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A71623

Chemical Structure : A71623

CAS No.: 130408-77-4

A71623 (A-71623)

Catalog No.: PC-22020Not For Human Use, Lab Use Only.

A-71623 (A71623) is a cholecystokinin tetrapeptide (30-33) analogue as potent, highly selective CCK-A (CCK1) cholecystokinin receptor agonist with binding IC50 of 3.7 nM, >1000-fold selective over CCK-B receptor.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

A-71623 (A71623) is a cholecystokinin tetrapeptide (30-33) analogue as potent, highly selective CCK-A (CCK1) cholecystokinin receptor agonist with binding IC50 of 3.7 nM, >1000-fold selective over CCK-B receptor.
A-71623 exhibits IC50 values for A-71623 and A-70874 were 3.7 and 4.9 nM in guinea pig pancreas (CCK-A) and 4500 and 710 nM in cerebral cortex (CCK-B), respectively, in radioligand binding assays.
In daily injection studies, the anorectic activity of CCK-8 diminished rapidly, whereas the suppressant effects of A71623 on food intakes and body weight gains persisted throughout the 11-day treatment period.
A71623 reduced the spontaneous locomotor activity of rats at doses above those required to suppress intakes.

Physicochemical Properties

M.Wt 840.98
Formula C44H56N8O9
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-[(1,1-Dimethylethoxy)carbonyl]-L-tryptophyl-N6-[[(2-methylphenyl)amino]carbonyl]-L-lysyl-L-α-aspartyl-Nα-methyl-L-phenylalaninamide

References

1. Lin CW, et al. Mol Pharmacol. 1991 Mar;39(3):346-51.

2. Asin KE, et al. Am J Physiol. 1992 Jul;263(1 Pt 2):R125-35.

3. Asin KE, et al. Pharmacol Biochem Behav. 1992 Aug;42(4):699-704.

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