Английская Википедия:Griseoxanthone C

Материал из Онлайн справочника
Версия от 04:28, 17 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Short description|Chemical compound found in some lichens}} {{Chembox <!-- Images --> | ImageFile = Griseoxanthone.png | ImageSize = <!-- Names --> | IUPACName = 1,6-Dihydroxy-3-methoxy-8-methylxanthen-9-one | OtherNames = <!-- Sections --> | Section1 = {{Chembox Identifiers | CASNo = 3569-83-3 | ChEBI = | ChEMBL = | ChemSpiderID = | DrugBank = | EC_number = | PubChem = | In...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Short description Шаблон:Chembox

Griseoxanthone C is an organic compound in the structural class of chemicals known as xanthones. Its chemical formula is 1,6-dihydroxy-3-methoxy-8-methylxanthen-9-one, and its molecular formula is C15H12O5. It is found in a plant and some fungi, including a lichen.

History

Griseoxanthone C was first isolated from the fungus Penicillium patulum by McMaster and colleagues in 1960. They were investigating the biosynthesis of the somewhat structurally related compound griseofulvin and discovered it in the residual material of the growth medium containing the fungi.[1] A year later, another group studying griseofulvin biosynthesis discovered that the production of griseoxanthone C could be induced by inhibiting the chlorination of griseophenone C (an intermediate in the biosynthetic pathway leading to griseofulvin), and that griseoxanthone C could be created chemically from griseophenone C.[2] Jayalakshmi and colleagues proposed a chemical synthesis of griseoxanthone C in 1974.[3]

Properties

In its purified form, griseoxanthone C exists as yellowish needles with a melting point of Шаблон:Convert. An ethanolic solution of griseoxanthone C reacts with iron(III) chloride to produce a violet-brown colour. Its ultraviolet spectrum has four peaks of maximum absorption (λmax) at 242, 269, 309, and 340 nm.[4]

In laboratory tests, griseoxanthone C showed strong antibiotic effects toward Bacillus subtilis and methicillin-resistant Staphylococcus aureus.[5] It also has strong cytotoxicity to Hep2 liver cancer cells in in vitro experiments.[6]

Occurrence

In 1992, John Elix and Caroline Crook reported griseoxanthone C from the lichen Lecanora vinetorum.[7] It has since been reported from various other species, including the flowers of the plant Ficus hookeriana,[8] the fungi Fusarium equiseti,[9] Penicillium concentricum,[10] and Urocladium.[5]

See also

References

Шаблон:Reflist

  1. Ошибка цитирования Неверный тег <ref>; для сносок McMaster et al. 1960 не указан текст
  2. Ошибка цитирования Неверный тег <ref>; для сносок Rhodes et al. 1961 не указан текст
  3. Ошибка цитирования Неверный тег <ref>; для сносок Jayalakshmi et al. 1974 не указан текст
  4. Ошибка цитирования Неверный тег <ref>; для сносок Huneck 1996 не указан текст
  5. 5,0 5,1 Ошибка цитирования Неверный тег <ref>; для сносок Wang et al. 2012 не указан текст
  6. Ошибка цитирования Неверный тег <ref>; для сносок Hawas et al. 2018 не указан текст
  7. Ошибка цитирования Неверный тег <ref>; для сносок Elix & Crook 1992 не указан текст
  8. Ошибка цитирования Неверный тег <ref>; для сносок Wei et al. 2012 не указан текст
  9. Ошибка цитирования Неверный тег <ref>; для сносок Hawas et al. 2016 не указан текст
  10. Ошибка цитирования Неверный тег <ref>; для сносок Ali et al. 2017 не указан текст