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2018年5月6日星期日

Original: A-804598 1125758-85-1, stock more than 100g

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Description: A-804598 is a P2X7 selective, competitive antagonist.
Name: A-804598 
CAS#: 1125758-85-1 
Chemical Formula: C19H17N5 
Exact Mass: 315.1484 
Molecular Weight: 315.38 
Elemental Analysis: C, 72.36; H, 5.43; N, 22.21

Synonym: A-804598; A 804598; A804598.
IUPAC/Chemical Name: N-Cyano-N′′-[(1S)-1-phenylethyl]-N′-5-quinolinyl-guanidine
InChi Key: PQYCRDPLPKGSME-AWEZNQCLSA-N
InChi Code: InChI=1S/C19H17N5/c1-14(15-7-3-2-4-8-15)23-19(22-13-20)24-18-11-5-10-17-16(18)9-6-12-21-17/h2-12,14H,1H3,(H2,22,23,24)/t14-/m0/s1
SMILES Code: C[C@H](/N=C(NC1=C2C=CC=NC2=CC=C1)/NC#N)C3=CC=CC=C3

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO
Shelf Life: >2 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
Harmonized System Code: 293490

REFERENCES
1: Lord B, Ameriks MK, Wang Q, Fourgeaud L, Vliegen M, Verluyten W, Haspeslagh P, 
Carruthers NI, Lovenberg TW, Bonaventure P, Letavic MA, Bhattacharya A. A novel 
radioligand for the ATP-gated ion channel P2X7: [3H] JNJ-54232334. Eur J 
Pharmacol. 2015 Oct 15;765:551-9. doi: 10.1016/j.ejphar.2015.09.026. PubMed PMID: 
26386289.
2: Antonioli L, Giron MC, Colucci R, Pellegrini C, Sacco D, Caputi V, Orso G, 
Tuccori M, Scarpignato C, Blandizzi C, Fornai M. Involvement of the P2X7 
purinergic receptor in colonic motor dysfunction associated with bowel 
inflammation in rats. PLoS One. 2014 Dec 30;9(12):e116253. doi: 
10.1371/journal.pone.0116253. PubMed PMID: 25549098; PubMed Central PMCID: 
PMC4280204.
3: Catanzaro JM, Hueston CM, Deak MM, Deak T. The impact of the P2X7 receptor 
antagonist A-804598 on neuroimmune and behavioral consequences of stress. Behav 
Pharmacol. 2014 Sep;25(5-6):582-98. doi: 10.1097/FBP.0000000000000072. PubMed 
PMID: 25083574.
4: Able SL, Fish RL, Bye H, Booth L, Logan YR, Nathaniel C, Hayter P, Katugampola 
SD. Receptor localization, native tissue binding and ex vivo occupancy for 
centrally penetrant P2X7 antagonists in the rat. Br J Pharmacol. 2011 
Jan;162(2):405-14. doi: 10.1111/j.1476-5381.2010.01025.x. PubMed PMID: 20840537; 
PubMed Central PMCID: PMC3031061.
5: Donnelly-Roberts DL, Namovic MT, Surber B, Vaidyanathan SX, Perez-Medrano A, 
Wang Y, Carroll WA, Jarvis MF. [3H]A-804598 
([3H]2-cyano-1-[(1S)-1-phenylethyl]-3-quinolin-5-ylguanidine) is a novel, potent, 
and selective antagonist radioligand for P2X7 receptors. Neuropharmacology. 2009 
Jan;56(1):223-9. doi: 10.1016/j.neuropharm.2008.06.012. PubMed PMID: 18602931.