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Recent Advances in the Application of Barbituric Acid Derivatives in Multicomponent Reactions
Recent Advances in the Application of Barbituric Acid Derivatives in Multicomponent Reactions
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Recent Advances in the Application of Barbituric Acid Derivatives in Multicomponent Reactions

Ziarani, Ghodsi Mohammadi ; Khademi, Mahdieh ; Mohajer, Fatemeh ; Yadav, Sangeeta ; Tomar, Ravi

Current organic chemistry, 2022-01, Vol.26 (2), p.162-188 [Periódico revisado por pares]

Bentham Science Publishers

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2
Pyrimido[5,4‑d]pyrimidine-Based Compounds as a Novel Class of Antitrypanosomal and Antileishmanial Agents
Pyrimido[5,4‑d]pyrimidine-Based Compounds as a Novel Class of Antitrypanosomal and Antileishmanial Agents
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Pyrimido[5,4‑d]pyrimidine-Based Compounds as a Novel Class of Antitrypanosomal and Antileishmanial Agents

Lopes, André ; Santarém, Nuno ; Cordeiro-da-Silva, Anabela ; Carvalho, M. Alice

ACS medicinal chemistry letters, 2022-09, Vol.13 (9), p.1427-1433 [Periódico revisado por pares]

American Chemical Society

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3
Synthesis and antitumor activity of isolongifoleno[7,8‐d]thiazolo[3,2‐a]pyrimidine derivatives via enhancing ROS level
Synthesis and antitumor activity of isolongifoleno[7,8‐d]thiazolo[3,2‐a]pyrimidine derivatives via enhancing ROS level
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Synthesis and antitumor activity of isolongifoleno[7,8‐d]thiazolo[3,2‐a]pyrimidine derivatives via enhancing ROS level

Ma, Chonghui ; Wang, Yunyun ; Dong, Fuhao ; Wang, Zhonglong ; Zhao, Yuxun ; Shan, Yu ; Gu, Wen ; Wang, Shifa

Chemical biology & drug design, 2019-08, Vol.94 (2), p.1457-1466 [Periódico revisado por pares]

England

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4
Design, synthesis, and biological evaluation of thieno[3,2‐d]pyrimidine derivatives as potential simplified phosphatidylinositol 3‐kinase alpha inhibitors
Design, synthesis, and biological evaluation of thieno[3,2‐d]pyrimidine derivatives as potential simplified phosphatidylinositol 3‐kinase alpha inhibitors
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Design, synthesis, and biological evaluation of thieno[3,2‐d]pyrimidine derivatives as potential simplified phosphatidylinositol 3‐kinase alpha inhibitors

Yang, Xiuyan ; Deng, Meng ; Zhang, Xi ; Wang, Yi ; Song, Kun ; Cong, Ruan ; Meng, Linghua ; Zhang, Jian

Chemical biology & drug design, 2019-12, Vol.94 (6), p.2013-2022 [Periódico revisado por pares]

England

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5
Aggregation‐induced narrowband isomeric fluorophores for ultraviolet nondoped OLEDs by engineering multiple nonbonding interactions
Aggregation‐induced narrowband isomeric fluorophores for ultraviolet nondoped OLEDs by engineering multiple nonbonding interactions
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Aggregation‐induced narrowband isomeric fluorophores for ultraviolet nondoped OLEDs by engineering multiple nonbonding interactions

Huo, Yumiao ; Qi, Haoyuan ; He, Shuyao ; Li, Jie ; Song, Shuping ; Lv, Jichen ; Liu, Yuchao ; Peng, Ling ; Ying, Shian ; Yan, Shouke

Aggregate (Hoboken), 2023-12, Vol.4 (6), p.n/a [Periódico revisado por pares]

Wiley

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6
Multicomponent Strategy for the Preparation of Pyrrolo[1,2-a]- pyrimidine Derivatives under Catalyst-Free and Microwave Irradiation Conditions
Multicomponent Strategy for the Preparation of Pyrrolo[1,2-a]- pyrimidine Derivatives under Catalyst-Free and Microwave Irradiation Conditions
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Multicomponent Strategy for the Preparation of Pyrrolo[1,2-a]- pyrimidine Derivatives under Catalyst-Free and Microwave Irradiation Conditions

Xun, Zhan ; Feng, Xian ; Wang, Jianjun ; Shi, Daqing ; Huang, Zhibin

Chinese journal of chemistry, 2016-07, Vol.34 (7), p.696-702 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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7
A facile synthesis of the novel thiazolo[3,2-a]pyrimidine derivatives
A facile synthesis of the novel thiazolo[3,2-a]pyrimidine derivatives
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A facile synthesis of the novel thiazolo[3,2-a]pyrimidine derivatives

Studzinska, Renata ; Wroblewski, Marcin ; Karczmarska-Wodzka, Aleksandra ; Kolodziejska, Renata

Tetrahedron letters, 2014-02, Vol.55 (7), p.1384-1386 [Periódico revisado por pares]

Elsevier Ltd

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8
QSAR analysis of pyrimidine derivatives as VEGFR-2 receptor inhibitors to inhibit cancer using multiple linear regression and artificial neural network
QSAR analysis of pyrimidine derivatives as VEGFR-2 receptor inhibitors to inhibit cancer using multiple linear regression and artificial neural network
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QSAR analysis of pyrimidine derivatives as VEGFR-2 receptor inhibitors to inhibit cancer using multiple linear regression and artificial neural network

Masoomi Sefiddashti, Fariba ; Asadpour, Saeid ; Haddadi, Hedayat ; Ghanavati Nasab, Shima

Research in pharmaceutical sciences, 2021-11, Vol.16 (6), p.596-611 [Periódico revisado por pares]

Iran: Wolters Kluwer - Medknow Publications

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9
[1,2,4]Triazolo[1,5-a]pyrimidine derivative (Mol-5) is a new NS5-RdRp inhibitor of DENV2 proliferation and DENV2-induced inflammation
[1,2,4]Triazolo[1,5-a]pyrimidine derivative (Mol-5) is a new NS5-RdRp inhibitor of DENV2 proliferation and DENV2-induced inflammation
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[1,2,4]Triazolo[1,5-a]pyrimidine derivative (Mol-5) is a new NS5-RdRp inhibitor of DENV2 proliferation and DENV2-induced inflammation

Wan, Yi-Hong ; Wu, Wen-Yu ; Guo, Song-Xin ; He, Shi-Jun ; Tang, Xiao-Dong ; Wu, Xiao-Yun ; Nandakumar, Kutty Selva ; Zou, Min ; Li, Lin ; Chen, Xiao-Guang ; Liu, Shu-Wen ; Yao, Xin-Gang

Acta pharmacologica Sinica, 2020-05, Vol.41 (5), p.706-718 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Bisarylureas Based on 1H-Pyrazolo[3,4-d]pyrimidine Scaffold as Novel Pan-RAF Inhibitors with Potent Anti-Proliferative Activities: Structure-Based Design, Synthesis, Biological Evaluation and Molecular Modelling Studies
Bisarylureas Based on 1H-Pyrazolo[3,4-d]pyrimidine Scaffold as Novel Pan-RAF Inhibitors with Potent Anti-Proliferative Activities: Structure-Based Design, Synthesis, Biological Evaluation and Molecular Modelling Studies
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Bisarylureas Based on 1H-Pyrazolo[3,4-d]pyrimidine Scaffold as Novel Pan-RAF Inhibitors with Potent Anti-Proliferative Activities: Structure-Based Design, Synthesis, Biological Evaluation and Molecular Modelling Studies

Fu, Yu ; Wang, Yuanyuan ; Wan, Shanhe ; Li, Zhonghuang ; Wang, Guangfa ; Zhang, Jiajie ; Wu, Xiaoyun

Molecules (Basel, Switzerland), 2017-03, Vol.22 (4), p.542 [Periódico revisado por pares]

Switzerland: MDPI AG

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