Search Results - "Pinna, G A"

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  1. 1

    Synthesis of biologically active bridged diazabicycloheptanes by Murineddu, G, Asproni, B, Pinna, G, Curzu, M M, Dore, A, Pau, A, Deligia, F, Pinna, G A

    Published in Current medicinal chemistry (01-11-2012)
    “…The chemistry underlying how diazabicycloheptanes are assembled is described, subdivided according to chemical structure of two types, the 3,6…”
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  2. 2

    An overview on different classes of viral entry and respiratory syncitial virus (RSV) fusion inhibitors by Murineddu, G, Murruzzu, C, Pinna, G A

    Published in Current medicinal chemistry (01-04-2010)
    “…The therapeutic approach to AIDS is based on the combination of different drugs in the highly active antiretroviral therapy (HAART) regimen. These drugs have a…”
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  3. 3

    The novel cannabinoid antagonist SM-11 reduces hedonic aspect of food intake through a dopamine-dependent mechanism by Fois, G.R., Fattore, L., Murineddu, G., Salis, A., Pintore, G., Asproni, B., Pinna, G.A., Diana, M.

    Published in Pharmacological research (01-11-2016)
    “…[Display omitted] Cannabinoids, endogenous and exogenously administered, are known to positively regulate food intake and energy balance. Since CB1 receptor…”
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  4. 4

    Synthesis and aldose reductase inhibitory activities of novel thienocinnolinone derivatives by Pau, A, Asproni, B, Boatto, G, Grella, G.E, De Caprariis, P, Costantino, L, Pinna, G.A

    “…A novel series of tetrahydrothieno[2,3- h]cinnolinone derivatives were synthesized and evaluated in vitro for their ability to inhibit aldose reductase (ALR2),…”
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  5. 5

    Synthesis and cytotoxicity of substituted 2-benzylnaphth[2,3- d]imidazoles by Grella, G.E, Cabras, M.C, Murineddu, G, Pau, A, Pinna, G.A

    “…Designed as a new series of so called “bivalent ligand” containing the proposed 2-benzylnaphthimidazole-type structure, a number of 2-benzylnaphth[2,3-…”
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  6. 6

    Synthesis and Anti-HIV-1 Activity of New Delavirdine Analogues Carrying Arylpyrrole Moieties by PINNA, Gérard Aimè, LORIGA, Giovanni, MURINEDDU, Gabriele, GRELLA, Giuseppe, MURA, Massimo, VARGIU, Laura, MURGIONI, Chiara, COLLA, Paolo LA

    Published in Chemical & pharmaceutical bulletin (01-11-2001)
    “…In our search for novel anti-human immunodeficiency virus (HIV)-1 agents, 14 delavirdine analogues were synthesized and evaluated as potential anti-HIV-1…”
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  7. 7

    Adventitious buds on roots of Siphanthera arenaria (DC.) Cogn. (Melastomataceae), an annual plant from the cerrado biome by Menezes-e-Vasconcelos, K., Melo-de-Pinna, G. F. A.

    Published in Folia geobotanica (01-04-2024)
    “…Plants from Brazilian tropical grasslands of the cerrado biome (also referred to as the Cerrado region) are characterized by the possessing of belowground…”
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  8. 8
  9. 9

    Synthesis and cytotoxicity evaluation of thiophene analogues of 1-methyl-2,3-bis(hydroxymethyl)benzo[ g]indole bis[ N-(2-propyl)carbamate] by Pirisi, M.A, Murineddu, G, Mussinu, J.M, Pinna, G.A

    Published in Farmaco (Società chimica italiana : 1989) (01-04-2002)
    “…The cytotoxicity of the bis[ N-(2-propyl)carbamates] 2 and 3 which are linked to thieno[ i, j- g]indole scaffolds through methylene bridges were studied as…”
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  11. 11

    Synthesis and μ-opioid receptor affinity of a new series of nitro substituted 3,8-diazabicyclo[3.2.1]octane derivatives by Barlocco, D., Cignarella, G., Vianello, P., Villa, S., Pinna, G.A., Fadda, P., Fratta, W.

    Published in Farmaco (Società chimica italiana : 1989) (01-08-1998)
    “…A new series of analogues (1c–j; 2c–i) of the previously reported analgesic 3,8-diazabicyclo[3.2.l]octanes (1a,b; 2a,b) was synthesized and tested for their…”
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  12. 12

    Benzocondensed derivatives as rigid analogues of the μ-opioid agonist 3(8)-cinnamyl-8(3)-propionyl-3,8-diazabicyclo[3.2.1]octanes: synthesis, modeling, and affinity by Cignarella, G, Barlocco, D, Vianello, P, Villa, S, Pinna, G.A, Fadda, P, Fratta, W, Toma, L, Gessi, S

    Published in Farmaco (Società chimica italiana : 1989) (01-10-1998)
    “…A new series of rigid analogues ( 1a–g, 2a–g) of the previously reported analgesic 3-cinnamyl-8-propionyl-3,8-diazabicyclo[3.2.1]octane ( I) and its reverted…”
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  13. 13

    Synthesis and pharmacological evaluation of 4a-methyl-4,4a,5,6-tetrahydrothieno[2,3-h]cinnolin-3(2H)-ones by Pinna, G A, Salis, E, Berta, D, Gavini, E, D'Amico, M

    Published in Farmaco (Società chimica italiana : 1989) (01-01-1997)
    “…A number of 4a-methyl-4,4a,5,6-tetrahydrothieno[2,3-h]cinnolin-3(2H)-one s (3-5) have been synthesized and tested for their pharmacological profile. These were…”
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  14. 14

    Morphology and anatomy of a leaf mine in Vismia guianensis (Aubl.) Choisy (Clusiaceae) in a fragment of Brazilian Atlantic forest by Almeida-Cortez, J S, Melo-de-Pinna, G F A

    Published in Brazilian journal of biology (01-05-2006)
    “…Mines or hyponomes are channels caused by larva miners consuming internal plant tissues. These miners live on the leaf and feed from these tissues. Leaf mines…”
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  15. 15

    Synthesis, modelling, and μ-opioid receptor affinity of N-3(9)-arylpropenyl- N-9(3)-propionyl-3,9-diazabicyclo[3.3.1]nonanes by Pinna, G.A, Murineddu, G, Curzu, M.M, Villa, S, Vianello, P, Borea, P.A, Gessi, S, Toma, L, Colombo, D, Cignarella, G

    Published in Farmaco (Società chimica italiana : 1989) (01-08-2000)
    “…A series of N-3-arylpropenyl- N-9-propionyl-3,9-diazabicyclo[3.3.1]nonanes ( 1a–g) and of reverted N-3-propionyl- N-9-arylpropenyl isomers ( 2a–g), as…”
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  16. 16

    Synthesis and pharmacological evaluation of 4,4a,5,6-tetrahydro-7,8-disubstituted-benzo[h]cinnolin-3(2H)-ones by Pinna, G A, Loriga, M, Curzu, M M, D'Amico, M

    Published in Farmaco (Società chimica italiana : 1989) (01-01-1997)
    “…7,8-disubstituted-4,4a,5,6-tetrahydrobenzo[h]cinnolin-3(2H)-ones 2-4 have been synthesized and tested in comparison with the 8-acetylamino-4,4a,5,…”
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  17. 17

    Pyridazine N-oxides. II. Synthesis and in vitro antimicrobial evaluation of 3-chloro-4-carbamoyl-5-aryl-6-methyl-pyridazine N-oxides by Gavini, E, Juliano, C, Mulè, A, Pirisino, G, Pinna, G A

    Published in Farmaco (Società chimica italiana : 1989) (01-01-1997)
    “…As a part of a research project on antimicrobial agents, various novel carbamoyl derivatives of pyridazine-N-oxides 7a-j were prepared in moderate to good…”
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  18. 18

    Synthesis and pharmacological evaluation of 5,6-dihydrobenzo[f] cinnolin-2(3H)ones analogues of antihypertensive and antiaggregating benzo[h]cinnolinones by Pinna, G A, Curzu, M M, Fraghì, P, Gavini, E, D'Amico, M

    Published in Farmaco (Società chimica italiana : 1989) (01-10-1996)
    “…Two new dihydrobenzo[f]cinnolin-2(3H)ones (4a,b) have been synthesized and tested for their hypotensive, antihypertensive and antiaggregating activities in…”
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  19. 19

    Morphology and anatomy of leaf mine in Richterago riparia Roque (Asteraceae) in the campos rupestres of Serra do Cipó, Brazil by Melo De Pinna, G F A, Kraus, J E, de Menezes, N L

    Published in Brazilian journal of biology (01-02-2002)
    “…The leaf mine in Richterago riparia is caused by a lepidopteran larva (lepidopteronome). The leaves of R. riparia show campdodrome venation; the epidermis is…”
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  20. 20

    Synthesis of 1-methyl-2,3-dimethyl-N(isopropyl)carbamates-4,5-dihydro-7-R'- 8-R-1H-benzo[g]indoles and evaluation of in vitro anticancer activity by Pinna, G A, Pirisi, M A, Paglietti, G

    Published in Farmaco (Società chimica italiana : 1989) (01-02-1994)
    “…The synthesis of 7-mono or 7,8-disubstituted 4,5-dihydro-1-methyl-1H- benzo[g]indoles bearing a methyl-N-isopropylcarbamate group in position 2 or 2,3 of the…”
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