CAS 97938-30-2

Sophoraflavanone G

Descrizione:

Sophoraflavanone G è un composto flavonoide derivato principalmente dal genere di piante Sophora, in particolare da Sophora flavescens. È caratterizzato dalla sua unica struttura chimica, che include uno scheletro di flavanone, contribuendo alle sue potenziali attività biologiche. Questo composto presenta varie proprietà farmacologiche, inclusi effetti anti-infiammatori, antiossidanti e anticancerogeni, rendendolo di interesse nella chimica medicinale e nella ricerca di prodotti naturali. Sophoraflavanone G si trova tipicamente sotto forma di solido cristallino giallastro ed è solubile in solventi organici. La sua formula molecolare riflette la presenza di più gruppi idrossilici, responsabili della sua reattività e interazione con i sistemi biologici. La ricerca su Sophoraflavanone G continua a esplorare i suoi meccanismi d'azione e le potenziali applicazioni terapeutiche, in particolare nel contesto di malattie croniche e condizioni correlate allo stress ossidativo. Come molti flavonoidi, la sua biodisponibilità e le vie metaboliche sono anche oggetto di indagine continua, evidenziando la complessità dei suoi effetti in vivo.

Formula: 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

InChI key: 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

Sinonimi:

• (-)-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

Formula: C₂₅H₂₈O₆

Purezza: 99.5%

Peso molecolare: 424.49

Ref: 54-BUP08940

Kushenol F

CAS: 97938-30-2

Formula: C₂₅H₂₈O₆

Purezza: 95%~99%

Peso molecolare: 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.

Formula: C₂₅H₂₈O₆

Peso molecolare: 424.49

Ref: TM-TMSM-1920

Sophoraflavanone G

CAS: 97938-30-2

Formula: C₂₅H₂₈O₆

Purezza: 99%

Colore e forma: Solid

Peso molecolare: 424.4862

Ref: IN-DA005XAK

Sophoraflavanone G

CAS: 97938-30-2

Formula: C₂₅H₂₈O₆

Purezza: ≥ 98.0%

Colore e forma: White to off-white powder

Peso molecolare: 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

Formula: C₂₅H₂₈O₆

Purezza: 97.09% - 99.77%

Colore e forma: Solid

Peso molecolare: 424.4862

Ref: TM-T5S1000

Sophoraflavanone G

CAS: 97938-30-2

Oxygen-heterocyclic compound

Formula: C₂₅H₂₈O₆

Purezza: ≥ 95.0 % (HPLC)

Colore e forma: Powder

Peso molecolare: 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.

Formula: C₂₅H₂₈O₆

Purezza: Min. 95%

Colore e forma: White Powder

Peso molecolare: 424.49 g/mol

Ref: 3D-FN74220

Sophoraflavanone G

CAS: 97938-30-2

Formula: C₂₅H₂₈O₆

Peso molecolare: 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

Formula: C₂₅H₂₈O₆

Purezza: 99%

Peso molecolare: 424.49

Ref: IN-DG298349