Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C19H20N2O3
- Molecular weight
- 324.4 g/mol
- IUPAC name
- [(7R)-10-oxo-8-azatricyclo[5.3.1.03,8]undecan-5-yl] 1H-indole-3-carboxylate
- SMILES
- C1[C@@H]2CC(CC3N2CC(=O)C1C3)OC(=O)C4=CNC5=CC=CC=C54
- InChIKey
- UKTAZPQNNNJVKR-DBBXXEFVSA-N
- XLogP
- 3.4
- Polar surface area
- 62.4 Ų
- H-bond donors
- 1
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1997
- Admin. routes
- oral, parenteral
- Indications
- fibromyalgia, Chemotherapy-induced nausea and vomiting, Nausea
via ChEMBL · EBI
Research
313 papers- Dolasetron.2006
- Dolasetron. A review of its pharmacology and therapeutic potential in the management of nausea and vomiting induced by chemotherapy, radiotherapy or surgery.Drugs · 1997
- Dolasetron overdose resulting in prolonged QTc interval and severe hypotension: a case report and literature review.Emergency medicine journal : EMJ · 2007
- Dolasetron: a new option for nausea and vomiting.Journal of the American Animal Hospital Association · 2000
- Drugs for preventing postoperative nausea and vomiting in adults after general anaesthesia: a network meta-analysis.The Cochrane database of systematic reviews · 2020
via PubMed
Wikidata facts
- Has part
- hydrogen
- Mass
- 324.1473925
- Has use
- medication
Show 7 more facts
- canonical SMILES
- O=C(OC1CC2CC3CC(C1)N2CC3=O)c1c[nH]c2ccccc12
- chemical formula
- C₁₉H₂₀N₂O₃
- medical condition treated
- vomiting
- World Health Organisation international non-proprietary name
- dolasetron
- isomeric SMILES
- O=C(O[C@@H]1C[C@@H]2C[C@H]3C[C@H](C1)N2CC3=O)c4c[nH]c5ccccc45
- NCI Thesaurus ID
- C61735
- subject has role
- antiemetic
Sources (2)
via Wikidata · CC0
Article · Deutsch
Dolasetron ist ein 5-HT3-Antagonist zur Behandlung von Übelkeit und Erbrechen in der Chemotherapie und bei PONV. Dolasetron wird in einer Dosierung von 50 bis 200 Milligramm verabreicht. Die Halbwertszeit beträgt 7 bis 9 Stunden. Der Abbau erfolgt über das Enzym Cytochrom P450 2D6. Auch in der Tiermedizin wird es gegen Erbrechen angewendet.
Abstract from DBpedia / Wikipedia · CC BY-SA
Available in 18 languages
- Español
- Français
- Deutsch
- 中文
- Русский
- Português
- العربية
- Bahasa Indonesia
- Nederlands
- Odia
- Romanian
- Serbian
- Serbian (Latin)
- Tiếng Việt
- Türkçe
- Welsh
- فارسی
via Wikidata sitelinks · CC0