| Nome |
# |
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Dichloro-phenyl-benzotriazoles: a new selective class of human respiratory syncytial virus entry inhibitors, file e2f56ed7-fc56-3eaf-e053-3a05fe0a5d97
|
622
|
|
5,6-Dichloro-2-phenyl-benzotriazoles: New potent inhibitors of orthohantavirus, file e2f56ed9-13f5-3eaf-e053-3a05fe0a5d97
|
312
|
|
Design, synthesis, antiviral evaluation, and SAR studies of new 1-(phenylsulfonyl)-1H-pyrazol -4-yl-methylaniline derivatives., file e2f56ed8-471f-3eaf-e053-3a05fe0a5d97
|
228
|
|
Benzimidazole-based derivatives as privileged scaffold developed for the treatment of the RSV infection: a computational study exploring the potency and cytotoxicity profiles, file e2f56ed6-649a-3eaf-e053-3a05fe0a5d97
|
181
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|
Synthesis and in vitro antiproliferative activity of new benzothiazole derivatives, file e2f56ed3-82fc-3eaf-e053-3a05fe0a5d97
|
163
|
|
Synthesis and biological evaluation of new 3-phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones, file e2f56ed3-afc8-3eaf-e053-3a05fe0a5d97
|
110
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|
Synthesis and evaluation of in vitro biological activity of 4-substituted arylpiperazine derivatives of 1,7,8,9-tetrachloro-10,10-dimethoxy-4-azatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione, file e2f56ed3-a684-3eaf-e053-3a05fe0a5d97
|
86
|
|
Anti-BVDV activity evaluation of naphthoimidazole derivatives compared with parental imidazoquinoline compounds., file e2f56ed9-e1f2-3eaf-e053-3a05fe0a5d97
|
77
|
|
Antiviral activity of benzotriazole based derivatives, file e2f56ed9-de0c-3eaf-e053-3a05fe0a5d97
|
52
|
|
Synthesis, Antitumor and Antiviral In Vitro Activities of New Benzotriazole-Dicarboxamide Derivatives, file e2f56eda-622e-3eaf-e053-3a05fe0a5d97
|
17
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Benzimidazole-2-Phenyl-Carboxamides as Dual-Target Inhibitors of BVDV Entry and Replication, file 463d4b09-2bad-452e-9b18-272448591e66
|
16
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|
Inhibition of enterovirus a71 by a novel 2-phenyl-benzimidazole derivative, file e2f56eda-91d5-3eaf-e053-3a05fe0a5d97
|
16
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Synthesis and antiviral evaluation of 1-[(2-Phenoxyethyl)oxymethyl] and 6-(3,5-Dimethoxybenzyl) analogues of HIV drugs emivirine and TNK-651, file e2f56ed4-f8d3-3eaf-e053-3a05fe0a5d97
|
12
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N-((1,3-Diphenyl-1H-pyrazol-4-yl)methyl)anilines: A novel class of anti-RSV agents, file e2f56ed3-ba00-3eaf-e053-3a05fe0a5d97
|
11
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Facile synthesis of the NNRTI microbicide MC-1220 and synthesis of its phosphoramidate prodrugs, file e2f56ed4-bc65-3eaf-e053-3a05fe0a5d97
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11
|
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Synthesis and antiviral activity of new phenylimidazopyridines and N-benzylidenequinolinamines derived by molecular simplification of phenylimidazo[4,5-g]quinolines, file e2f56ed3-c70b-3eaf-e053-3a05fe0a5d97
|
10
|
|
null, file e2f56ed3-9ae1-3eaf-e053-3a05fe0a5d97
|
9
|
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Antiviral activity of benzimidazole derivatives. III. Novel anti-CVB-5, anti-RSV and anti-Sb-1 agents, file e2f56ed3-c13a-3eaf-e053-3a05fe0a5d97
|
9
|
|
Benzimidazole derivatives endowed with potent antileishmanial activity, file e2f56ed7-784a-3eaf-e053-3a05fe0a5d97
|
9
|
|
Antiviral activity of benzotriazole derivatives. 5-[4-(Benzotriazol-2-yl)phenoxy]-2,2-dimethylpentanoic acids potently and selectively inhibit Coxsackie Virus B5, file e2f56ed4-bc6b-3eaf-e053-3a05fe0a5d97
|
8
|
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A combined in silico/in vitro approach unveils common molecular requirements for efficient BVDV RdRp binding of linear aromatic N-polycyclic systems, file e2f56ed4-f8c8-3eaf-e053-3a05fe0a5d97
|
8
|
|
Antiviral activities of 5-chlorobenzotriazole derivatives, file e2f56ed7-9159-3eaf-e053-3a05fe0a5d97
|
8
|
|
Synthesis, cytotoxicity and antiviral evaluation of new series of imidazo[4,5-g]quinoline and pyrido[2,3-g]quinoxalinone derivatives, file e2f56ed4-a3db-3eaf-e053-3a05fe0a5d97
|
7
|
|
Synthesis and in vitro anti-HIV activity of N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives using MTT method, file e2f56ed3-7a13-3eaf-e053-3a05fe0a5d97
|
6
|
|
Synthesis of novel fluoro analogues of MKC442 as microbicides, file e2f56ed3-a1fb-3eaf-e053-3a05fe0a5d97
|
6
|
|
Biological evaluation of novel 1,4-dithiine derivatives as potential antimicrobial agents, file e2f56ed3-bfda-3eaf-e053-3a05fe0a5d97
|
6
|
|
Inhibitors of Yellow Fever Virus replication based on 1,3,5-triphenyl-4,5-dihydropyrazole scaffold: Design, synthesis and antiviral evaluation., file e2f56ed6-f01b-3eaf-e053-3a05fe0a5d97
|
6
|
|
Synthesis and biological evaluation of (acyl)hydrazones and thiosemicarbazones obtained via in situ condensation of iminium salts with nitrogen-containing nucleophiles., file e2f56ed4-4a43-3eaf-e053-3a05fe0a5d97
|
5
|
|
Synthesis and anti-HIV-1 evaluation of some novel MC-1220 analogs as non-nucleoside reverse transcriptase inhibitors, file e2f56ed4-f871-3eaf-e053-3a05fe0a5d97
|
5
|
|
Activity of bis(7-hydroxycoumarin) Mannich bases against bovine viral diarrhoea virus, file e2f56ed5-6bfd-3eaf-e053-3a05fe0a5d97
|
5
|
|
3-Aryl-2-[1H-benzotriazol-1-yl]acrylonitriles: a novel class of potent tubulin inhibitors, file e2f56ed3-79b4-3eaf-e053-3a05fe0a5d97
|
4
|
|
Syntheses and in vitro biologic screening 3 of 1-aryl-10H-[1,2,4]triazolo[30,40:3,4][1,2,4]triazino[5,6-b]indoles, file e2f56ed3-8b70-3eaf-e053-3a05fe0a5d97
|
4
|
|
Synergistic experimental/computational studies on arylazoenamine derivatives that target the bovine viral diarrhea virus RNA-dependent RNA polymerase, file e2f56ed3-9e2d-3eaf-e053-3a05fe0a5d97
|
4
|
|
Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivatives, file e2f56ed3-aaae-3eaf-e053-3a05fe0a5d97
|
4
|
|
Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 50-a-hydroxyphosphonates, file e2f56ed3-acde-3eaf-e053-3a05fe0a5d97
|
4
|
|
Synthesis, biological evaluation and binding mode of novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitro imidazoles targeted at the HIV-1 reverse transcriptase, file e2f56ed3-b8a8-3eaf-e053-3a05fe0a5d97
|
4
|
|
Unconventional Knoevenagel-type indoles: Synthesis and cell-based studies for the identification of pro-apoptotic agents, file e2f56ed4-993c-3eaf-e053-3a05fe0a5d97
|
4
|
|
Quinoxaline derivatives as new inhibitors of coxsackievirus B5, file e2f56ed7-11a9-3eaf-e053-3a05fe0a5d97
|
4
|
|
Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agents, file e2f56ed3-8ee5-3eaf-e053-3a05fe0a5d97
|
3
|
|
Antiviral activity of benzimidazole derivatives. II. Antiviral activity of 2-phenylbenzimidazole derivatives, file e2f56ed3-9b15-3eaf-e053-3a05fe0a5d97
|
3
|
|
Topical nonnucleoside reverse transcriptase inhibitor MC 1220 partially prevents vaginal RT-SHIV infection of macaques, file e2f56ed5-5f75-3eaf-e053-3a05fe0a5d97
|
3
|
|
9-Aminoacridine-based agents impair the bovine viral diarrhea virus (BVDV) replication targeting the RNA-dependent RNA polymerase (RdRp), file e2f56ed7-79d0-3eaf-e053-3a05fe0a5d97
|
3
|
|
Design, synthesis, and antiviral activities of new benzotriazole-based derivatives, file 07377711-ac49-4672-aa30-0ebb93014c0f
|
2
|
|
Synthesis and anti-HIV-1 activity of new fluoro-HEPT analogues: an investigation on fluoro versus hydroxy substituents, file e2f56ed3-79ec-3eaf-e053-3a05fe0a5d97
|
2
|
|
2,3-dihydro-1,2-diphenyl-substituted 4H-pyridinone derivatives as new anti flaviviridae inhibitors, file e2f56ed3-79f4-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-7f47-3eaf-e053-3a05fe0a5d97
|
2
|
|
Synthesis, in vitro antiproliferative and anti-HIV activity of new derivatives of 2-Piperazino-1,3-benzo[d]thiazoles, file e2f56ed3-7fad-3eaf-e053-3a05fe0a5d97
|
2
|
|
A novel synthetic route for the anti-HIV drug MC-1220 and its analogues, file e2f56ed3-8027-3eaf-e053-3a05fe0a5d97
|
2
|
|
Prompt lithiation of 1-dimethylsulfamoylthymine used for the synthesis of 1-allyloxymethyl-6-(a,2,6-trifluorobenzyl)thymine, file e2f56ed3-816d-3eaf-e053-3a05fe0a5d97
|
2
|
|
Pharmacophore modeling, resistant mutant isolation, docking, and MM-PBSA analysis: Combined experimental/computer-assisted approaches to identify new inhibitors of the bovine viral diarrhea virus (BVDV), file e2f56ed3-8242-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-825b-3eaf-e053-3a05fe0a5d97
|
2
|
|
Platinum and palladium-triazole complexes as highly potential antitumor agents, file e2f56ed3-82d6-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-82dc-3eaf-e053-3a05fe0a5d97
|
2
|
|
Protective properties of non-nucleoside reverse transcriptase inhibitor (MC1220) incorporated into liposome against intravaginal challenge of Rhesus Macaques with RT-SHIV, file e2f56ed3-82f9-3eaf-e053-3a05fe0a5d97
|
2
|
|
Synthesis and in vitro antiproliferative activity of new adamantylthiazolyl-1,3,4-oxadiazoles, file e2f56ed3-830c-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-8825-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-9f5f-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-9f61-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-9f64-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-a9d6-3eaf-e053-3a05fe0a5d97
|
2
|
|
Styrylbenzimidazoles. Synthesis and biological activity - part 3, file e2f56ed3-a9fa-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-aa74-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-ae33-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-b083-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-b0ae-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-b1dd-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-b8a1-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-b9ba-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-ba3d-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-bb39-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-bbea-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-c5fa-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-c78c-3eaf-e053-3a05fe0a5d97
|
2
|
|
Synthesis and antiproliferative acticity of basic thioanalogues of merbarone, file e2f56ed3-c8c4-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed5-53b0-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed5-59a8-3eaf-e053-3a05fe0a5d97
|
2
|
|
Antitubercular activity of quinolizidinyl/pyrrolizidinylalkyliminophenazines., file e2f56ed5-5cd6-3eaf-e053-3a05fe0a5d97
|
2
|
|
Antimicrobial activity of 10-(diphenylmethylene)-4-azatricyclo[5.2.1.0 2,6]dec-8-ene-3,5-dione derivatives, file e2f56ed5-6203-3eaf-e053-3a05fe0a5d97
|
2
|
|
Host dihydrofolate reductase (DHFR)-directed cycloguanil analogues endowed with activity against influenza virus and respiratory
syncytial virus, file e2f56ed6-7cd4-3eaf-e053-3a05fe0a5d97
|
2
|
|
Synthesis, structural characterization and biological evaluation of 4'-C-methyl- and phenyl-dioxolane pyrimidine and purine nucleosides, file e2f56ed6-efe9-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed3-7caf-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7d3f-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7d40-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7d44-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7d45-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7d46-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7e46-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7e47-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7e4d-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7ed0-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7f10-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7f2b-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-7f48-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-802e-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-8056-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-81ac-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-8239-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-827e-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-831d-3eaf-e053-3a05fe0a5d97
|
1
|
|
null, file e2f56ed3-836b-3eaf-e053-3a05fe0a5d97
|
1
|
| Totale |
2.161 |