 3-C-glucoside | NCGC00180623-01 | Iriflophenone 3-C-b-D-glucopyranoside | MS-27007 | MFCD20260926 | (4-hydroxyphenyl)-[2,4,6-trihydroxy-3-[(2S

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Information

Iriflophenone 3-C-glucoside (Iriflophenone 3-C-β-D-glucopyranoside, Iriflophenone 3-C-b-D-glucopyranoside), isolated from Cyclopia genistoides, exhibits antioxidant activity.

Specifications

Sinónimos

DTXSID00904231 | MEGxp0_001276 | AKOS040733463 | HY-N4008 | Iriflophenone 3-C--D-glucopyranoside | Iriflophenone 3-C-glucoside | NCGC00180623-01 | Iriflophenone 3-C-b-D-glucopyranoside | MS-27007 | MFCD20260926 | (4-hydroxyphenyl)-[2, 4, 6-trihydroxy-3-[(2S

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Iriflophenone 3-C-glucoside (Iriflophenone 3-C-β-D-glucopyranoside, Iriflophenone 3-C-b-D-glucopyranoside), isolated from Cyclopia genistoides, exhibits antioxidant activity.

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: C1=CC(=CC=C1C(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O
• IUPAC Name: (4-hydroxyphenyl)-[2,4,6-trihydroxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]methanone
• InChIKey: BZYKNVLTMWYEFA-ZJKJAXBQSA-N
• INCHI: 1S/C19H20O10/c20-6-11-15(25)17(27)18(28)19(29-11)13-10(23)5-9(22)12(16(13)26)14(24)7-1-3-8(21)4-2-7/h1-5,11,15,17-23,25-28H,6H2/t11-,15-,17+,18-,19+/m1/s1
• Isómeros SMILES: C1=CC(=CC=C1C(=O)C2=C(C=C(C(=C2O)[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O)O
• Peso molecular: 408.36
• Reaxy-Rn: 45226307
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=45226307&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Phenolic glycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Phenolic glycosides
• Alternative Parents: Benzophenones Aryl-phenylketones Diphenylmethanes C-glycosyl compounds Phloroglucinols and derivatives Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Monosaccharides Oxanes Vinylogous acids Secondary alcohols Oxacyclic compounds Polyols Dialkyl ethers Organic oxides Hydrocarbon derivatives Primary alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Phenolic glycoside - Benzophenone - Diphenylmethane - Aryl-phenylketone - C-glycosyl compound - Phloroglucinol derivative - Benzenetriol - Benzoyl - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monocyclic benzene moiety - Monosaccharide - Vinylogous acid - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Dialkyl ether - Polyol - Ether - Primary alcohol - Organic oxide - Hydrocarbon derivative - Alcohol - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: DMSO: 11 mg/mL (26.94 mM)
• Sensibilidad: Light sensitive
• Peso molecular: 408.400 g/mol
• XLogP3: -0.100
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 4
• Exact Mass: 408.106 Da
• Monoisotopic Mass: 408.106 Da
• Topological Polar Surface Area: 188.000 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 565.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1