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107220-29-1

107220-29-1 Structure

107220-29-1 Structure
IdentificationBack Directory
[Name]

trans-Cevimeline Hydrochloride
[CAS]

107220-29-1
[Synonyms]

AF 102A HCl
trans-Cevimeline HCl
rac,trans-Cevimeline Hydrochloride
Cevimeline Impurity 7(trans-Cevimeline HCl)
(2S)-2-methylspiro[1,3-oxathiolane-5,3'-1-azabicyclo[2.2.2]octane]:hydrochloride
[Molecular Formula]

C10H18ClNOS
[MDL Number]

MFCD01961046
[MOL File]

107220-29-1.mol
[Molecular Weight]

235.774
Chemical PropertiesBack Directory
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]


GHS08,GHS06
[Signal word ]

Danger
[Hazard statements ]

H361-H301-H351-H332
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501-P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501-P261-P271-P304+P340-P312
Hazard InformationBack Directory
[Description]

trans-Cevimeline HCl, also known as AF 102A, is the trans-isomer of AF102B (Cevimeline). Cevimeline is a cholinergic analogue with glandular secretion stimulatory activity. Cevimeline binds to and activates muscarinic receptors, thereby increasing the secretions in exocrine salivary and sweat glands. This cholinergic agonist also increases the tone of smooth muscle in the gastrointestinal and urinary tracts. Cevimeline is being studied as a treatment for dry mouth caused by radiation therapy to the head and neck.
[Uses]

trans-Cevimeline Hydrochloride is a reagent in the preparation of spiro-oxathiolane/quinuclidine sulfoxide derivative for the treatment of central nervous and cholinergic system disease or disorders.
[in vivo]

AF102A (1 mg/kg; i.p.) reverses cognitive impairments in a step-through passive avoidance task[1].

Animal Model:Rats[1]
Dosage:1 mg/kg
Administration:I.p.
Result:Reversed cognitive impairments in a step-through passive avoidance task.
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