CAS 168037-22-7

[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)-

Description:

The chemical substance known as [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)-, with CAS number 168037-22-7, is a complex organic compound characterized by its polyphenolic structure. This compound features multiple hydroxyl groups, which contribute to its potential antioxidant properties and reactivity in various chemical environments. The presence of multiple aromatic rings suggests that it may exhibit significant stability and hydrophobic characteristics, while the stereochemistry indicated by its (2S,2′R,3S,3′R)- configuration implies specific spatial arrangements that could influence its biological activity and interactions. Such compounds are often of interest in medicinal chemistry and materials science due to their potential applications in drug development and as functional materials. Additionally, the intricate structure may allow for various intermolecular interactions, making it a candidate for further research in fields such as biochemistry and pharmacology.

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

Synonyms:

• [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

Purity: 93.0%

Molecular weight: 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

Purity: 98%

Color and Shape: Solid

Molecular weight: 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

Purity: Min. 95%

Molecular weight: 680.70 g/mol

Ref: 3D-TGA03722