CAS 97938-30-2

Sophoraflavanona G

Descripción:

Sophoraflavanona G es un compuesto flavonoide derivado principalmente del género de plantas Sophora, particularmente de Sophora flavescens. Se caracteriza por su estructura química única, que incluye un esqueleto de flavanona, lo que contribuye a sus posibles actividades biológicas. Este compuesto exhibe diversas propiedades farmacológicas, incluyendo efectos antiinflamatorios, antioxidantes y anticancerígenos, lo que lo hace de interés en la química medicinal y la investigación de productos naturales. Sophoraflavanona G se encuentra típicamente en forma de un sólido cristalino amarillento y es soluble en disolventes orgánicos. Su fórmula molecular refleja la presencia de múltiples grupos hidroxilo, que son responsables de su reactividad e interacción con sistemas biológicos. La investigación sobre Sophoraflavanona G continúa explorando sus mecanismos de acción y aplicaciones terapéuticas potenciales, particularmente en el contexto de enfermedades crónicas y condiciones relacionadas con el estrés oxidativo. Al igual que muchos flavonoides, su biodisponibilidad y vías metabólicas también son temas de investigación en curso, destacando la complejidad de sus efectos in vivo.

Fórmula: C₂₅H₂₈O₆

InChI: InChI=1S/C25H28O6/c1-13(2)5-6-15(14(3)4)9-18-20(28)11-21(29)24-22(30)12-23(31-25(18)24)17-8-7-16(26)10-19(17)27/h5,7-8,10-11,15,23,26-29H,3,6,9,12H2,1-2,4H3/t15-,23+/m1/s1

Clave InChI: InChIKey=XRYVAQQLDYTHCL-CMJOXMDJSA-N

SMILES: C([C@@H](CC=C(C)C)C(C)=C)C1=C2C(C(=O)C[C@H](O2)C3=C(O)C=C(O)C=C3)=C(O)C=C1O

Sinónimos:

• (-)-Vexibinol
• (2S)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-yl]-4H-1-benzopyran-4-one
• 4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-yl]-, (2S)-
• 4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexenyl]-, (2S)-
• 4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[5-methyl-2-(1-methylethenyl)-4-hexenyl]-, [S-(R*,S*)]-
• 4H-1-benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-6-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-yl]-, (2S)-
• Kushenol F
• Kushnol F
• Norkurarinone
• Sophoraflavanone G
• (2S)-2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2,3-dihydro-4H-chromen-4-one

Sophoraflavanone G

CAS: 97938-30-2

Sophoraflavanone G

Fórmula: C₂₅H₂₈O₆

Pureza: 99.5%

Peso molecular: 424.49

Ref: 54-BUP08940

Kushenol F

CAS: 97938-30-2

Fórmula: C₂₅H₂₈O₆

Pureza: 95%~99%

Peso molecular: 424.493

Ref: BP-BP0835

Sophoraflavanone G (Standard)

CAS: 97938-30-2

Sophoraflavanone G (Standard) is a reference standard for research and analysis in studies involving Sophoraflavanone G. Sophoraflavanone G (Kushenol F) (Kushenol F), isolated from Sophora flavescens, induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related pathways.

Fórmula: C₂₅H₂₈O₆

Peso molecular: 424.49

Ref: TM-TMSM-1920

Sophoraflavanone G

CAS: 97938-30-2

Fórmula: C₂₅H₂₈O₆

Pureza: 99%

Forma y color: Solid

Peso molecular: 424.4862

Ref: IN-DA005XAK

Sophoraflavanone G

CAS: 97938-30-2

Fórmula: C₂₅H₂₈O₆

Pureza: ≥ 98.0%

Forma y color: White to off-white powder

Peso molecular: 424.49

Ref: 7W-GY8573

Sophoraflavanone G

CAS: 97938-30-2

Sophoraflavanone G (Kushenol F) (Kushenol F), isolated from Sophora flavescens, induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related

Fórmula: C₂₅H₂₈O₆

Pureza: 97.09% - 99.77%

Forma y color: Solid

Peso molecular: 424.4862

Ref: TM-T5S1000

Sophoraflavanone G

CAS: 97938-30-2

Oxygen-heterocyclic compound

Fórmula: C₂₅H₂₈O₆

Pureza: ≥ 95.0 % (HPLC)

Forma y color: Powder

Peso molecular: 424.5

Ref: 5G-83544

Norkurarinone

CAS: 97938-30-2

Norkurarinone is a natural compound that inhibits the growth of bacteria. It has been shown to inhibit the production of inflammatory mediators, such as prostaglandins and leukotrienes, in vitro. In addition, norkurarinone has been shown to have protective effects against oxidative stress and some metabolic disorders. Norkurarinone has also been shown to be effective against Gram-positive and Gram-negative bacteria, as well as yeast. The optimum concentration for inhibition is 0.3 μg/mL.
The chemical structure of norkurarinone is similar to sophoraflavanones found in Sophora flavescens leaves, which may contribute to its antimicrobial activity.

Fórmula: C₂₅H₂₈O₆

Pureza: Min. 95%

Forma y color: White Powder

Peso molecular: 424.49 g/mol

Ref: 3D-FN74220

Sophoraflavanone G

CAS: 97938-30-2

Fórmula: C₂₅H₂₈O₆

Peso molecular: 424.5

Ref: BE-RMT12318

Vexibinol

CAS: 97938-30-2

(S)-2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one

Fórmula: C₂₅H₂₈O₆

Pureza: 99%

Peso molecular: 424.49

Ref: IN-DG298349