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QuickView for Dapiprazole (compound)


PubChem
Name: dapiprazole
PubChem Compound ID: 3033538
Molecular formula: C19H27N5
Molecular weight: 325.451 g/mol
Synonyms:
Dapirazolum [INN-Latin]; Reversil; DAPIRAZOLE; Dapirazol [INN-Spanish]; Dapiprazol [German]; 1,2,4-Triazolo(4,3-a)pyridine, 5,6,7,8-tetrahydro-3-(2-(4-(2-methylphenyl)-1-piperazinyl)ethyl)-; 5,6,7,8-Tetrahydro-3-(2-(4-(o-tolyl)-1-piperazinyl)ethyl)-s-triazolo(4,3-a)pyridine; Glamidolo; 72822-12-9; DAPIPRAZOLE
DrugBank
Identification
Name: dapiprazole
Name (isomeric): DB00298
Drug Type: small molecule
Brand: Rev-Eyes
Category: Ophthalmologicals, Antimydriatics, Adrenergic alpha-Antagonists, Antipsychotic Agents
CAS number: 72822-12-9
Pharmacology
Indication: Used in the treatment of iatrogenically induced mydriasis produced by adrenergic (phenylephrine) or parasympatholytic (tropicamide) agents used in certain eye examinations.
Pharmacology:
Dapiprazole is an alpha-adrenergic blocking agent. It produces miosis by blocking the alpha-adrenergic receptors on the dilator muscle of the iris. Dapiprazole produces no significant action on ciliary muscle contraction and thus, there are no changes in the depth of the anterior chamber of the thickness of the lens. It does not alter the IOP eithe...
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Mechanism of Action: Dapiprazole acts through blocking the alpha1-adrenergic receptors in smooth muscle. It produces miosis through an effect on the dilator muscle of the iris and does not have any significant activity on ciliary muscle contraction and, therefore does not induce a significant change in the anterior chamber depth or the thickness of the lens.
Absorption: Systemic absorption is negligible.
Toxicity: Oral LD50 is 1189-2100 mg/kg in mice, rats and rabbits.
Affected organisms: Humans and other mammals
Interactions
Drug interaction:
TamsulosinConcomitant use of alpha1-adrenergic antagonists, Tamsulosin and Dapiprazole, may result in additive antihypertensive effects. Combination therapy is not recommended.

Targets