What is QMPSB(312606-87-4)? -APICDMO

1. QMPSB CAS:312606-87-4 APICDMO is the professional manufacturer of QMPSB and accept Synthetic customization. These products are for scientific research purposes only and not for sale to individuals. QMPSB Reviews QMPSB is an arylsulfonamide-based synthetic cannabinoid that has been sold as a designer drug. QMPSB was first discovered by Nathalie Lambeng and colleagues in 2007. It acts as a full agonist of the CB1 receptor and CB2 receptor with Ki values of 3 nM and 4 nM, respectively.Many related derivatives were subsequently produced, with the main focus of this work being to increase selectivity for the non-psychoactive CB2 receptor.This work led on from an earlier series of sulfamoyl benzamide derivatives for which a patent was filed in 2004. The quinolin-8-yl ester motif of QMPSB led to the discovery of other designer cannabinoids such as PB-22 and BB-22. QMPSB (312606-87-4) Information Product CAS Number Formula Molar mass PubChem CID ChemSpider UNII CompTox Dashboard(EPA) QMPSB 312606-87-4 C22H22N2O4S 410.49 g·mol−1 3929482 3151524 55Q8B94HS5 ChEMBL245876 Reference www.apicdmo.com JINAN APICDMO BIOTECHNOLOGY CO., LIMITED Tel: +8613682461609 Email: emily@apicdmo.com

2. [1] Blakey K, Boyd S, Atkinson S, Wolf J, Slottje PM, Goodchild K, McGowan J (March 2016). “Identification of the novel synthetic cannabimimetic 8-quinolinyl 4-methyl-3-(1-piperidinylsulfonyl)benzoate (QMPSB) and other designer drugs in herbal incense”. Forensic Science doi:10.1016/j.forsciint.2015.12.001. PMID 26795397. International. 260: 40–53. [2] Lambeng N, Lebon F, Christophe B, Burton M, De Ryck M, Quéré L (January 2007). “Arylsulfonamides as a new class of cannabinoid CB1 receptor ligands: identification of a lead and initial SAR studies”. Bioorganic & Medicinal Chemistry Letters. 17 (1): 272–7. doi:10.1016/j.bmcl.2006.09.049. PMID 17027269. [3] Ermann M, Riether D, Walker ER, Mushi IF, Jenkins JE, Noya-Marino B, et al. (March 2008). “Arylsulfonamide CB2 receptor agonists: SAR and optimization of CB2 selectivity”. Bioorganic & Medicinal Chemistry Letters. 18 (5): 1725–9. doi:10.1016/j.bmcl.2008.01.042. PMID 18255291. [4] Worm K, Zhou QJ, Saeui CT, Green RC, Cassel JA, Stabley GJ, et al. (May 2008). “Sulfamoyl benzamides as novel CB2 cannabinoid receptor ligands”. Bioorganic & Medicinal Chemistry 2830–5.doi:10.1016/j.bmcl.2008.04.006. PMID 18430570. Letters. 18 (9): [5] Goodman AJ, Ajello CW, Worm K, Le Bourdonnec B, Savolainen MA, O’Hare H, et al. (January 2009). “CB2 selective sulfamoyl benzamides: optimization of the amide functionality”. Bioorganic & Medicinal Chemistry Letters. 19 (2): 309–13. doi:10.1016/j.bmcl.2008.11.091. PMID 19091565. [6] Sellitto I, Le Bourdonnec B, Worm K, GoodmanA, Savolainen MA, Chu GH, et al. (January 2010). “Novel sulfamoyl benzamides as selective CB(2) agonists with improved in vitro metabolic stability”. Bioorganic & Medicinal Chemistry Letters. 20 (1): 387–91. doi:10.1016/j.bmcl.2009.10.062. PMID 19919895. [7] US application 7297796, Roland E. Dolle, Karin Worm, Q. Jean Zhou, “Sulfamoyl benzamide derivatives and methods of their use”, published Nov 20, 2007, assigned to Adolor Corporation [8] Brandt SD, Kavanagh PV, Westphal F, Dreiseitel W, Dowling G, Bowden MJ, Williamson JP (2020). “Synthetic cannabinoid receptor agonists: analytical profiles and development of QMPSB, QMMSB, QMPCB, 2F-QMPSB, QMiPSB, and SGT-233”. Drug Testing and doi:10.1002/dta.2913. PMID 32880103. Analysis. 13 (1): 175–196. www.apicdmo.com JINAN APICDMO BIOTECHNOLOGY CO., LIMITED Tel: +8613682461609 Email: emily@apicdmo.com