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11
Design, synthesis and antiproliferative activity of novel heterobivalent hybrids based on imidazo[2,1-b][1,3,4]thiadiazole and imidazo[2,1-b][1,3]thiazole scaffolds
Design, synthesis and antiproliferative activity of novel heterobivalent hybrids based on imidazo[2,1-b][1,3,4]thiadiazole and imidazo[2,1-b][1,3]thiazole scaffolds
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Design, synthesis and antiproliferative activity of novel heterobivalent hybrids based on imidazo[2,1-b][1,3,4]thiadiazole and imidazo[2,1-b][1,3]thiazole scaffolds

Romagnoli, Romeo ; Baraldi, Pier Giovanni ; Prencipe, Filippo ; Balzarini, Jan ; Liekens, Sandra ; Estévez, Francisco

European journal of medicinal chemistry, 2015-08, Vol.101, p.205-217 [Periódico revisado por pares]

France: Elsevier Masson SAS

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12
Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells
Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells
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Synthesis and structure-activity relationship studies of novel 3,9-substituted α-carboline derivatives with high cytotoxic activity against colorectal cancer cells

Lin, Yi-Chien ; Chen, Yi-Fong ; Tseng, Li-Shin ; Lee, Yueh-Hsuan ; Morris-Natschke, Susan L. ; Kuo, Sheng-Chu ; Yang, Ning-Sun ; Lee, Kuo-Hsiung ; Huang, Li-Jiau

European journal of medicinal chemistry, 2016-03, Vol.110, p.98-114 [Periódico revisado por pares]

France: Elsevier Masson SAS

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13
New mixed-ligand Ni(II) and Zn(II) macrocyclic complexes with bridged (endo,endo)-bicyclo [2.2.1]hept-5-ene-2,3-dicarboxylate: Synthesis, characterization, antimicrobial and cytotoxic activity
New mixed-ligand Ni(II) and Zn(II) macrocyclic complexes with bridged (endo,endo)-bicyclo [2.2.1]hept-5-ene-2,3-dicarboxylate: Synthesis, characterization, antimicrobial and cytotoxic activity
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New mixed-ligand Ni(II) and Zn(II) macrocyclic complexes with bridged (endo,endo)-bicyclo [2.2.1]hept-5-ene-2,3-dicarboxylate: Synthesis, characterization, antimicrobial and cytotoxic activity

Antonijevic-Nikolic, Mirjana ; Drazic, Branka ; Antic-Stankovic, Jelena ; Tanaskovic, Sladjana

Journal of the Serbian Chemical Society, 2019, Vol.84 (9), p.961-973 [Periódico revisado por pares]

Serbian Chemical Society

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14
Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione
Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione
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Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione

Romagnoli, Romeo ; Baraldi, Pier Giovanni ; Salvador, Maria Kimatrai ; Camacho, M. Encarnacion ; Balzarini, Jan ; Bermejo, Jaime ; Estévez, Francisco

European journal of medicinal chemistry, 2013-05, Vol.63, p.544-557 [Periódico revisado por pares]

France: Elsevier Masson SAS

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15
Synthesis and antiproliferative evaluation of novel 8-cyclopentyl-7,8-dihydropteridin-6(5H)-one derivatives as potential anticancer agents
Synthesis and antiproliferative evaluation of novel 8-cyclopentyl-7,8-dihydropteridin-6(5H)-one derivatives as potential anticancer agents
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Synthesis and antiproliferative evaluation of novel 8-cyclopentyl-7,8-dihydropteridin-6(5H)-one derivatives as potential anticancer agents

Li, Qiu ; Jian, Xie-Er ; Ma, Yu-Feng ; Chen, Lin ; Huo, Xian-Sen ; Wang, Yu ; He, Ren-Xin ; You, Wen-Wei ; Zhao, Pei-Liang

Bioorganic & medicinal chemistry letters, 2021-01, Vol.31, p.127684-127684, Article 127684 [Periódico revisado por pares]

England: Elsevier Ltd

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16
Comparison of bioactive compounds, antioxidant and antiproliferative activities of Mon Thong durian during ripening
Comparison of bioactive compounds, antioxidant and antiproliferative activities of Mon Thong durian during ripening
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Comparison of bioactive compounds, antioxidant and antiproliferative activities of Mon Thong durian during ripening

Haruenkit, Ratiporn ; Poovarodom, Sumitra ; Vearasilp, Suchada ; Namiesnik, Jacek ; Sliwka-Kaszynska, Magda ; Park, Yong-Seo ; Heo, Buk-Gu ; Cho, Ja-Yong ; Jang, Hong Gi ; Gorinstein, Shela

Food chemistry, 2010-02, Vol.118 (3), p.540-547 [Periódico revisado por pares]

Elsevier Ltd

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17
Peruranolides A-D, four new withanolides with potential antibacterial and cytotoxic activity from Physalis peruviana L
Peruranolides A-D, four new withanolides with potential antibacterial and cytotoxic activity from Physalis peruviana L
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Peruranolides A-D, four new withanolides with potential antibacterial and cytotoxic activity from Physalis peruviana L

Li, Qian-Ran ; Liang, Hui-Jun ; Li, Bai-Lin ; Yuan, Jie ; Ao, Zhuo-Yi ; Fan, Yu-Wen ; Zhang, Wei-Jie ; Lian, Xin ; Chen, Jia-Yan ; Wang, Jian-Zhong ; Wu, Jie-Wei

Frontiers in bioscience (Landmark. Print), 2022-03, Vol.27 (3), p.98-98 [Periódico revisado por pares]

Singapore: IMR Press

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18
Diaryl-substituted benzimidazole derivatives as antiproliferative agents: Design, synthesis, in vitro activity, and SAR analysis
Diaryl-substituted benzimidazole derivatives as antiproliferative agents: Design, synthesis, in vitro activity, and SAR analysis
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Diaryl-substituted benzimidazole derivatives as antiproliferative agents: Design, synthesis, in vitro activity, and SAR analysis

Gursoy, Sule ; Ersan, Ronak Haj

Journal of molecular structure, 2024-07, Vol.1308, Article 137960 [Periódico revisado por pares]

Elsevier B.V

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19
Synthesis and Biological Evaluation of (N‐(3‐methoxyphenyl)‐4‐((aryl‐1H‐1,2,3‐triazol‐4‐yl)methyl)thiomorpholine‐2‐carboxamide 1,1‐Dioxide Hybrids as Antiproliferative Agents
Synthesis and Biological Evaluation of (N‐(3‐methoxyphenyl)‐4‐((aryl‐1H‐1,2,3‐triazol‐4‐yl)methyl)thiomorpholine‐2‐carboxamide 1,1‐Dioxide Hybrids as Antiproliferative Agents
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Synthesis and Biological Evaluation of (N‐(3‐methoxyphenyl)‐4‐((aryl‐1H‐1,2,3‐triazol‐4‐yl)methyl)thiomorpholine‐2‐carboxamide 1,1‐Dioxide Hybrids as Antiproliferative Agents

Battula, Kumara Swamy ; Narsimha, Sirassu ; Thatipamula, Ranjith Kumar ; Reddy, Yellu Narsimha ; Nagavelli, Vasudeva Reddy

ChemistrySelect (Weinheim), 2017-10, Vol.2 (29), p.9595-9598 [Periódico revisado por pares]

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20
Design, synthesis and in vitro evaluation against human cancer cells of 5-methyl-5-styryl-2,5-dihydrofuran-2-ones, a new series of goniothalamin analogues
Design, synthesis and in vitro evaluation against human cancer cells of 5-methyl-5-styryl-2,5-dihydrofuran-2-ones, a new series of goniothalamin analogues
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Design, synthesis and in vitro evaluation against human cancer cells of 5-methyl-5-styryl-2,5-dihydrofuran-2-ones, a new series of goniothalamin analogues

Bruder, Marjorie ; Vendramini-Costa, Débora Barbosa ; de Carvalho, João Ernesto ; Pilli, Ronaldo Aloise

Bioorganic & medicinal chemistry, 2013-09, Vol.21 (17), p.5107-5117 [Periódico revisado por pares]

England: Elsevier Ltd

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Deste Autor:

  1. Vieira, T
  2. Squarisi, I
  3. Alencar, S
  4. Silva, G
  5. Silva Júnior, W

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Antiproliferative Activity
  4. Humans
  5. Chemistry

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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