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BIBP3226

Chemical Structure : BIBP3226

CAS No.: 159013-54-4

BIBP3226 (BIBP 3226, BIBP-3226)

Catalog No.: PC-27938Not For Human Use, Lab Use Only.

BIBP3226 (BIBP 3226) is a highly potent and selective non-peptide neuropeptide Y Y1 receptor (NPY1R) antagonist with Ki of 7 nM.

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

Biological Activity

BIBP3226 (BIBP 3226) is a highly potent and selective non-peptide neuropeptide Y Y1 receptor (NPY1R) antagonist with Ki of 7 nM.
BIBP3226 potently blocks (pA2 = 7.36) the contractile effect of neuropeptide Y in the rabbit saphenous vein, a Y1 receptor bioassay and demonstrated nM affinity for Y1/[125I][Leu31,Pro34]peptide YY binding sites.
BIBP3226 (BIBP 3226) does not significantly compete for Y2/[125I]peptide YY-(3-36) binding sites in rat and human brain homogenates.
BIBP3226 (BIBP 3226) antagonizes the NPY Y1 receptor-mediated decrease in the twitch response in the rabbit vas deferens preparation with a pKb value of 6.98.
BIBP3226 (BIBP 3226) inhibits NPY-induced increase in blood pressure in the pithed rat.

Physicochemical Properties

M.Wt 473.58
Formula C27H31N5O3
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

(R)-2-(2,2-Diphenylacetamido)-5-guanidino-N-(4-hydroxybenzyl)pentanamide

References

1. Jacques D, et al. Eur J Pharmacol. 1995 May 4;278(1):R3-5.

2. Rudolf K, et al. Eur J Pharmacol. 1994 Dec 27;271(2-3):R11-3.

3. Mollereau C, et al. Br J Pharmacol. 2001 May;133(1):1-4.

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