Otophylloside Q

Catalog No.: A95614
Glycoside
Otophylloside Q is a pregnane glycoside targeting glycoside receptors, extracted from the roots of Cynanchum otophyllum. This compound features caudatin as its aglycone, which is known for its potential anticancer properties. Otophylloside Q's complex sugar chain comprises cymarose, oleandrose, and glucose units, making it a subject of interest for studies involving cancer research and the modulation of glycoside activity in biological systems.
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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionOtophylloside Q is a pregnane glycoside targeting glycoside receptors, extracted from the roots of Cynanchum otophyllum. This compound features caudatin as its aglycone, which is known for its potential anticancer properties. Otophylloside Q's complex sugar chain comprises cymarose, oleandrose, and glucose units, making it a subject of interest for studies involving cancer research and the modulation of glycoside activity in biological systems.
Product Information
Catalog NumA95614
FormulaC68H110O29
Molecular Weight1391.58
CAS Number1326583-13-4
SMILESO[C@]12[C@@]3([C@]([C@@H](C[C@]1([H])[C@@]4(C(C[C@H](CC4)O[C@H]5C[C@@H]([C@@H]([C@H](O5)C)O[C@H]6C[C@@H]([C@@H]([C@H](O6)C)O[C@H]7C[C@H]([C@@H]([C@H](O7)C)O[C@H]8C[C@@H]([C@@H]([C@H](O8)C)O[C@@H]9O[C@@H]([C@H]([C@@H]([C@H]9O)O)O[C@@H]%10O[C@@H]([C@H]([C@@H]([C@H]%10O)O)O)CO)CO)OC)OC)OC)OC)=CC2)C)OC(/C=C(C)/C(C)C)=O)([C@@](O)(CC3)C(C)=O)C)O
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