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1
Native chemical ligation in protein synthesis and semi-synthesis
Native chemical ligation in protein synthesis and semi-synthesis
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Native chemical ligation in protein synthesis and semi-synthesis

Conibear, Anne C ; Watson, Emma E ; Payne, Richard J ; Becker, Christian F. W

Chemical Society reviews, 2018-12, Vol.47 (24), p.946-968 [Periódico revisado por pares]

England: Royal Society of Chemistry

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2
Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)
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Enabling chemical protein (semi)synthesis via reducible solubilizing tags (RSTs)

Liu, Jiamei ; Wei, Tongyao ; Tan, Yi ; Liu, Heng ; Li, Xuechen

Chemical science (Cambridge), 2022-02, Vol.13 (5), p.1367-1374 [Periódico revisado por pares]

England: Royal Society of Chemistry

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3
Semi-Synthesis, Cytotoxic Evaluation, and Structure-Activity Relationships of Brefeldin A Derivatives with Antileukemia Activity
Semi-Synthesis, Cytotoxic Evaluation, and Structure-Activity Relationships of Brefeldin A Derivatives with Antileukemia Activity
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Semi-Synthesis, Cytotoxic Evaluation, and Structure-Activity Relationships of Brefeldin A Derivatives with Antileukemia Activity

Lu, Xu-Xiu ; Jiang, Yao-Yao ; Wu, Yan-Wei ; Chen, Guang-Ying ; Shao, Chang-Lun ; Gu, Yu-Cheng ; Liu, Ming ; Wei, Mei-Yan

Marine drugs, 2021-12, Vol.20 (1), p.26 [Periódico revisado por pares]

Switzerland: MDPI AG

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4
Taccalonolides: Structure, semi-synthesis, and biological activity
Taccalonolides: Structure, semi-synthesis, and biological activity
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Taccalonolides: Structure, semi-synthesis, and biological activity

Li, Yan ; Du, Yu-Feng ; Gao, Feng ; Xu, Jin-Bu ; Zheng, Ling-Li ; Liu, Gang ; Lei, Yu

Frontiers in pharmacology, 2022-08, Vol.13, p.968061-968061 [Periódico revisado por pares]

Frontiers Media S.A

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5
Semi-synthesis of thioamide containing proteins
Semi-synthesis of thioamide containing proteins
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Semi-synthesis of thioamide containing proteins

Wang, Yanxin J ; Szantai-Kis, D. Miklos ; Petersson, E. James

Organic & biomolecular chemistry, 2015-05, Vol.13 (18), p.574-581 [Periódico revisado por pares]

England

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6
Semi-Synthesis of Different Pyranoflavonoid Backbones and the Neurogenic Potential
Semi-Synthesis of Different Pyranoflavonoid Backbones and the Neurogenic Potential
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Semi-Synthesis of Different Pyranoflavonoid Backbones and the Neurogenic Potential

Urmann, Corinna ; Bieler, Lara ; Hackl, Michael ; Chia-Leeson, Olivia ; Couillard-Despres, Sebastien ; Riepl, Herbert

Molecules (Basel, Switzerland), 2023-05, Vol.28 (10), p.4023 [Periódico revisado por pares]

Switzerland: MDPI AG

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7
Semi-Synthesis of N -Aryl Amide Analogs of Piperine from Piper nigrum and Evaluation of Their Antitrypanosomal, Antimalarial, and Anti-SARS-CoV-2 Main Protease Activities
Semi-Synthesis of N -Aryl Amide Analogs of Piperine from Piper nigrum and Evaluation of Their Antitrypanosomal, Antimalarial, and Anti-SARS-CoV-2 Main Protease Activities
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Semi-Synthesis of N -Aryl Amide Analogs of Piperine from Piper nigrum and Evaluation of Their Antitrypanosomal, Antimalarial, and Anti-SARS-CoV-2 Main Protease Activities

Wansri, Rattanaporn ; Lin, Aye Chan Khine ; Pengon, Jutharat ; Kamchonwongpaisan, Sumalee ; Srimongkolpithak, Nitipol ; Rattanajak, Roonglawan ; Wilasluck, Patcharin ; Deetanya, Peerapon ; Wangkanont, Kittikhun ; Hengphasatporn, Kowit ; Shigeta, Yasuteru ; Liangsakul, Jatupol ; Suroengrit, Aphinya ; Boonyasuppayakorn, Siwaporn ; Chuanasa, Taksina ; De-Eknamkul, Wanchai ; Hannongbua, Supot ; Rungrotmongkol, Thanyada ; Chamni, Supakarn

Molecules (Basel, Switzerland), 2022-04, Vol.27 (9), p.2841 [Periódico revisado por pares]

Switzerland: MDPI AG

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8
New Anticancer Theobromine Derivative Targeting EGFRWT and EGFRT790M: Design, Semi-Synthesis, In Silico, and In Vitro Anticancer Studies
New Anticancer Theobromine Derivative Targeting EGFRWT and EGFRT790M: Design, Semi-Synthesis, In Silico, and In Vitro Anticancer Studies
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New Anticancer Theobromine Derivative Targeting EGFRWT and EGFRT790M: Design, Semi-Synthesis, In Silico, and In Vitro Anticancer Studies

Elkaeed, Eslam B. ; Yousef, Reda G. ; Elkady, Hazem ; Alsfouk, Aisha A. ; Husein, Dalal Z. ; Ibrahim, Ibrahim M. ; Metwaly, Ahmed M. ; Eissa, Ibrahim H.

Molecules (Basel, Switzerland), 2022-09, Vol.27 (18), p.5859 [Periódico revisado por pares]

Basel: MDPI AG

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9
Research Advances in Clinical Applications, Anticancer Mechanism, Total Chemical Synthesis, Semi-Synthesis and Biosynthesis of Paclitaxel
Research Advances in Clinical Applications, Anticancer Mechanism, Total Chemical Synthesis, Semi-Synthesis and Biosynthesis of Paclitaxel
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Research Advances in Clinical Applications, Anticancer Mechanism, Total Chemical Synthesis, Semi-Synthesis and Biosynthesis of Paclitaxel

Zhang, Shengnan ; Ye, Taiqiang ; Liu, Yibin ; Hou, Guige ; Wang, Qibao ; Zhao, Fenglan ; Li, Feng ; Meng, Qingguo

Molecules (Basel, Switzerland), 2023-11, Vol.28 (22), p.7517 [Periódico revisado por pares]

Basel: MDPI AG

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10
Semi-Synthesis of Harringtonolide Derivatives and Their Antiproliferative Activity
Semi-Synthesis of Harringtonolide Derivatives and Their Antiproliferative Activity
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Semi-Synthesis of Harringtonolide Derivatives and Their Antiproliferative Activity

Wu, Xiutao ; Gong, Lijie ; Chen, Chen ; Tao, Ye ; Zhou, Wuxi ; Kong, Lingyi ; Luo, Jianguang

Molecules (Basel, Switzerland), 2021-03, Vol.26 (5), p.1380 [Periódico revisado por pares]

Switzerland: MDPI AG

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