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Hasmik V. Jughetsyan
Observed name:
Jughetsyan, Hasmik V.
Institutions:
A. Mnjoyan Institute of Fine Organic Chemistry,
Scientific Technological Center of Organic and Pharmaceutical Chemistry,
National Academy of Sciences of Armenia
Observed institutions:
A. Mnjoyan Institute of Fine Organic Chemistry,
Scientific Technological Center of Organic and Pharmaceutical Chemistry,
National Academy of Sciences of Armenia
ORCID:
0009-0006-1127-9950
Observed ORCID:
0009-0006-1127-9950
OpenAlex ID:
A5114314547
New triazole-based hybrids as neurotropic agents
2024
·
Samvel N. Sirakanyan
, Domenico Spinelli
, et al.
·
RSC Advances
·
7
PDF
Synthesis and Rearrangement of New 1,3-Diamino-2,7-naphthyridines and 1-Amino-3-oxo-2,7-naphthyridines
2024
·
Samvel N. Sirakanyan
, Domenico Spinelli
, et al.
·
International Journal of Molecular Sciences
·
5
PDF
Synthesis and Neurotropic Activity of New 5-Piperazinopyrazolo[3,4-c]-2,7-naphthyridines and Isoxazolo[5,4-c]-2,7-naphthyridines
2025
·
Samvel N. Sirakanyan
, Elmira K. Hakobyan
, et al.
·
Pharmaceuticals
·
4
PDF
Synthesis and structure of 7-alkyl-5-amino-6,7,8,9-tetrahydroisoxazolo[5,4-c]-2,7-naphthyridines
2026
·
Samvel N. Sirakanyan
, Elmira K. Hakobyan
, et al.
·
Results in Chemistry
·
1
A Universal Method for the Synthesis of new Heterocyclic Systems: Pyrimido[2,1‐ f ][1,2,4]triazines
2025
·
Samvel N. Sirakanyan
, Domenico Spinelli
, et al.
·
ChemistryOpen
·
1
PDF
Design, Synthesis, Structure and Biological Activity of New Five‐Membered Heterocyclic Systems Based on 2,7‐Naphthyridines: A New Class of Psychotropic Compounds
2026
·
Samvel N. Sirakanyan
, Anush A. Hovakimyan
, et al.
·
Archiv der Pharmazie
PDF
CCDC 2425218: Experimental Crystal Structure Determination
2026
·
Sirakanyan, Samvel N.
, Hakobyan, Elmira K.
, et al.
·
The Cambridge Structural Database
Synthesis, neurotropic activity and docking studies of 1,2,4-triazole-linked hybrids based on 2,7-naphthyridine and bispidine rings
2026
·
Samvel N. Sirakanyan
, Athina Geronikaki
, et al.
·
RSC Advances
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Works count:
8
Citation count:
18
H-index:
3
I10-index:
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