CAS 168037-22-7

[3,4′-Bibenzofurano]-6,6′-diolo, 3′-(3,5-diidrossifenile)-2,2′,3,3′-tetraidro-2,2′-bis(4-idrossifenile)-4-[(1Z)-2-(4-idrossifenile)etenile]-, (2S,2′R,3S,3′R)-

Descrizione:

La sostanza chimica nota come [3,4′-Bibenzofurano]-6,6′-diolo, 3′-(3,5-diidrossifenile)-2,2′,3,3′-tetraidro-2,2′-bis(4-idrossifenile)-4-[(1Z)-2-(4-idrossifenile)etenile]-, (2S,2′R,3S,3′R)-, con numero CAS 168037-22-7, è un composto organico complesso caratterizzato dalla sua struttura polifenolica. Questo composto presenta più gruppi idrossilici, che contribuiscono alle sue potenziali proprietà antiossidanti e reattività in vari ambienti chimici. La presenza di più anelli aromatici suggerisce che potrebbe mostrare una stabilità significativa e caratteristiche idrofobiche, mentre la stereochimica indicata dalla sua configurazione (2S,2′R,3S,3′R) implica disposizioni spaziali specifiche che potrebbero influenzare la sua attività biologica e interazioni. Tali composti sono spesso di interesse nella chimica medicinale e nella scienza dei materiali a causa delle loro potenziali applicazioni nello sviluppo di farmaci e come materiali funzionali. Inoltre, la struttura intricata può consentire varie interazioni intermolecolari, rendendolo un candidato per ulteriori ricerche in campi come biochimica e farmacologia.

Formula: C₄₂H₃₂O₉

InChI: InChI=1S/C42H32O9/c43-27-9-2-22(3-10-27)1-4-25-15-32(48)20-35-37(25)40(42(50-35)24-7-13-29(45)14-8-24)34-19-33(49)21-36-39(34)38(26-16-30(46)18-31(47)17-26)41(51-36)23-5-11-28(44)12-6-23/h1-21,38,40-49H/b4-1-/t38-,40+,41+,42-/m1/s1

InChI key: InChIKey=RKFYYCKIHVEWHX-LXJGKARHSA-N

SMILES: C(=C\C1=CC=C(O)C=C1)\C2=C3[C@@H]([C@H](OC3=CC(O)=C2)C4=CC=C(O)C=C4)C5=C6[C@H]([C@@H](OC6=CC(O)=C5)C7=CC=C(O)C=C7)C8=CC(O)=CC(O)=C8

Sinonimi:

• [3,4′-Bibenzofuran]-6,6′-diol, 3′-(3,5-dihydroxyphenyl)-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-, [2S-[2α,3β(2′S*,3′S*),4(Z)]]-
• cis-Miyabenol C
• [3,4′-Bibenzofuran]-6,6′-diol, 3′-(3,5-dihydroxyphenyl)-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-, (2S,2′R,3S,3′R)-
• (2S,2'R,3S,3'R)-3'-(3,5-Dihydroxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-[3,4'-bibenzofuran]-6,6'-diol
• [3,4'-Bibenzofuran]-6,6'-diol,3'-(3,5-dihydroxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-, (2S,2'R,3S,3'R)-
• [3,4'-Bibenzofuran]-6,6'-diol, 3'-(3,5-dihydroxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-, (2S,2'R,3S,3'R)- (9CI)

cis-Miyabenol C

CAS: 168037-22-7

Formula: C₄₂H₃₂O₉

Purezza: 93.0%

Peso molecolare: 680.6981

Ref: IN-DA00ASII

cis-Miyabenol C

CAS: 168037-22-7

cis-Miyabenol C exhibits antioxidative activities and shows strong hyaluronidase inhibitory effects. cis-Miyabenol C also has ecdysteroid antagonist activity.

Formula: C₄₂H₃₂O₉

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 680.709

Ref: TM-TN3668

Cis-miyabenol C

CAS: 168037-22-7

Cis-miyabenol C is a type of polyphenolic compound, which is a resveratrol tetramer found naturally in certain plant species, including grapevines and the roots of the plant Gnetum cleistostachyum. As a naturally occurring stilbene derivative, it is biosynthesized as part of the plant's defense mechanism against pathogens. Its mode of action is believed to involve modulation of various signaling pathways and antioxidant properties. Studies suggest that it can influence cellular processes by binding to specific proteins and enzymes, thereby altering their activity.

Formula: C₄₂H₃₂O₉

Purezza: Min. 95%

Peso molecolare: 680.70 g/mol

Ref: 3D-TGA03722