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Adrenomedullin (1-52) (human) (trifluoroacetate salt)

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    Adrenomedullin (1-52) (human) (trifluoro<wbr/>acetate salt)
  • Adrenomedullin (1-52) (human) (trifluoro<wbr/>acetate salt)
Cat No: 24889
Biochemicals - Peptides
Cayman

Adrenomedullin (1-52) is a peptide with diverse biological activities.{39625,39626,39627,39628} It belongs to the calcitonin family of peptides, which includes amylin (Item Nos. 24274
24275), calcitonin gene-related peptide (Item Nos. 24405
24725 ...

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: 500 µg

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • adrenomedullin (human), trifluoroacetate salt
Correlated keywords:
  • 148498-78-6 U46619
Product Overview:
Adrenomedullin (1-52) is a peptide with diverse biological activities.{39625,39626,39627,39628} It belongs to the calcitonin family of peptides, which includes amylin (Item Nos. 24274
24275), calcitonin gene-related peptide (Item Nos. 24405
24725
24728), and calcitonin (Item Nos. 24409
24410).{39625} Adrenomedullin (1-52) is expressed in pheochromocytomas, adrenal medulla, heart, lung, and kidney as well as human umbilical vein endothelial cells (HUVECs) and in human glomerular epithelial and hematopoietic cell lines. In vivo, adrenomedullin (1-52) (10-3,000 ng per animal) reverses increases in lobar arterial pressure induced by U-46619 (Item No. 16450) in a dose-dependent manner in cats but has no effect on basal lobar arterial pressure or systemic arterial pressure.{39626} It reduces mechanical ventilation-induced lung injury and sepsis as well as liver and gut injury induced by ventilator-induced lung injury in a mouse model of pneumococcal pneumonia infection.{39627} Adrenomedullin (1-52) improves survival and inhibits cardiac tissue damage induced by doxorubicin (Item No. 15007) in mice.{39628} Adrenomedullin (1-52) also reduces hyperoxia-induced right ventricular hypertrophy and artery thickness in a rat model of bronchopulmonary dysplasia.{39625}
Size 500 µg
Shipping dry ice
Molecular Formula C264H406N80O77S3 • XCF3COOH
SMILES NC([C@@H](NC(CNC([C@H](CCC(N)=O)NC([C@@H]1CCCN1C([C@H](CO)NC([C@@]([C@H](CC)C)([H])NC([C@H](CCCCN)NC([C@H](CO)NC([C@H](CCCNC(N)=N)NC([C@@H]2CCCN2C([C@@H](NC([C@H](C(C)C)NC([C@H](CC(N)=O)NC([C@@H](NC([C@H](CCCCN)NC([C@@H](NC([C@H](CCCCN)NC([C@@H](NC([C@@](
Molecular Weight 6028,7
Formulation A lyophilized powder
Purity ≥95%
Custom Code 3504.00
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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