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Alexandra S Silchenko

Showing results (11-20 of 67) with videos related to

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Natural Product Communications|September 20, 2011
Structure of cucumariosides H5, H6, H7 and H8, triterpene glycosides from the sea cucumber Eupentacta fraudatrix and unprecedented aglycone with 16,22-epoxy-groupAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|October 2, 2013
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological action of cucumariosides I1, I3, I4, three new minor disulfated pentaosidesAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|October 19, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological activity of cucumariosides B1 and B2, two new minor non-sulfated unprecedented triosidesAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|May 12, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological action of cucumariosides A1, A3, A4, A5, A6, A12 and A15, seven new minor non-sulfated tetraosides and unprecedented 25-keto, 27-norholostane aglyconeAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|August 23, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and cytotoxic action of cucumariosides A2, A7, A9, A10, an, A13 and A14, seven new minor non-sulfated tetraosides and an aglycone with an uncommon 18-hydroxy groupAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Research|October 13, 2011
Structures and cytotoxic properties of cucumariosides H₂, H₃ and H₄ from the sea cucumber Eupentacta fraudatrixAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Journal of Natural Products|December 28, 2002
Triterpene glycosides from the deep-water North-Pacific sea cucumber Synallactes nozawai MitsukuriAlexandra S Silchenko, Sergey A Avilov, Alexandr A Antonov, et al.
Marine Drugs|April 3, 2021
Triterpene Glycosides from the Far Eastern Sea Cucumber <i>Thyonidium (=Duasmodactyla) kurilensis</i> (Levin): The Structures, Cytotoxicities, and Biogenesis of Kurilosides A<sub>3</sub>, D<sub>1</sub>, G, H, I, I<sub>1</sub>, J, K, and K<sub>1</sub>Alexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Marine Drugs|April 13, 2018
Holotoxin A₁ Induces Apoptosis by Activating Acid Sphingomyelinase and Neutral Sphingomyelinase in K562 and Human Primary Leukemia CellsSeong-Hoon Yun, Eun-Hye Sim, Sang-Heum Han, et al.
International Journal of Molecular Sciences|November 13, 2025
Anticancer Activity of Triterpene Glycosides Cucumarioside A<sub>0</sub>-1 and Djakonovioside A Against MDA-MB-231 as A<sub>2B</sub> Adenosine Receptor AntagonistsElena A Zelepuga, Ekaterina A Chingizova, Ekaterina S Menchinskaya, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

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Pageof 7
Natural Product Communications|September 20, 2011
Structure of cucumariosides H5, H6, H7 and H8, triterpene glycosides from the sea cucumber Eupentacta fraudatrix and unprecedented aglycone with 16,22-epoxy-groupAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|October 2, 2013
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological action of cucumariosides I1, I3, I4, three new minor disulfated pentaosidesAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|October 19, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological activity of cucumariosides B1 and B2, two new minor non-sulfated unprecedented triosidesAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|May 12, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and biological action of cucumariosides A1, A3, A4, A5, A6, A12 and A15, seven new minor non-sulfated tetraosides and unprecedented 25-keto, 27-norholostane aglyconeAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Communications|August 23, 2012
Triterpene glycosides from the sea cucumber Eupentacta fraudatrix. Structure and cytotoxic action of cucumariosides A2, A7, A9, A10, an, A13 and A14, seven new minor non-sulfated tetraosides and an aglycone with an uncommon 18-hydroxy groupAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Natural Product Research|October 13, 2011
Structures and cytotoxic properties of cucumariosides H₂, H₃ and H₄ from the sea cucumber Eupentacta fraudatrixAlexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Journal of Natural Products|December 28, 2002
Triterpene glycosides from the deep-water North-Pacific sea cucumber Synallactes nozawai MitsukuriAlexandra S Silchenko, Sergey A Avilov, Alexandr A Antonov, et al.
Marine Drugs|April 3, 2021
Triterpene Glycosides from the Far Eastern Sea Cucumber <i>Thyonidium (=Duasmodactyla) kurilensis</i> (Levin): The Structures, Cytotoxicities, and Biogenesis of Kurilosides A<sub>3</sub>, D<sub>1</sub>, G, H, I, I<sub>1</sub>, J, K, and K<sub>1</sub>Alexandra S Silchenko, Anatoly I Kalinovsky, Sergey A Avilov, et al.
Marine Drugs|April 13, 2018
Holotoxin A₁ Induces Apoptosis by Activating Acid Sphingomyelinase and Neutral Sphingomyelinase in K562 and Human Primary Leukemia CellsSeong-Hoon Yun, Eun-Hye Sim, Sang-Heum Han, et al.
International Journal of Molecular Sciences|November 13, 2025
Anticancer Activity of Triterpene Glycosides Cucumarioside A<sub>0</sub>-1 and Djakonovioside A Against MDA-MB-231 as A<sub>2B</sub> Adenosine Receptor AntagonistsElena A Zelepuga, Ekaterina A Chingizova, Ekaterina S Menchinskaya, et al.
Pageof 7