Английская Википедия:Asarone

Материал из Онлайн справочника
Версия от 07:25, 3 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 457630359 | ImageFileL1 = Alpha-Asaron.svg | ImageSizeL1 = 120px | ImageCaptionL1 = α-Asarone | ImageFileR1 = Beta-Asaron.svg | ImageSizeR1 = 120px | ImageCaptionR1 = β-Asarone | IUPACName = 1,2,4-Trimethoxy-5-[(''E'')-prop-1-enyl]benzene (α)<br>1,2,4-Trimethoxy-5-[(''Z'')-prop-1-enyl]benzene (β) | Oth...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox

Asarone is chemical compound of the phenylpropanoid class found in certain plants such as Acorus and Asarum.[1] There are two isomers, α (or trans) and β (or cis).[2] As a volatile fragrance oil, it is used in killing pests and bacteria.[3]

Pharmacology

The main clinical symptom of asarone is prolonged vomiting that sometimes lasted more than 15 hours. Asarone is not metabolized to trimethoxyamphetamine as has been claimed by online vendors.[4]

The Council of Europe Committee of Experts on Flavouring Substances concluded that β-asarone is clearly carcinogenic[5] and has proposed limits for its concentration in flavorings such as bitters made from Acorus calamus (sweet flag).[6]

β-Asarone exhibits anti-fungal activity by inhibiting ergosterol biosynthesis in Aspergillus niger.[7] However, the toxicity and carcinogenicity of asarone means that it may be difficult to develop any practical medication based on it.[8]

See also

Notes and references

Шаблон:Reflist

  1. Ошибка цитирования Неверный тег <ref>; для сносок merck не указан текст
  2. Beta asarone has CAS# 5273-86-9
  3. Шаблон:Cite journal
  4. Шаблон:Cite journal
  5. Шаблон:Cite journal
  6. Шаблон:Cite journal
  7. Шаблон:Cite journal
  8. Шаблон:Cite journal