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[Pro9]-Substance P

Cat. No. Size Price Figures
RP10208-0.5 mg
 		0.5 mg
$ 24.00
HPLC:  20060721145614  (PDF)
MS:  20060721145554  (PDF)
MSDS:  20080626230832  (PDF)
PROTOCOL:  20100407015038  (PDF)

STRUCTURE:
[Pro<sup>9</sup>]-Substance P Structure
Zoom

References:
  • Kawana S, et al. Role of substance P in stress-derived degranulation of dermal mast cells in mice. J. Dermatol. Sci. Apr 2006; 42(1): 47-54.
  • Seybold VS, et al. Substance P initiates NFAT-dependent gene expression in spinal neurons. J. Neurochem. Apr 2006; 97(2): 397-407.
Full Name
[Pro9]-Substance P
Alias [Pro9]-SP
Sequence
(one-letter code)		 RPKPQQFFPLM-NH2
Sequence
(three-letter code)		{ARG}{PRO}{LYS}{PRO}{GLN}{GLN}{PHE}{PHE}{PRO}{LEU}
{MET}-NH2
C-TerminalNH2
Description[Pro9]-substance P ([Pro9]-SP) possesses has very good affinity for NK-1 binding sites and that, in contrast to substance P, it interacts selectively with these sites. [Pro9]-SP had neither agonist nor antagonist properties on NK-2 and NK-3 receptors. Indeed, it did not stimulate phosphoinositide turnover on the hamster urinary bladder (NK-2 assay) and was devoid of activity on the contraction of the rabbit pulmonary artery (NK-2 assay) and of the rat portal vein (NK-3 assay). As a result of its high selectivity, [Pro9]-SP thus appears an excellent tool for investigating the functional properties of NK-1 receptors.
FormulaC66H102N18O13S
M.W.1387.69
Cas104486-69-3
Purity> 95%
StorageStore at -20°C. Keep tightly closed.
* For Non-Clinical Research Use Only *
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