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107220-28-0

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107220-28-0 Structure

107220-28-0 Structure
IdentificationBack Directory
[Name]

Cevimeline Hydrochloride Salt
[CAS]

107220-28-0
[Synonyms]

Fks 508
SNK 508
Saligren
Snd 5008
CeviMelin
rac-Cevimeline HCl
AF-102B hydrochloride
SNI-2011 hydrochloride
Cevimelin Hydrochloride
CEVIMELINE, HYDROCHLORIDE SALT
CeviMeline hydrochloride Saligren
rac,cis-Cevimeline Hydrochloride Salt
AF-102B HYDROCHLORIDE;SNI-2011 HYDROCHLORIDE
cis-2-Methylspiro[1,3-oxathiolane-5,3'-quinuclidine]hydrochloride
2-methylspiro[1,3-oxathiolane-5,3'-1-azabicyclo[2.2.2]octane],hydrochloride
(2'R,3R)-rel-2'-Methyl- spiro[1-azabicyclo[2.2.2]octane-3,5'-[1,3]oxathiolane] hydrochloride
[Molecular Formula]

C10H18ClNOS
[MDL Number]

MFCD01961045
[MOL File]

107220-28-0.mol
[Molecular Weight]

235.774
Chemical PropertiesBack Directory
[Melting point ]

195-197?C
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[solubility ]

Water:50.0(Max Conc. mg/mL);212.07(Max Conc. mM)
[form ]

A crystalline solid
[color ]

White to off-white
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[Toxicity]

mouse,LD50,intravenous,33mg/kg (33mg/kg),United States Patent Document. Vol. #4855290,
Hazard InformationBack Directory
[Chemical Properties]

Off-White Solid
[Uses]

A novel muscarinic M1 and M3 receptor agonist. Sialagogue.
[Biological Activity]

Selective M 1 receptor agonist. Induces atropine-sensitive contractions of isolated guinea pig ilea and trachea preparations (EC 50 values are 3.5 and 3 μ M respectively). Reverses AF64A-induced cognitive impairments in vivo .
[in vivo]

Cevimeline (0.008-0.016 mg/kg; intraperitoneal injection; male Wistar rats) treatment shows slowly increasing and lasting salivation, and increased blood flow increment in the parotid gland and pressor response. Cevimeline inhibits angiotensin II-induced water intake and neuronal activity in the subfornical organ at 0.016 mg/kg[1].

Animal Model:Male Wistar rats (8-week-old) injected with angiotensin-II[1]
Dosage:0.008 mg/kg, 0.016 mg/kg
Administration:Intraperitoneal injection
Result:Showed slowly increasing and lasting salivation, and increased blood flow increment in the parotid gland and pressor response.
[IC 50]

mAChR1; mAChR3
[storage]

-20°C
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