Skip to content

Sections

Maps Timeline Graph Cosmos Life Culture Innovation People Climate Trends Art

Browse Dictionary Books Food Places Asteroids Exoplanets Artists Albums Gazetteer Search

© 2026 Vinony · Knowledge from Wikipedia, Wikidata, and 27 public APIs.

後馬托品 · Vinony

Home
Drugboxes which contain changes to verified fields
後馬托品

🌐中文

English Bahasa Indonesia Deutsch Español Français Italiano Nederlands Polski Português Svenska Tiếng Việt Türkçe Русский العربية فارسی 中文日本語

後馬托品

EntityQ1038115· pop 20· linked from 427 articles

後馬托品

Also known as 2-hydroxy-2-phenylacetic acid [(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] ester, (1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-hydroxy-2-phenylacetate

Homatropine (Equipin, Isopto Homatropine) is an anticholinergic medication that is an antagonist at muscarinic acetylcholine receptors and thus the parasympathetic nervous system. It is used in eye drops as a cycloplegic (to temporarily paralyze accommodation), and as a mydriatic (to dilate the pupil).

Key facts

Drug.Verifiedfields: changed
Drug.Watchedfields: changed
Drug.verifiedrevid: 461770217
Drug.image: Homatropine.svg
Drug.image_class: skin-invert-image
Drug.MedlinePlus: a601006
Drug.legal_status: Rx only
Drug.CAS_number: 87-00-3
Drug.ATC_prefix: S01
Drug.ATC_suffix: FA05
Drug.PubChem: 6321423
Drug.DrugBank: DB00725
Drug.ChemSpiderID

Available in 19 languages

Español
Français
Русский
Português
Italiano
العربية
azb
Bahasa Indonesia
Finnish
Hungarian
Nederlands

Connections

Categories

Drugboxes which contain changes to verified fields Drugboxes which contain changes to watched fields Drugs developed by Pfizer Drugs with non-standard legal status ECHA InfoCard ID from Wikidata M1 receptor antagonists M2 receptor antagonists M3 receptor antagonists M4 receptor antagonists M5 receptor antagonists Ophthalmology drugs Tropanes

Sources

wikipedia.externallinksexternallink

16498795

Drug.UNII

8QS6WCL55Z

Drug.ChEMBL

1233442

Drug.IUPAC_name

(N-Methyl-8-azabicyclo[3.2.1]oct-3-yl) 2-hydroxy-2-phenylacetate

Drug.C

16

Drug.H

21

via Wikipedia infobox

Chemical data

Formula: C16H21NO3
Molecular weight: 275.34 g/mol
IUPAC name: [(1S,5R)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2-hydroxy-2-phenylacetate
SMILES: CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(C3=CC=CC=C3)O
InChIKey: ZTVIKZXZYLEVOL-DGKWVBSXSA-N
XLogP: 1.9
Polar surface area: 49.8 Å²
H-bond donors: 1
H-bond acceptors: 4
Formal charge: 0

via PubChem

Research

321 papers

Homatropine.2006
Systemic toxicity from ocular homatropine.Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 1996
Treatment of Non-Infectious Corneal Injury: Review of Diagnostic Agents, Therapeutic Medications, and Future Targets.Drugs · 2022
The interaction between homatropine and optical blur on choroidal thickness.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2018
Comparing homatropine and atropine in pediatric cycloplegic refractions.Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus · 2011

Wikidata facts

Mass: 275.152144

Show 4 more facts

canonical SMILES: CN1C2CCC1CC(C2)OC(=O)C(C3=CC=CC=C3)O
chemical formula: C₁₆H₂₁NO₃
isomeric SMILES: CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(C3=CC=CC=C3)O
Commons category: Homatropine

Sources (1)

wikidata.org

via Wikidata · CC0

Serbian (Latin)

via Wikidata sitelinks · CC0

L-scopolamine

Entity

muscarinic acetylcholine receptor family

homatropine methylbromide

World Health Organization

digital object identifier

chemical formula

central nervous system

myasthenia gravis

Sign in to save

Similar entities

Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).

Entitydist 0.43

Entitydist 0.46

Entitydist 0.47

Entitydist 0.50

Entitydist 0.50

Entitydist 0.50

Entitydist 0.52

Entitydist 0.54

Entitydist 0.54

Entitydist 0.55

Entitydist 0.55

Entitydist 0.55

What links here427 pages

cyclobenzaprine

oxyphenonium bromide

phosphatidylcholine

sn-glycero-3-phosphocholine