Structure via PubChem · Public domain (PubChem)
Allicin
Sign in to saveAlso known as thio-2-propene-1-sulfinic acid S-allyl ester
organische schwefelhaltige Verbindung, Vorstufe für knoblauchtypische Duftstoffe
Chemical data
- Formula
- C6H10OS2
- Molecular weight
- 162.3 g/mol
- IUPAC name
- 3-prop-2-enylsulfinylsulfanylprop-1-ene
- SMILES
- C=CCSS(=O)CC=C
- InChIKey
- JDLKFOPOAOFWQN-UHFFFAOYSA-N
- XLogP
- 1.3
- Polar surface area
- 61.6 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Research
1,389 papers- Allicin: chemistry and biological properties.Molecules (Basel, Switzerland) · 2014
- Allicin ameliorates imiquimod-induced psoriasis-like skin inflammation via disturbing the interaction of keratinocytes with IL-17A.British journal of pharmacology · 2023
- Allicin and Cancer Hallmarks.Molecules (Basel, Switzerland) · 2024
- Allicin alleviates traumatic brain injury-induced neuroinflammation by enhancing PKC-δ-mediated mitophagy.Phytomedicine : international journal of phytotherapy and phytopharmacology · 2025
- Allicin: a promising modulator of apoptosis and survival signaling in cancer.Medical oncology (Northwood, London, England) · 2024
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 162.017307
Show 5 more facts
- Commons category
- Allicin
- chemical formula
- C₆H₁₀OS₂
- found in taxon
- Allium sativum
- canonical SMILES
- C=CCSS(=O)CC=C
- physically interacts with
- Transient receptor potential cation channel subfamily V member 1
via Wikidata · CC0
Article · Deutsch
Allicin ist das Umsetzungsprodukt der in Knoblauch vorkommenden nicht-proteinogenen Aminosäure Alliin. Da Allicin nicht stabil ist, wandelt es sich zum Teil spontan in Di- und Trisulfide, im Öl auch in sowie um. Erst diese Verbindungen sind für den typischen Knoblauchgeruch verantwortlich.
Abstract from DBpedia / Wikipedia · CC BY-SA