EM574

Catalog No.: A61951
Motilin Receptor Agonist
EM574 is a potent agonist of the motilin receptor, demonstrating significant activity in the human gastric antrum and rabbit gastrointestinal tract in vitro. As an erythromycin derivative, EM574 is utilized in research applications exploring gastrointestinal motility and related disorders. Its ability to selectively modulate motilin receptor signaling makes it a valuable tool for advancing studies in gastrointestinal physiology and pharmacology.
Grouped product items
Size Price Stock Qty
500µg
$255.00
In stock
1mg
$510.00
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
DescriptionEM574 is a potent agonist of the motilin receptor, demonstrating significant activity in the human gastric antrum and rabbit gastrointestinal tract in vitro. As an erythromycin derivative, EM574 is utilized in research applications exploring gastrointestinal motility and related disorders. Its ability to selectively modulate motilin receptor signaling makes it a valuable tool for advancing studies in gastrointestinal physiology and pharmacology.
Product Information
Catalog NumA61951
FormulaC39H69NO12
Molecular Weight743.96
CAS Number110480-13-2
SMILESC[C@@](OC([C@@H]([C@H]([C@](O)1C)O)C)=C2C)(C2)[C@@H]([C@H]([C@@H]([C@H](C(O[C@@H]1CC)=O)C)O[C@H](O[C@H]3C)C[C@](C)([C@H]3O)OC)C)O[C@H](O[C@@H]4C)[C@@H]([C@H](C4)N(C)C(C)C)O
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