Lacidipine-13C8

Catalog No.: A25103
Stable Isotope
Lacidipine-13C8 is a deuterium-labeled derivative of Lacidipine, a highly selective L-type calcium channel blocker that primarily targets smooth muscle cells. This compound is known for its ability to dilate peripheral arteries, thereby reducing peripheral resistance and providing sustained antihypertensive effects. Lacidipine has also demonstrated protective effects on human kidney cells by modulating the caspase-3 pathway in response to ATP depletion. It is applicable in research related to hypertension, atherosclerosis, and acute kidney injury (AKI).
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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
DescriptionLacidipine-13C8 is a deuterium-labeled derivative of Lacidipine, a highly selective L-type calcium channel blocker that primarily targets smooth muscle cells. This compound is known for its ability to dilate peripheral arteries, thereby reducing peripheral resistance and providing sustained antihypertensive effects. Lacidipine has also demonstrated protective effects on human kidney cells by modulating the caspase-3 pathway in response to ATP depletion. It is applicable in research related to hypertension, atherosclerosis, and acute kidney injury (AKI).
Product Information
Catalog NumA25103
FormulaC1813C8H33NO6
Molecular Weight463.48
CAS Number1261432-01-2
SMILESCCO[13C]([13C]1=[13C](N[13C]([13CH3])=[13C](C1C2=C(/C=C/C(OC(C)(C)C)=O)C=CC=C2)[13C](OCC)=O)[13CH3])=O
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