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Medicinal Chemistry

Molecular Weight 289.37
Molecular Formula C17H23NO3
IUPAC Name
(8-methyl-8-azabicyclo[3.2.1]oct-3-yl) 3-hydroxy-2-phenylpropanoate

Pharmacognosy

Biological Source

Atropa belladonna, Datura stramonium

Active Constituents

dl-hyoscyamine

Pharmacology & Synthesis

Mechanism of Action

Competitive antagonist at muscarinic acetylcholine receptors.

Pharmacokinetics (ADME)

A: Rapid and complete from GI tract.
D: Widely distributed, crosses BBB.
M: Hepatic hydrolysis and glucuronidation.
E: Renal (30-50% unchanged).

Pharmacodynamics

Increases heart rate, relaxes smooth muscles, decreases exocrine secretions, causes mydriasis.

Synthesis Pathway

Biosynthesized from L-ornithine and phenylalanine via tropine.

Safety, Warnings & Interactions

Adverse Effects

Dry mouth, blurred vision, tachycardia, urinary retention.

Contraindications

Narrow-angle glaucoma, prostatic hypertrophy.

Drug Interactions

Additive anticholinergic effects with TCAs, phenothiazines.

Pharmaceutics & Compendia

Dosage Forms Injection, Ophthalmic drops, Tablets
Official Compendia IP, BP, USP
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