File:Albendazole.svg · Wikimedia Commons · See Wikimedia Commons
albendazol
Sign in to saveAlso known as SK&F 62979, SK&F-62979, O-methyl N-(5-(propylthio)-2-benzimidazolyl)carbamate, 5-(propylthio)-2-carbomethoxyaminobenzimidazole, [5-(propylthio)-1H-benzimidazol-2-yl]carbamic acid methyl ester, O-methyl N-[5-(propylthio)-2-benzimidazolyl]carbamate, albendazole
Albendazole is a broad-spectrum antihelmintic and antiprotozoal agent of the benzimidazole type. It is used for the treatment of a variety of intestinal parasite infections, including ascariasis, pinworm infection, hookworm infection, trichuriasis, strongyloidiasis, taeniasis, clonorchiasis, opisthorchiasis, cutaneous larva migrans, giardiasis, and gnathostomiasis, among other diseases.
OverviewAI-generated
Albendazol is a chemical compound with the formula C₁₂H₁₅N₃O₂S. Its IUPAC name is methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate. The substance has a mass of 265.088498 and a weight of 265.33. It features a melting point of 209 and a defined daily dose of 0.4.
Physicochemical properties include an xlogp of 2.9 and a topological polar surface area of 92.3. The molecule contains two hydrogen bond donors and four hydrogen bond acceptors, with a charge of 0. The canonical SMILES notation for the compound is CCCSC1=CC2=C(C=C1)N=C(N2)NC(=O)OC.
Albendazol is associated with a PubMed query count of 8754. It is referenced by 212 other encyclopedia articles.
Synthesized by Vinony from 19 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Key facts
- Drug.Watchedfields
- changed
- Drug.verifiedrevid
- 477316402
- Drug.image
- Albendazole.svg
- Drug.image_class
- skin-invert-image
- Drug.image2
- Albendazole-from-xtal-2007-3D-balls.png
- Drug.image_class2
- bg-transparent
- Drug.width2
- 250
- Drug.tradename
- Albenza, others
- Drug.MedlinePlus
- a610019
- Drug.DailyMedID
- Albendazole
- Drug.pregnancy_AU
- D
- Drug.routes_of_administration
- By mouth
- Drug.ATC_prefix
- P02
- Drug.ATC_suffix
- CA03
- Drug.legal_AU
- S4
- Drug.legal_CA
- Rx-only
- Drug.legal_UK
- POM
- Drug.legal_US
- Rx-only
via Wikipedia infobox
Chemical data
- Formula
- C12H15N3O2S
- Molecular weight
- 265.33 g/mol
- IUPAC name
- methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate
- SMILES
- CCCSC1=CC2=C(C=C1)N=C(N2)NC(=O)OC
- InChIKey
- HXHWSAZORRCQMX-UHFFFAOYSA-N
- XLogP
- 2.9
- Polar surface area
- 92.3 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Research
8,754 papers- Albendazole.The Journal of antimicrobial chemotherapy · 1998
- Albendazole-Induced Liver Injury.American journal of therapeutics · 2021
- Albendazole.Indian pediatrics · 1993
- Praziquantel vs. albendazol for cysticercosis.Neurosurgery · 1988
- Therapy for neurocysticercosis.Expert review of neurotherapeutics · 2004
via PubMed
~27 min read
Encyclopedic overview
18 sectionsContents
- Medical uses
- Ivermectin/albendazole
- Contraindications
- Side effects
- Pregnancy
- Overdose
- Interactions
- Pharmacology
- Mechanism of action
- Pharmacokinetics
- History
- Society and culture
- Economics
- Brand names
- Research
- Veterinary use
- Meat
- References
Albendazole is a broad-spectrum antihelmintic and antiprotozoal agent of the benzimidazole type. It is used for the treatment of a variety of intestinal parasite infections, including ascariasis, pinworm infection, hookworm infection, trichuriasis, strongyloidiasis, taeniasis, clonorchiasis, opisthorchiasis, cutaneous larva migrans, giardiasis, and gnathostomiasis, among other diseases.
Common side effects include nausea, abdominal pain, and headache. Rare but potentially serious side effects include bone marrow suppression which usually improves on discontinuing the medication. Liver inflammation has been reported and those with prior liver problems are at greater risk. It is pregnancy category D in Australia, meaning it may cause harm if taken by pregnant women.
Excerpted from Wikipedia’s “albendazol” article, available under the CC BY-SA 4.0 licence.