Biological Activity for Substance P

Substance p is a sensory neuropeptide và inflammatory mediator. Exerts excitatory effects on central & peripheral neurons, constricts bronchioles and is involved in pain transmission.

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Technical Data for Substance P

M. Wt 1347.6
Formula C63H98N18O13S

(Modifications: Met-11 = C-terminal amide)

Storage Store at -20°C
Purity ≥95% (HPLC)
CAS Number 33507-63-0
PubChem ID 36511
Smiles NH>(CCSC)C(N)=O

The technical data provided above is for guidance only. For batch specific data refer to lớn the Certificate of Analysis. products are intended for laboratory research use only, unless stated otherwise.

References for Substance P

References are publications that support the biological activity of the product.

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Andoh et al (1998) Substance p. Induction of itch-associated response mediated by cutaneous NK1 tachykinin receptors in mice. J.Pharmacol.Exp.Ther. 286 1140 PMID:9732370 Pernow et al (1983) Substance p Pharmacol.Rev. 35 85 PMID:6196797 Walsh et al (1995) Substance P-induced inflammatory responses in guinea-pig skin: the effect of specific NK1 receptor antagonists and the role of endogenous mediators. Br.J.Pharmacol. 114 1343 PMID:7541689 Merck Index 12 9032 If you know of a relevant reference for Substance P, please let us know.

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Keywords: Substance P, Substance p. Supplier, Sensory, neuropeptide, inflammatory, mediators, Tachykinin, Non-Selective, Neurokinin, Receptors, agonists, SubstanceP, neuropeptides, Other, 1156, Bioscience

15 Citations for Substance P

Citations are publications that use products. Selected citations for Substance phường include:

Wease & Davies (2005) Substance phường selectively decreases paired pulse depression in the rat hippocampal slice. BMC Neurosci 6 66 PMID:16305744

Alsaqati et al (2013) Investigation of the functional expression of purine and pyrimidine receptors in porcine isolated pancreatic arteries. Purinergic Signal 10 241 PMID:24310605

Howe et al (2004) Role of neurokinin 3 receptors in supraoptic vasopressin và oxyt. Neurons. J Biomol Screen 24 10103 PMID:15537880

Gutierrez and Boada (2019) Neuropeptide-induced modulation of carcinogenesis in a metastatic breast cancer cell line (MDA-MB-231LUC+). Cancer Cell Int 18 216 PMID:30598641

Nogueras-Ortiz (2017) Retromer stops beta-arrestin 1 mediated signaling from internalized cannabinoid 2 receptors. Mol Biol Cell 28 3554 PMID:28954865

Hur & Park (2013) Long-term potentiation of excitatory synaptic strength in spinothalamic tract neurons of the rat spinal cord. Korean J Physiol Pharmacol 17 553 PMID:24381506

Hanson et al (2009) A homogeneous fluorescent live-cell assay for measuring 7-transmembrane receptor activity and agonist functional selectivity through β-arrestin recruitment. Antioxid Redox Signal 14 798 PMID:19531663

Li et al (2009) Activation of glycogen synthase kinase-3 β is required for hyperDA và D2 receptor-mediated inhibition of synaptic NMDA receptor function in the rat prefrontal cortex. J Neurosci 29 15551 PMID:20007479

Wan et al (2017) Endomorphin-2 Inhibition of Substance p. Signaling within Lamina I of the Spinal Cord Is Impaired in Diabetic Neuropathic Pain Rats. Front Mol Neurosci 9 167 PMID:28119567

Fisher et al (2015) Increased CCN2, substance phường and tissue fibrosis are associated with sensorimotor declines in a rat model of repetitive overuse injury. J Cell Commun Signal 9 37 PMID:25617052

Robery et al (2011) Investigating the effect of emetic compounds on chemotaxis in Dictyostelium identifies a non-sentient model for bitter and hot tastant research. PLoS One 6 e24439 PMID:21931717

Shanley et al (2011) Evidence for regulatory diversity and auto-regulation at the TAC1 locus in sensory neurones. J Neurosci 8 10 PMID:21294877

Kowtharapu et al (2018) Role of Corneal Stromal Cells on Epithelial Cell Function during Wound Healing. Int J Mol Sci 19 PMID:29401709

Frara et al (2018) Substance p. Increases CCN2 dependent on TGF-beta yet Collagen Type I via TGF-beta1 dependent & independent pathways in tenocytes. Connect Tissue Res 59 30 PMID:28399671

Chen et al (2014) μ-Opioid receptor inhibition of substance p release from primary afferents disappears in neuropathic pain but not inflammatory pain. Neuroscience 267 67 PMID:24583035