incana




(1)
Canberra, Aust Capital Terr, Australia

 




Scientific Name


Matthiola incana (L.) R.Br.


Synonyms


Cheiranthus albus Mill., Cheiranthus annuus L., Cheiranthus coccineus Mill., Cheiranthus incanus L., Cheiranthus fenestralis L., Cheiranthus graecus Pers., Cheiranthus hortensis Lam., Cheiranthus viridis Ehrh., Hesperis fenestralis (L.) Lam., Hesperis incana (L.) Kuntze, Matthiola annua (L.) Sweet, Matthiola fenestralis (L.) R.Br., Mathiolaria annua (L.) Chevall.


Family


Brassicaceae


Common/English Names


Brampton Stock, Common Stock, Gillyflower, Hoary Stock, Imperial Stock, Stock, 10-Week Stock


Vernacular Names






  • Czech: Fiala Šedivá


  • Eastonian: Aedlevkoi


  • Esperanto: Matiolo Nuda


  • Finnish: Tarhaleukoija


  • French: Giroflée, Mattiole Blanchâtre, Voilier Grisâtre


  • German: Garten-Levkoje, Weisslichgraue Levkoje


  • Hungarian: Kerti Viola, Nyári Viola, Szagos Viola


  • Peru: Alhelí (Spanish)


  • Polish: Lewkonia Letnia


  • Portuguese: Goiveiro-Encarnado, Goivo-Encarnado


  • Slovašcina: Fajgelj, Šeboj, Sorta’


  • Slovencina: Fiala Sivá


  • Swedish: Gillyflower, Lövkoja


  • Turkey: Yalancı Şebboy


  • Welsh: Murwyll Coesbren, Murwyll Lledlwyd


Origin/Distribution


It is native to the coastal areas of southern and western Europe and has naturalized elsewhere. It has been introduced into the New World and Australia.


Agroecology


Matthiola incana is a cool climate species, growing best in temperatures of 15–24 °C. It thrives in full sun to light shade and grows best in well-drained, moist, fertile, organic rich soil with a neutral or slightly alkaline pH range.


Edible Plant Parts and Uses


Its flowers are eaten as a vegetable or used as a garnish, especially with sweet desserts (Tanaka 1976; Facciola 1990). Studies reported that M. incana seeds contained oil rich (55–65 %) in omega-3 linolenic acid and could replace marine oils and thereby contribute beneficially to the human diet (Yaniv et al. 1999).


Botany


A biennial or perennial tomentose herb, 15–75 cm high, unbranched or with sparingly basal branching. Basal leaves rosulate; cauline leaves shortly petiolate or sessile, oblanceolate, 3–16 cm long, (0.5-) 1–2 cm broad margin entire; base attenuate to cuneate, apex rounded (Plates 1 and 2). Racemes 10–30-flowered. Flower: sepals linear-lanceolate to narrowly oblong, 10–15 by 2–3 mm; petals purple, violet, pink, red or white (Plates 1, 2 and 3), obovate to ovate, 20–30 by 7–15 mm, long clawed, apex rounded or emarginate; stamens 7–9, filaments 5–8 mm, anthers 2–4 mm; style 1–5 mm, stigma bilobed, erect, sessile. Siliquae (7-) 10–15 cm long, 2.5–4 mm wide, pubescent-glandular. Seed sub-orbicular, 2 mm across, brown, winged.

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Plate 1
Purple flower stock and leaves


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Plate 2
Maroon flower stock and leaves


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Plate 3
Bunch of stock flowers


Nutritive/Medicinal Properties



Phytochemicals in Flowers


The flavonoid glycoside dactylin with the structure 5,7,3,4′- tetrahydroxy-3′-methoxyflavone-3-O-B-d-glucopyranoside was isolated from M. incana (Rahman and Khan 1962). The following phenolic compounds p-coumaric, caffeic, ferulic and sinapic acids and kaempferol and anthocyanin pigments were found in the flowers of healthy and virus-infected plants of Matthiola incana (Feenstra et al. 1963). In healthy red flowers larger amounts of cinnamic acids were present, bound to the acylated anthocyanins and other compounds and possibly also as free acids. When anthocyanin synthesis was blocked, the formation of cinnamic acids was also inhibited, except for small amounts of sinapic and ferulic acids. In anthocyanin-producing flowers of Matthiola incana, the presence of naringenin, naringenin 7-glucoside, dihydrokaempferol and dihydrokaempferol 7-glucoside was detected (Forkmann 1979). The four isolated compounds initiated anthocyanin synthesis after administration to acyanic flowers of genetically defined lines of Matthiola incana and Antirrhinum majus.

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May 21, 2017 | Posted by in PHARMACY | Comments Off on incana

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