CEVIMELINE, HYDROCHLORIDE SALT
CEVIMELINE, HYDROCHLORIDE SALT Basic information
- Product Name:
- CEVIMELINE, HYDROCHLORIDE SALT
- Synonyms:
-
- CevimelineHClSalt
- (+/-)-cis-2-Methylspiro[1,3-oxathiolane-5,3quinuclidine
- Spiro[1-azabicyclo[2.2.2]octane-3,5'-[1,3]oxathiolane], 2'-methyl-, (2'R,3R)-rel-
- Spiro[1-azabicyclo[2.2.2]octane-3,5'-[1,3]oxathiolane], 2'-methyl-, cis-
- 2-methyspiro(1,3-oxathiolane-5,3)quinuclidine
- AF-102B
- Evoxac
- SNI-2011
- CAS:
- 107233-08-9
- MF:
- C10H17NOS
- MW:
- 199.31
- Product Categories:
-
- Heterocycles
- Intermediates & Fine Chemicals
- Neurochemicals
- Pharmaceuticals
- Mol File:
- 107233-08-9.mol
CEVIMELINE, HYDROCHLORIDE SALT Chemical Properties
- Melting point:
- 195-197°C
- Boiling point:
- 308.5±42.0 °C(Predicted)
- Density
- 1.19
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- Soluble in DMSO
- form
- Powder
- pka
- 9.51±0.40(Predicted)
- CAS DataBase Reference
- 107233-08-9
Safety Information
- Hazardous Substances Data
- 107233-08-9(Hazardous Substances Data)
CEVIMELINE, HYDROCHLORIDE SALT Usage And Synthesis
Chemical Properties
Off-White Solid
Uses
A muscarinic M1 and M3 receptor agonist. Sialagogue
Biological Activity
cevimeline is a muscarinic receptor agonist especially on the m1 and m3 receptors. [1]cevimeline has been approved for use against symptoms of dry mouth by activating the m3 receptors of the parasympathetic nervous system. cevimeline is effective and safe in improving symptoms of dry eye with 20 mg three times per day [2]. cevimeline increased the intracellular ca+ level in parotid gland acinar cells over 1 μm and rat, enhanced the excitability via muscarinic receptors, thereby, cevimeline alleviates dry mouth symptoms by stimulating secretion by the salivary glands. cevimeline has a longer duration of salivation[3]. cevimeline plays a part in alzheimer’s disease. cevimeline decreased aβ (1–40) level in the cerebrospinal fluid (csf) at 1 mg/kg without changing α-apps in rabbit and significantly decreased csf aβ in ad patients.[4]
References
1. f. b. vivino, i. al-hashimi, z. khan, f. g. leveque, p. l. salisbury, 3rd, t. k. tran-johnson, c. c. muscoplat, m. trivedi, b. goldlust and s. c. gallagher, arch intern med 1999, 159, 174-181. 2. m. ono, e. takamura, k. shinozaki, t. tsumura, t. hamano, y. yagi and k. tsubota, am j ophthalmol 2004, 138, 6-17. 3. k. ono, t. inagaki, t. iida, r. hosokawa and k. inenaga, j med invest 2009, 56 suppl, 375. 4. a. fisher, z. pittel, r. haring, n. bar-ner, m. kliger-spatz, n. natan, i. egozi, h. sonego, i. marcovitch and r. brandeis, j mol neurosci 2003, 20, 349-356.
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