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[Pro9] Substance P (CAS 104486-69-3)

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Alternate Names:
[Pro9]-Substance P
Application:
[Pro9] Substance P is a selective NK1 agonist
CAS Number:
104486-69-3
Molecular Weight:
1387.73
Molecular Formula:
C66H102N18O13S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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[Pro9] Substance P is a synthetic analog of the neuropeptide Substance P, engineered by substituting the ninth amino acid with proline to enhance its stability and modify its interaction with neurokinin-1 (NK1) receptors. This chemical is primarily used in research to probe the dynamics of pain perception and neurogenic inflammation. The mechanism of action for [Pro9] Substance P involves binding to NK1 receptors, which are G protein-coupled receptors predominantly found in the nervous system. Upon activation, these receptors stimulate signaling pathways that include the activation of phospholipase C, leading to increased production of inositol triphosphate and diacylglycerol. This cascade elevates intracellular calcium levels, which facilitates various physiological responses, including neuronal excitation and neurotransmitter release. In scientific studies, [Pro9] Substance P has been a valuable tool for investigating the role of NK1 receptors in pain pathways and inflammatory responses, helping to unravel complex neurochemical interactions and contributing to our understanding of neurotransmission without being directly linked to therapeutic applications. This peptide has thus been instrumental in advancing knowledge about receptor pharmacology and the modulation of inflammatory processes in the nervous system.


[Pro,[object Object],] Substance P (CAS 104486-69-3) References

  1. Further demonstration that [Pro9]-substance P is a potent and selective ligand of NK-1 tachykinin receptors.  |  Petitet, F., et al. 1991. J Neurochem. 56: 879-89. PMID: 1704425
  2. Comparison of the effects of epithelium removal and of an enkephalinase inhibitor on the neurokinin-induced contractions of guinea-pig isolated trachea.  |  Devillier, P., et al. 1988. Br J Pharmacol. 94: 675-84. PMID: 2460177
  3. Tachykinin NK1 receptors mediate both vasoconstrictor and vasodilator responses in the rabbit isolated jugular vein.  |  Patacchini, R. and Maggi, CA. 1995. Eur J Pharmacol. 283: 233-40. PMID: 7498315
  4. Intranigral stimulation of oral movements by [Pro9] substance P, a neurokinin-1 receptor agonist, is enhanced in chronically neuroleptic-treated rats.  |  Liminga, U. and Gunne, LM. 1993. Behav Brain Res. 57: 93-9. PMID: 7507330
  5. Highly potent substance P antagonists substituted with beta-phenyl- or beta-benzyl-proline at position 10.  |  Lavielle, S., et al. 1994. Eur J Pharmacol. 258: 273-6. PMID: 7522179
  6. Typical and atypical NK1 tachykinin receptor characteristics in the rabbit isolated iris sphincter.  |  Hall, JM., et al. 1994. Br J Pharmacol. 112: 985-91. PMID: 7522864
  7. Higher potency of RP 67580, in the mouse and the rat compared with other nonpeptide and peptide tachykinin NK1 antagonists.  |  Beaujouan, JC., et al. 1993. Br J Pharmacol. 108: 793-800. PMID: 7682138
  8. Interaction of the substance P receptor antagonist RP 67580 with the rat brain NK1 receptor expressed in transfected CHO cells.  |  Hermans, E., et al. 1993. Eur J Pharmacol. 245: 43-50. PMID: 7682962
  9. Comparative behavioural profile of centrally administered tachykinin NK1, NK2 and NK3 receptor agonists in the guinea-pig.  |  Piot, O., et al. 1995. Br J Pharmacol. 116: 2496-502. PMID: 8581290
  10. Distinct regulations by septide and the neurokinin-1 tachykinin receptor agonist [pro9]substance P of the N-methyl-D-aspartate-evoked release of dopamine in striosome- and matrix-enriched areas of the rat striatum.  |  Gauchy, C., et al. 1996. Neuroscience. 73: 929-39. PMID: 8809812

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

[Pro9] Substance P, 500 µg

sc-396074
500 µg
$75.00

[Pro9] Substance P, 2.5 mg

sc-396074A
2.5 mg
$188.00