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Showing content from https://en.wikipedia.org/wiki/Thiazinamium below:

Thiazinamium metilsulfate - Wikipedia

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Chemical compound

Pharmaceutical compound

Thiazinamium metilsulfate

Thiazinamium

ATC code IUPAC name CAS Number PubChem CID ChemSpider UNII CompTox Dashboard (EPA) ECHA InfoCard 100.017.320 Formula C18H23N2S+ Molar mass 299.46 g·mol−1 3D model (JSmol) SMILES InChI  NY (what is this?)  (verify)

Thiazinamium metilsulfate (INN) or thiazinam is an antihistamine. The USAN is thiazinamium chloride (with a different counterion).

Since many of the uses of antihistamines involve conditions such as rashes, which should be treatable by local application, there is some rationale for developing drugs for topical use. The known side effects of antihistamines could in principle be avoided if the drug were functionalized to avoid systemic absorption. The known poor absorption of quat salts make such derivatives attractive for nonabsorbable antihistamines for topical use.

Thiazinamium chloride synthesis from promethazine and chloromethane.[1] Acetylcholine receptor modulators Muscarinic acetylcholine receptor modulators mAChRsTooltip Muscarinic acetylcholine receptors Agonists Antagonists Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Nicotinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators
Nicotinic acetylcholine receptor modulators nAChRsTooltip Nicotinic acetylcholine receptors Agonists
(and PAMsTooltip positive allosteric modulators) Antagonists
(and NAMsTooltip negative allosteric modulators) Precursors
(and prodrugs)
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Acetylcholine metabolism/transport modulators
Histamine receptor modulators H1 Agonists Antagonists H2 Agonists Antagonists H3 Agonists Antagonists H4 Agonists Antagonists
See also
Receptor/signaling modulators
Monoamine metabolism modulators
Monoamine reuptake inhibitors

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