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CAS 168010-13-7

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β-D-Glucopyranoside, (2S,2′R,3S,3′R)-3′-[3-(β-D-glucopyranosyloxy)-5-hydroxyphenyl]-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl][3,4′-bibenzofuran]-6,6′-diyl bis-

Description:
The chemical substance known as β-D-Glucopyranoside, with the CAS number 168010-13-7, is a complex glycoside characterized by its structural features, which include multiple phenolic groups and a glucopyranoside moiety. This compound exhibits a high degree of stereochemistry, indicated by its specific configuration at several chiral centers, which contributes to its biological activity and solubility properties. The presence of hydroxyl groups enhances its polarity, making it more soluble in polar solvents, while the phenyl groups may impart hydrophobic characteristics. β-D-Glucopyranoside derivatives are often studied for their potential antioxidant and anti-inflammatory properties, as well as their role in various biochemical pathways. The compound's intricate structure suggests potential interactions with biological macromolecules, which could be relevant in pharmacological applications. Overall, this substance exemplifies the complexity and diversity of glycosides in nature, highlighting their significance in both chemistry and biochemistry.
Formula:C60H62O24
InChI:InChI=1S/C60H62O24/c61-22-40-47(68)50(71)53(74)58(82-40)77-34-17-29(15-33(67)18-34)44-45-37(19-36(79-60-55(76)52(73)49(70)42(24-63)84-60)21-39(45)81-56(44)26-5-11-31(65)12-6-26)46-43-28(4-1-25-2-9-30(64)10-3-25)16-35(78-59-54(75)51(72)48(69)41(23-62)83-59)20-38(43)80-57(46)27-7-13-32(66)14-8-27/h1-21,40-42,44,46-76H,22-24H2
InChI key:InChIKey=OERCOQRGXRNZRU-UHFFFAOYSA-N
SMILES:C(=CC1=CC=C(O)C=C1)C2=C3C(C(OC3=CC(OC4OC(CO)C(O)C(O)C4O)=C2)C5=CC=C(O)C=C5)C6=C7C(C(OC7=CC(OC8OC(CO)C(O)C(O)C8O)=C6)C9=CC=C(O)C=C9)C%10=CC(OC%11OC(CO)C(O)C(O)C%11O)=CC(O)=C%10
Synonyms:
  • Foeniculoside IV
  • b-D-Glucopyranoside, 3'-[3-(b-D-glucopyranosyloxy)-5-hydroxyphenyl]-2,2',3,3'-tetrahydro-2,2'-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl][3,4'-bibenzofuran]-6,6'-diylbis-, [2S-[2a,3b(2'S*,3'S*),4(Z)]]-
  • β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, (2S,2′R,3S,3′R)-3′-[3-(β-<smallcap>D</span>-glucopyranosyloxy)-5-hydroxyphenyl]-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl][3,4′-bibenzofuran]-6,6′-diyl bis-
  • β-<span class="text-smallcaps">D</smallcap>-Glucopyranoside, 3′-[3-(β-<smallcap>D</span>-glucopyranosyloxy)-5-hydroxyphenyl]-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl][3,4′-bibenzofuran]-6,6′-diyl bis-, [2S-[2α,3β(2′S*,3′S*),4(Z)]]-
  • β-D-Glucopyranoside, (2S,2′R,3S,3′R)-3′-[3-(β-D-glucopyranosyloxy)-5-hydroxyphenyl]-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[(1Z)-2-(4-hydroxyphenyl)ethenyl][3,4′-bibenzofuran]-6,6′-diyl bis-
  • β-D-Glucopyranoside, 3′-[3-(β-D-glucopyranosyloxy)-5-hydroxyphenyl]-2,2′,3,3′-tetrahydro-2,2′-bis(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl][3,4′-bibenzofuran]-6,6′-diyl bis-, [2S-[2α,3β(2′S*,3′S*),4(Z)]]-
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