Aleksandar Shkondrov

Dr. Aleksandar Shkondrov

Pharmacognosy, Medical University of Sofia, Sofia, Sofia-Grad, Bulgaria
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2016 in Pharmacognosy Reviews
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Journal Article
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IKIlina Nikolaeva Krasteva
Ilina Nikolaeva Krasteva
VBViktor M Bratkov
Viktor M Bratkov
Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
PZPetranka K Zdraveva
Petranka K Zdraveva
Flavonoids, the most common plant polyphenols are widely distributed in every species and possess a broad range of pharmacological activities. The genus Astragalus is the largest in the Fabaceae family with more than 2,500 species spread. They are known to contain different metabolites such as flavonoids, saponins, and polysaccharides. Plants from the genus have been used in the traditional medicine of many countries for centuries. This paper is focused on the large group of flavonoid compounds. Details on structure as well as information about the pharmacological properties of flavonoids, isolated from Astragalus species have been discussed. This review is based on publications until the first half of 2014 and includes also the results from our phytochemical investigations of the genus.

22 March 2014 in Phytochemistry Reviews
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IIIliana Ionkova
Iliana Ionkova
Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
IKIlina Nikolaeva Krasteva
Ilina Nikolaeva Krasteva
TITodor Ionkov
Todor Ionkov

23 November 2018 in Natural Product Research
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Journal Article
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Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
IKIlina Nikolaeva Krasteva
Ilina Nikolaeva Krasteva
Franz BucarFranz Bucar
Franz Bucar
OKOlaf Kunert
Olaf Kunert
MKMagdalena Kondeva-Burdina
Magdalena Kondeva-Burdina
IIIliana Ionkova
Iliana Ionkova
A new tetracyclic saponin, 17(R),20(R)-3β,6α,16β-trihydroxycycloartanyl-23-carboxylic acid 16-lactone 3-O-β-D-glucopyranoside (1) together with one known flavonoid, camelliaside A (2) were isolated from the aerial parts of Astragalus glycyphyllos L. Their structures were determined by chemical, HRESIMS and NMR methods. On 6-hydroxydopamine in vitro model on isolated rat brain synaptosomes, compounds 1–2 had statistically significant neuroprotective activity similar to that of Silibinin, tested at 100 μM. Saponin 1 possessed the most prominent neuroprotective and antioxidant effects in this in vitro model. On human recombinant monoamine oxidase type B enzyme compound 1 displayed strong inhibiting activity, compared to Selegiline (1 μM). It could be concluded that the new epoxycycloartane saponin 1 could be a promising leading structure in respect of neurodegenerative diseases.

1 January 2018 in Food and Chemical Toxicology
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Journal Article
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MKMagdalena Kondeva-Burdina
Magdalena Kondeva-Burdina
Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
Rumyana SimeonovaRumyana Simeonova
Rumyana Simeonova
VVVessela Vitcheva
Vessela Vitcheva
IKIlina Nikolaeva Krasteva
Ilina Nikolaeva Krasteva
IIIliana Ionkova
Iliana Ionkova

19 July 2023 in Metabolites
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ISIvan Stambolov
Ivan Stambolov
Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
OKOlaf Kunert
Olaf Kunert
Franz BucarFranz Bucar
Franz Bucar
MKMagdalena Kondeva-Burdina
Magdalena Kondeva-Burdina
IKIlina Nikolaeva Krasteva
Ilina Nikolaeva Krasteva
Astragalus glycyphyllos (Fabaceae) is used in the traditional medicine of many countries against hepatic and cardiac disorders. The plant contains mainly flavonoids and saponins. From a defatted methanol extract from its overground parts, a new triterpenoid saponin, 3-O-[α-L-rhamnopyranosyl-(1→2)]-β-D-xylopyranosyl]-24-O-α-L-arabinopyranosyl-3β,6α,16β,24(R),25-pentahydroxy-20R-cycloartane, together with the rare saponin astrachrysoside A, were isolated using various chromatography methods. The compounds were identified via extensive high resolution electrospray ionisation mass spectrometry (HRESIMS) and NMR analyses. Both saponins were examined for their possible antioxidant and neuroprotective activity in three different in vitro models. Rat brain synaptosomes, mitochondria, and microsomes were isolated via centrifugation using Percoll gradient. They were treated with the compounds in three different concentrations alone, and in combination with 6-hydroxydopamine or tert-butyl hydroperoxide as toxic agents. It was found that the compounds had statistically significant dose-dependent in vitro protective activity on the sub-cellular fractions. The compounds exhibited a weak inhibitory effect on the enzyme activity of human recombinant monoamine oxidase type B (hMAO-B), compared to selegiline.

26 November 2020 in Pharmacia
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MVMaria Voynova
Maria Voynova
Aleksandar ShkondrovAleksandar Shkondrov
Aleksandar Shkondrov
MKMagdalena Kondeva-Burdina
Magdalena Kondeva-Burdina
IKIlina Krasteva
Ilina Krasteva
Amanita muscaria, commonly known as fly agaric, is a basidiomycete. Its main psychoactive constituents are ibotenic acid and muscimol, both involved in ‘pantherina-muscaria’ poisoning syndrome. The rising pharmacological and toxicological interest based on lots of contradictive opinions concerning the use of Amanita muscaria extracts’ neuroprotective role against some neurodegenerative diseases such as Parkinson’s and Alzheimer’s, its potent role in the treatment of cerebral ischaemia and other socially significant health conditions gave the basis for this review. Facts about Amanita muscaria’s morphology, chemical content, toxicological and pharmacological characteristics and usage from ancient times to present-day’s opportunities in modern medicine are presented.