Ethyl-3,5-di-O-caffeoylquinate

Catalog No.: A36349
Ethyl Caffeoylquinate
Ethyl-3,5-di-O-caffeoylquinate is a derivative of ethyl caffeoylquinate, primarily targeting α-glucosidase and PTP1B enzymes. This compound demonstrates potential as an inhibitor of these critical enzymes, making it valuable for research in metabolic disorders and diabetes management. Isolated from the flower buds of Lonicera macranthoides, it also serves as an isomer of chlorogenic acid (ethyl dicaffeoylquinate), expanding its relevance in phytochemical studies and pharmacological applications.
Grouped product items
Size Price Stock Qty
5mg
$375.00
In stock
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Research use only. We do not sell to patients.

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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
DescriptionEthyl-3,5-di-O-caffeoylquinate is a derivative of ethyl caffeoylquinate, primarily targeting α-glucosidase and PTP1B enzymes. This compound demonstrates potential as an inhibitor of these critical enzymes, making it valuable for research in metabolic disorders and diabetes management. Isolated from the flower buds of Lonicera macranthoides, it also serves as an isomer of chlorogenic acid (ethyl dicaffeoylquinate), expanding its relevance in phytochemical studies and pharmacological applications.
Product Information
Catalog NumA36349
FormulaC27H28O12
Molecular Weight544.50
CAS Number143051-74-5
SMILESCCOC([C@]1(C[C@H]([C@@H]([C@@H](C1)OC(/C=C/C2=CC(O)=C(C=C2)O)=O)O)OC(/C=C/C3=CC(O)=C(C=C3)O)=O)O)=O
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