Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Alvameline
Price:
Purity: 98.0%
Stocking Period: 10 Day
Contact: Yang

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: ALVAMELINE
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Ms Wang

120241-31-8

120241-31-8 structure

120241-31-8 structure

Name: Alvameline
Chemical Name: 5-(2-ethyltetrazol-5-yl)-1-methyl-3,6-dihydro-2H-pyridine
CAS Number: 120241-31-8
Molecular Formula: C₉H₁₅N₅
Molecular Weight: 193.24900
Catalog: Signaling Pathways GPCR/G Protein mAChR
Create Date: 2018-12-15 17:55:40
Modify Date: 2024-01-09 18:19:03
Alvameline (Lu25-109) is a partial M1 agonist and M2/M3 antagonist.

Name	5-(2-ethyltetrazol-5-yl)-1-methyl-3,6-dihydro-2H-pyridine
Synonyms	Alvameline Alvameline [INN] UNII-4XFD7B36M6

Description	Alvameline (Lu25-109) is a partial M1 agonist and M2/M3 antagonist.
Related Catalog	Signaling Pathways >> GPCR/G Protein >> mAChR Signaling Pathways >> Neuronal Signaling >> mAChR Research Areas >> Neurological Disease
In Vitro	Alvameline is metabolized by human liver microsomes to Lu 31-126 mainly by CYP2D6; to Lu 29-297 and Lu 25-077 mainly by CYP1A2, CYP2A6, CYP2C19, and CYP3A4; and to Lu 32-181 by CYP1A2 and possibly by CYP2C19. One metabolite, Lu 32-181, could be reduced back to alvameline, a reaction not inhibited by the applied cytochrome P-450 inhibitors[1].
In Vivo	Alvameline competitively and effectively antagonizes carbachol-induced contractions and contractions induced by electrical field stimulation in human detrusor muscle. Alvameline produces a concentration-dependent rightward shift of the concentration-response curves for carbachol in both human and pig detrusor, the pKb values being 6.2 and 5.8. Contractions induced by electrical field stimulation in human detrusor are almost completely inhibited by 100 μM alvameline. In contrast, electrical field stimulation-induced contractions in pig detrusor are less sensitive to alvameline, resulting in a final inhibition of 32% with the highest concentration used (100 μM)[2]. Alvameline has been shown to improve cognitivefunction following traumatic brain injury in rats. Alvameline treated rats causes a 13% and 5% decrease in the medial septal nucleus, a 48 and 23% decrease in the vertical limb nucleus of the diagonal band, and a 51 and 28% decrease in the nucleus basalis magnocellularis, respectively[3].
Animal Admin	Rats: Treatment with alvameline is initiated 24 h following TBI and rats are injected (sc) once daily for the first 15 days after injury or sham injury. Injured rats are injected daily with either saline or 15 μmol/kg of alvameline. Sham-injured rats are injected (sc) daily with either saline or 15 μmol/kg of alvameline-T[2].
References	[1]. Jensen KG, et al. In vitro metabolism of the M1-muscarinic agonist 5-(2-ethyl-2H-tetrazol-5-yl)-1-methyl-1,2,3,6-tetrahydropyridine by human hepatic cytochromes P-450 determined at pH 7.4 and 8.5. Drug Metab Dispos. 1999 Jan;27(1):125-32. [2]. Waldeck K, et al. Actions of the new antimuscarinic compound Alvameline on isolated human and pig detrusor. Neurourol Urodyn. 2002;21(1):92-8. [3]. Pike BR, et al. Chronic administration of a partial muscarinic M1 receptor agonist attenuates decreases in forebrain choline acetyltransferase immunoreactivity following experimental brain trauma. Exp Neurol. 1997 Sep;147(1):55-65.

Density	1.25g/cm3
Boiling Point	342.1ºC at 760mmHg
Molecular Formula	C₉H₁₅N₅
Molecular Weight	193.24900
Flash Point	160.7ºC
Exact Mass	193.13300
PSA	46.84000
LogP	0.34980
Vapour Pressure	7.7E-05mmHg at 25°C
Index of Refraction	1.639