product summary
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company name :
Tocris Bioscience
product type :
chemical
product name :
RP 67580
catalog :
1635/10
quantity :
10 mg (also 50 mg)
price :
292 USD
more info or order :
citations: 6
Reference
Jeong Y, Cheng X, Kim W. Substance P Administered after Myocardial Infarction Upregulates Microphthalmia-Associated Transcription Factor, GATA4, and the Expansion of c-Kit+ Cells. Stem Cells Int. 2020;2020:1835950 pubmed publisher
Wang G, Wang X, Liu S, Qu M, Xia Y, Needleman B, et al. Innervation of enteric mast cells by primary spinal afferents in guinea pig and human small intestine. Am J Physiol Gastrointest Liver Physiol. 2014;307:G719-31 pubmed publisher
Chai B, Guo W, Wei F, Dubner R, Ren K. Trigeminal-rostral ventromedial medulla circuitry is involved in orofacial hyperalgesia contralateral to tissue injury. Mol Pain. 2012;8:78 pubmed publisher
Russell F, Schuelert N, Veldhoen V, Hollenberg M, McDougall J. Activation of PAR(2) receptors sensitizes primary afferents and causes leukocyte rolling and adherence in the rat knee joint. Br J Pharmacol. 2012;167:1665-78 pubmed publisher
Zhong B, Wang D. Protease-activated receptor 2-mediated protection of myocardial ischemia-reperfusion injury: role of transient receptor potential vanilloid receptors. Am J Physiol Regul Integr Comp Physiol. 2009;297:R1681-90 pubmed publisher
Wang Y, Novotny M, Quaiserová Mocko V, Swain G, Wang D. TRPV1-mediated protection against endotoxin-induced hypotension and mortality in rats. Am J Physiol Regul Integr Comp Physiol. 2008;294:R1517-23 pubmed publisher
product information
brand :
Tocris, a Bio-Techne brand
catalog number base :
1635
SKU :
1635/10
product name :
RP 67580
description :
Potent and selective NK1 antagonist
target :
NK1 Receptor Antagonists
unit size :
10 mg (also 50 mg)
category :
Small Molecules
purity :
97%
storage :
Store at -20°C
observed molecular weight :
438.57
url print :
?utm_source=biocompare&utm_medium=referral&utm_campaign=product&utm_term=smallmolecules
details of functionality :
RP 67580 is a potent and selective tachykinin NK1 receptor antagonist (Ki values are 2.9 nM and 10 u M for rat NK1, and rat NK2 and NK3 receptors respectively). Displays higher affinity at rat and mouse than human receptors. Antinociceptive in vivo , possibly partly via inhibition of calcium channels.
product keywords :
Potent selective NK1 antagonists Tachykinin Receptors Neurokinin RP67580 NK1 Receptor 1635, Neurokinin NK1
extended description :
Potent and selective NK1 antagonist
chemical name text :
(3aR,7aR)-Octahydro-2-[1-imino-2-(2-methoxyphenyl)ethyl]-7,7-diphenyl-4H-isoindol
formula :
C29H30N2O2
formula text :
C29H30N2O2
cas num :
135911-02-3
USD :
289
USD 2025 :
292 USD
product details :
Potent and selective NK1 antagonist
more info or order :
company information
Tocris Bioscience
The Watkins Building
Atlantic Road
Avonmouth, Bristol
BS11 9QD
info@bio-techne.com
https://www.tocris.com
800-343-7475
headquarters: UK