Amlodipine mesylate

Catalog No.: A66139
Calcium Channel Blocker
Amlodipine mesylate is a potent dihydropyridine calcium channel blocker that inhibits voltage-dependent L-type calcium channels, leading to decreased calcium influx. This mechanism results in vasodilation and reduced cardiac workload, making it an important agent in the study of hypertension and ischemic heart disease. Amlodipine mesylate is also being explored for its potential applications in cancer research due to its effects on vascular dynamics.
Grouped product items
Size Price Stock Qty
25mg
$1,800.00
In stock
50mg
$2,285.00
In stock
100mg
$2,815.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
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
DescriptionAmlodipine mesylate is a potent dihydropyridine calcium channel blocker that inhibits voltage-dependent L-type calcium channels, leading to decreased calcium influx. This mechanism results in vasodilation and reduced cardiac workload, making it an important agent in the study of hypertension and ischemic heart disease. Amlodipine mesylate is also being explored for its potential applications in cancer research due to its effects on vascular dynamics.
Product Information
Catalog NumA66139
FormulaC21H29ClN2O8S
Molecular Weight504.98
CAS Number246852-12-0
SMILESO=S(C)(O)=O.O=C(C1=C(COCCN)NC(C)=C(C(OC)=O)C1C2=CC=CC=C2Cl)OCC
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