Coumarins ofSeseli peucedanoides

Abyshev, A. Z.; Abyshev, D. Z.

doi:10.1007/bf00579495

Cited by 5 publications

(7 citation statements)

References 1 publication

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“…arenarium, S. hartvigii, S. andronakii, S. serpentinum, S. grandivittatum, S. serpentinum, S. globiferum, S. alexeenkoi and S. leptocladum. The existence of two independent species in western Mediterranean and southwest Asia was also confirmed by analysis of coumarine composition since Muckensturm in Reduron (2008) noted that plants from Azerbaijan studied by Abyshev and Abyshev (1984) differ from Portuguese plants of S. tortuosum in this respect. These two species are also very similar in morphological features.…”

Section: The Non-monophyletic Nature Of Seseli Tortuosum Sensu Latomentioning

confidence: 77%

Molecular data to elucidate the taxonomy of Seseli sect. Seseli (Apiaceae) in east Mediterranean and southern Europe

Lyskov

Güner

Samigullin

et al. 2018

Nordic Journal of Botany

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The taxonomy of the type section of the genus Seseli is revised based on newly obtained molecular data. The type species of the genus, Seseli tortuosum, is shown to be a polyphyletic taxon and is split into two species: the western Mediterranean S. tortuosum and the eastern Mediterranean S. arenarium. The Turkish endemics S. hartvigii, S. serpentinum and S. andronakii, and the Transcaucasian S. grandivittatum form a complex of closely related species together with S. arenarium. The results of the molecular analysis confirm the specific rank of S. corymbosum, S. phrygium and S. paphlagonicum and the status of S. gummiferum as distinct from either of these three. The latter species is strictly endemic to Crimea and does not occur in Turkey.

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Section: The Non-monophyletic Nature Of Seseli Tortuosum Sensu Latomentioning

confidence: 77%

Molecular data to elucidate the taxonomy of Seseli sect. Seseli (Apiaceae) in east Mediterranean and southern Europe

Lyskov

Güner

Samigullin

et al. 2018

Nordic Journal of Botany

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“…The same spectrum showed two pair of singlets at δ H 6.69 (1H, s, 1a ) and δ H 7.19 (1H, s, 1a ) and at δ H 6.76 (1H, s, 1b ) and δ H 7.14 (1H, s, 1b ) corresponding to the aromatic protons H-8 and H-5, respectively. The observation in the same spectrum of a triplet at δ H 5.02 (1H, t, J = 9 Hz, H-2', 1a ) and a multiplet at δ H 5.12 (1H, m, H-2', 1a ) a multiplet at δ H 3.10–3.30 (4H, m, H-3'a,b, 1a and 1b ) suggested the presence of the dihydrofuranic moiety in 1a and 1b [17,19,20,21,22,23,24]. These data and the observed duplication of all the signals are in good concordance with the dihydrofuranocoumarin structure of 1a and 1b .…”

Section: Resultsmentioning

confidence: 99%

Chemical Composition, Biological and Cytotoxic Activities of Plant Extracts and Compounds Isolated from Ferula lutea

et al. 2014

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Abstract:The present work describes the phytochemical study on Ferula lutea flowers. Total phenolics and flavonoids of the n-butanol and ethyl acetate extracts were quantified (phenolics [40.68-52.29 mg gallic acid equivalent/g of dry weight], flavonoids [12.38-14.72 mg quercitin/g dry weight]). Two diastereoisomers were isolated and identified using spectroscopic techniques (1D, 2D NMR and GC-MS). The extracts and diastereoisomers were tested for antioxidant, antiacetylcholinesterase, antimicrobial, antidiabectic, cytotoxic (leukemia cell line) activities and allelopathic potentialities. The strongest antioxidant activity was obtained for the ethyl acetate extract (IC 50 = 12.8 ± 1.29 µg/mL). The two extracts exhibited high antidiabetic activity (54.1 and 52.1% at 40 µg/mL).

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“…Chloticol ( 101) is possibly an artefact. '16 The diol monomethyl ether (102) from the same plant not only may be an artefact, since methanol was used for its isolation, but its structure may have to be reassigned as (103) since it gave a monoacetate with acetic anhydride in the ~0 l d . l ~~ In 1984, minumicrolin, m.p.…”

Section: C-substituted 7-oxygenated Coumarinsmentioning

confidence: 99%