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Submit Review0699 has been discontinued.
The most κ/μ-selective and among the most potent κ ligands known (25 times more potent than morphine in vivo).
Sold with the permission of GlaxoSmithKline
M. Wt | 391.77 |
Formula | C18H24Cl2N2O.HCl |
Storage | Store at RT |
Purity | ≥98% (HPLC) |
CAS Number | 112282-24-3 |
PubChem ID | 11315337 |
InChI Key | NGVLSOWJSUUYDE-UHFFFAOYSA-N |
Smiles | Cl.ClC1=CC=C(CC(=O)N2CCCCC2CN2CCCC2)C=C1Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Vecchietti et al (1991) (2S)-1-(Arylacetyl)-2-(aminomethyl)piperidine derivatives: novel, highly selective κ opioid analgesics. J.Med.Chem. 34 397 PMID: 1846921
Keywords: BRL 52537 hydrochloride, BRL 52537 hydrochloride supplier, Potent, selective, κ-opioid, kappa-opioid, agonist, agonists, KOP, Receptors, OP2, BRL52537, hydrochloride, GlaxoSmithKline, GSK, Kappa, Opioid, 0699, Tocris Bioscience
Citations are publications that use Tocris products. Selected citations for BRL 52537 hydrochloride include:
Morse et al (2013) Label-free integrative pharmacology on-target of opioid ligands at the opioid receptor family. BMC Pharmacol Toxicol 14 17 PMID: 23497702
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
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Written by Sonia Tucci, Lynsay Kobelis and Tim Kirkham, this review provides a synopsis of the increasing number of peptides that have been implicated in appetite regulation and energy homeostasis; putative roles of the major peptides are outlined and compounds available from Tocris are listed.
The key feature of drug addiction is the inability to stop using a drug despite clear evidence of harm. This poster describes the brain circuits associated with addiction, and provides an overview of the main classes of addictive drugs and the neurotransmitter systems that they target.