trans-Cevimeline Hydrochloride
trans-Cevimeline Hydrochloride Basic information
- Product Name:
- trans-Cevimeline Hydrochloride
- Synonyms:
-
- (2S)-2-methylspiro[1,3-oxathiolane-5,3'-1-azabicyclo[2.2.2]octane]:hydrochloride
- Cevimeline Impurity 7(trans-Cevimeline HCl)
- trans-Cevimeline HCl
- rac,trans-Cevimeline Hydrochloride
- AF 102A HCl
- CAS:
- 107220-29-1
- MF:
- C10H18ClNOS
- MW:
- 235.77402
- Mol File:
- 107220-29-1.mol
trans-Cevimeline Hydrochloride Chemical Properties
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- color
- White to Off-White
- Stability:
- Hygroscopic
trans-Cevimeline Hydrochloride Usage And Synthesis
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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