Cyclopentolate Hydrochloride
Ophthalmic examination requires a dilated pupil and a temporarily paralysed ciliary muscle, and cyclopentolate hydrochloride provides both. Applied as eye drops, the agent blocks muscarinic acetylcholine receptors in the iris sphincter and ciliary body, producing mydriasis together with cycloplegia, the loss of accommodation that permits accurate refraction. Compared with atropine, onset is faster and duration considerably shorter, which limits the period of blurred near vision after an examination. The salt form is the standard presentation for topical ocular use, and the antimuscarinic mechanism is shared with atropine even though the kinetics differ. Chemically it is C17H26ClNO3 with a molecular weight of about 327.8 g/mol, approved and developed through the final clinical phase.
The hydrochloride salt formulation of cyclopentolate, a mydriatic and cycloplegic agent used as eye drops to dilate the pupil and temporarily paralyze accommodation for eye examinations. It has a faster onset and shorter duration than atropine.
Berat Molekul
327,8000 g/mol
TPSA
49,80 Ų
Area Terapeutik
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Struktur 2D
Cite this structure
Embed this structure
SMILES
CN(C)CCOC(=O)C(c1ccccc1)C1(O)CCCC1.Cl
InChI
InChI=1S/C17H25NO3.ClH/c1-18(2)12-13-21-16(19)15(14-8-4-3-5-9-14)17(20)10-6-7-11-17;/h3-5,8-9,15,20H,6-7,10-13H2,1-2H3;1H
Molecular Formula
C17H26ClNO3
HBD / HBA
2 / 4
Ikatan yang Dapat Dirotasi
7
Atom Berat
22
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Pertanyaan yang Sering Diajukan
The hydrochloride salt formulation of cyclopentolate, a mydriatic and cycloplegic agent used as eye drops to dilate the pupil and temporarily paralyze accommodation for eye examinations. It has a faster onset and shorter duration than atropine.
Yes, Cyclopentolate Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200473. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 22162. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.
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