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Pyrrolo[3,2-c]pyridine derivatives as inhibitors of platelet aggregation
Altomare C., Summo L., Cellamare S., Varlamov A.V., Voskressensky L.G., Borisova T.N., Carotti A.
A series of pyrrolo[3,2-c]pyridines, isosteres of the antithrombotic drug ticlopidine, has been
Recyclization of benzofuropyridines by the action of activated alkynes in the synthesis of spiro[benzofuropyridines], representatives of a new class of acetylcholinesterase inhibitors
Voskressensky L.G., Kovaleva S.A., Borisova T.N., Eresko A.B., Tolkunov V.S., Tolkunov S.V., Listratova A.V., Altomare C., Varlamov A.V., De Candia M.
A study was carried out on the domino transformations of tetrahydrobenzofuro[2,3-c
Pyrrolo[2,1-a]isoquinoline scaffold in drug discovery: Advances in synthesis and medicinal chemistry
Matveeva M.D., Purgatorio R., Voskressensky L.G., Altomare C.D.
Synthesis of Novel Benzo[b][1,6]naphthyridine Derivatives and Investigation of Their Potential as Scaffolds of MAO Inhibitors
Kulikova Larisa N., Raesi Ghulam Reza, Levickaya Daria D., Purgatorio Rosa, Spada Gabriella La, Catto Marco, Altomare Cosimo D., Voskressensky Leonid G.
for the first time. Among the newly synthesized derivatives, 5c–h proved to be MAO B inhibitors with potency
Reductive domino reaction to access chromeno[2,3-c]isoquinoline-5-amines with antiproliferative activities against human tumor cells
Yue X., Festa A.A., Storozhenko O.A., Varlamov A.V., Subramani K., Boccarelli A., Purgatorio R., Altomare C.D., Voskressensky L.G.
and results in the formation of nineteen 12H-chromeno[2,3-c]isoquinoline-5-amine derivatives. Four new bonds
3-benzazecine-based cyclic allene derivatives as highly potent P-glycoprotein inhibitors overcoming doxorubicin multidrug resistance
Titov A.A., Niso M., Candia M., Kobzev M.S., Varlamov A.V., Borisova T.N., Voskressensky L.G., Colabufo N.A., Cellamare S., Pisani L., Altomare C.D.
Aim: Enamino 3-benzazecine compounds, incorporating the C6-C8 allene system, were synthesized
Synthesis of Isomeric 3-Benzazecines Decorated with Endocyclic Allene Moiety and Exocyclic Conjugated Double Bond and Evaluation of Their Anticholinesterase Activity
Titov A.A., Purgatorio R., Obydennik A.Y., Listratova A.V., Borisova T.N., De Candia M., Catto M., Altomare C.D., Varlamov A.V., Voskressensky L.G.
-benzazecines incorporating an endocyclic C6–C8 allene fragment and the -ylidene derivatives 6-methoxymethylene
Tandem cleavage of hydrogenated beta- and gamma-carbolines - New practical synthesis of tetrahydroazocino[4,5-b]indoles and tetrahydroazocino[5,4-b]-indoles showing acetylcholinesterase inhibitory activity
Voskressensky L.G., Borisova T.N., Kulikova L.N., Varlamov A.V., Catto M., Altomare C., Carotti A.
50 values in the micromolar range, compound 17 being the most potent (IC50 = 8.7 mum). ((C) Wiley
Advances in synthesis of novel annulated azecines and their unique pharmacological properties
Listratova A.V., Samarelli F., Titov A.A., Purgatorio R., De Candia M., Catto M., Varlamov A.V., Voskressensky L.G., Altomare C.D.
Annulated azecines, mostly partially saturated benzo[d]azecine and dibenzo[c,g]azecine fusion
Ester derivatives of annulated tetrahydroazocines: A new class of selective acetylcholinesterase inhibitors
Carotti A., Catto M., Borisova T.N., Varlamov A.V., Méndez-Álvarez E., Soto-Otero R., Voskressensky L.G., Altomare C., De Candia M.

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