Oxyphyllenodiol B

Catalog No.: B18593
Sesquiterpene
Oxyphyllenodiol B is an eremophilane-type sesquiterpene extracted from the fruits of Alpinia oxyphylla. This compound demonstrates potential anti-inflammatory activity through the inhibition of nitric oxide (NO) production, making it a valuable reagent for studies focused on inflammation pathways. Additionally, research into Alpinia oxyphylla has revealed its traditional use in addressing conditions such as diarrhea and dementia, indicating potential therapeutic applications for Oxyphyllenodiol B in neuroprotective and gastrointestinal studies.
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5mg
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50mg
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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
DescriptionOxyphyllenodiol B is an eremophilane-type sesquiterpene extracted from the fruits of Alpinia oxyphylla. This compound demonstrates potential anti-inflammatory activity through the inhibition of nitric oxide (NO) production, making it a valuable reagent for studies focused on inflammation pathways. Additionally, research into Alpinia oxyphylla has revealed its traditional use in addressing conditions such as diarrhea and dementia, indicating potential therapeutic applications for Oxyphyllenodiol B in neuroprotective and gastrointestinal studies.
Product Information
Catalog NumB18593
FormulaC14H22O3
Molecular Weight238.32
CAS Number363610-32-6
SMILESCC([C@@H]1C2=C(CC[C@@](O)([C@H]2O)C)C(CC1)=O)C
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