CAS 131573-90-5: camelliaside B
Description:Camelliaside B is a chemical compound primarily derived from the Camellia genus, particularly from plants like Camellia sinensis (tea plant). It is classified as a triterpenoid saponin, which is characterized by its complex structure that includes a steroid-like backbone and sugar moieties. This compound exhibits various biological activities, including antioxidant, anti-inflammatory, and potential anticancer properties, making it of interest in pharmacological research. Camelliaside B is soluble in polar solvents, which is typical for saponins, and its structure allows it to interact with biological membranes, potentially influencing cell signaling pathways. The compound's unique properties are attributed to its specific arrangement of functional groups, which contribute to its reactivity and biological efficacy. As research continues, the full range of its applications and mechanisms of action is being explored, highlighting its significance in both traditional medicine and modern therapeutic contexts.
Formula:C32H38O19
InChI:InChI=1S/C32H38O19/c1-10-19(37)23(41)26(44)30(47-10)46-9-17-21(39)24(42)29(51-31-25(43)20(38)15(36)8-45-31)32(49-17)50-28-22(40)18-14(35)6-13(34)7-16(18)48-27(28)11-2-4-12(33)5-3-11/h2-7,10,15,17,19-21,23-26,29-39,41-44H,8-9H2,1H3/t10-,15+,17+,19-,20-,21+,23+,24-,25+,26+,29+,30+,31-,32-/m0/s1
InChI key:InChIKey=LLPRITPJQPQXIR-BVDHFOMSSA-N
SMILES:O=C1C(OC2OC(COC3OC(C)C(O)C(O)C3O)C(O)C(O)C2OC4OCC(O)C(O)C4O)=C(OC=5C=C(O)C=C(O)C15)C=6C=CC(O)=CC6
- Synonyms:
- 3-[(O-6-Deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→6)-O-[β-<smallcap>D</smallcap>-xylopyranosyl-(1→2)]-β-<smallcap>D</span>-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 4H-1-Benzopyran-4-one, 3-((O-6-deoxy-alpha-L-mannopyranosyl-(1-6)-O-(beta-D-xylopyranosyl-(1-2))-beta-D-glucopyranosyl)oxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 4H-1-Benzopyran-4-one, 3-[(O-6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→6)-O-[β-<smallcap>D</smallcap>-xylopyranosyl-(1→2)]-β-<smallcap>D</span>-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-
- 5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->3)-[beta-D-xylopyranosyl-(1->2)]-alpha-D-glucopyranoside
- Kaempferol 3-(2<sup>G</sup>-xylosylrutinoside)
- Kaempferol 3-O-(2<sup>G</sup>-β-<span class="text-smallcaps">D</span>-xylopyranosylrutinoside)
- Kampferol 3-O-(2-O-xylopyranosyl-6-O-rhamnopyranosyl)glucopyranoside
- k-Xyl-rha-glu
- 3-[(O-6-Deoxy-α-L-mannopyranosyl-(1→6)-O-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- Camelliaside B
- See more synonyms
- Kaempferol 3-(2G-xylosylrutinoside)
- Kaempferol 3-O-(2G-β-D-xylopyranosylrutinoside)
- 4H-1-Benzopyran-4-one, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→6)-O-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-
