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Refinado por: Nome da Publicação: Bioorganic & Medicinal Chemistry Letters remover assunto: Molecular Medicine remover Chemistry, Organic remover
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1
Preparation and antioxidant study of silver nanoparticles of Microsorum pteropus methanol extract
Preparation and antioxidant study of silver nanoparticles of Microsorum pteropus methanol extract
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Preparation and antioxidant study of silver nanoparticles of Microsorum pteropus methanol extract

Chick, Christian Nanga ; Misawa-Suzuki, Tomoyo ; Suzuki, Yumiko ; Usuki, Toyonobu

Bioorganic & medicinal chemistry letters, 2020-11, Vol.30 (22), p.127526-127526, Article 127526 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Design, synthesis and biological evaluation of potent EGFR kinase inhibitors against 19D/T790M/C797S mutation
Design, synthesis and biological evaluation of potent EGFR kinase inhibitors against 19D/T790M/C797S mutation
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Design, synthesis and biological evaluation of potent EGFR kinase inhibitors against 19D/T790M/C797S mutation

Su, Zhicheng ; Yang, Tingyuan ; Wang, Jie ; Lai, Mengzhen ; Tong, Linjiang ; Wumaier, Gulinuer ; Chen, Zhuo ; Li, Shengqing ; Li, Honglin ; Xie, Hua ; Zhao, Zhenjiang

Bioorganic & medicinal chemistry letters, 2020-08, Vol.30 (16), p.127327-127327, Article 127327 [Periódico revisado por pares]

Elsevier Ltd

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3
Synthesis of mitochondria-targeted coumarin-3-carboxamide fluorescent derivatives: Inhibiting mitochondrial TrxR2 and cell proliferation on breast cancer cells
Synthesis of mitochondria-targeted coumarin-3-carboxamide fluorescent derivatives: Inhibiting mitochondrial TrxR2 and cell proliferation on breast cancer cells
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Synthesis of mitochondria-targeted coumarin-3-carboxamide fluorescent derivatives: Inhibiting mitochondrial TrxR2 and cell proliferation on breast cancer cells

Li, Yuanyuan ; Tang, Qun ; Xie, Yu ; He, Dian ; Yang, Kun ; Zheng, Lifang

Bioorganic & medicinal chemistry letters, 2021-02, Vol.33, p.127750-127750, Article 127750 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Discovery of benzo[d]oxazol-2(3H)-one derivatives as a new class of TNIK inhibitors for the treatment of colorectal cancer
Discovery of benzo[d]oxazol-2(3H)-one derivatives as a new class of TNIK inhibitors for the treatment of colorectal cancer
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Discovery of benzo[d]oxazol-2(3H)-one derivatives as a new class of TNIK inhibitors for the treatment of colorectal cancer

Luo, Xinling ; Yang, Ruicheng ; Li, Yueshan ; Zhang, Liting ; Yang, Shengyong ; Li, Linli

Bioorganic & medicinal chemistry letters, 2022-07, Vol.67, p.128745-128745, Article 128745 [Periódico revisado por pares]

England: Elsevier Ltd

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5
Design, synthesis and activity evaluation of Hedgehog inhibitor Itraconazole derivatives in A549 cells
Design, synthesis and activity evaluation of Hedgehog inhibitor Itraconazole derivatives in A549 cells
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Design, synthesis and activity evaluation of Hedgehog inhibitor Itraconazole derivatives in A549 cells

Cai, Jin ; Chen, Xixi ; You, Haoyuan ; Li, Xiaojing ; Ji, Min

Bioorganic & medicinal chemistry letters, 2022-11, Vol.76, p.129011-129011, Article 129011 [Periódico revisado por pares]

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6
Isolation, structure identification and hepatoprotective activity of a polysaccharide from Sabia parviflora
Isolation, structure identification and hepatoprotective activity of a polysaccharide from Sabia parviflora
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Isolation, structure identification and hepatoprotective activity of a polysaccharide from Sabia parviflora

Zhang, Xue-Xue ; Li, Jian-Qiao ; Li, Man-Shu ; Chen, Yu ; He, Hai-Bo ; Liu, Shi-Ping ; Cheng, Fan ; Liu, Cheng-Xiong ; Zou, Kun

Bioorganic & medicinal chemistry letters, 2021-01, Vol.32, p.127719-127719, Article 127719 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Essential structure of orexin 1 receptor antagonist YNT-707: Conversion of the 16-cyclopropylmethyl group to the 16-sulfonamide group in d-nor-nalfurafine derivatives
Essential structure of orexin 1 receptor antagonist YNT-707: Conversion of the 16-cyclopropylmethyl group to the 16-sulfonamide group in d-nor-nalfurafine derivatives
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Essential structure of orexin 1 receptor antagonist YNT-707: Conversion of the 16-cyclopropylmethyl group to the 16-sulfonamide group in d-nor-nalfurafine derivatives

Katoh, Koki ; Kutsumura, Noriki ; Yamamoto, Naoshi ; Nagumo, Yasuyuki ; Saitoh, Tsuyoshi ; Ishikawa, Yukiko ; Irukayama-Tomobe, Yoko ; Tanimura, Ryuji ; Yanagisawa, Masashi ; Nagase, Hiroshi

Bioorganic & medicinal chemistry letters, 2022-03, Vol.59, p.128550-128550, Article 128550 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Preparation of a multifunctional photoactivated prodrug on a streptavidin scaffold bearing a DNA aptamer
Preparation of a multifunctional photoactivated prodrug on a streptavidin scaffold bearing a DNA aptamer
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Preparation of a multifunctional photoactivated prodrug on a streptavidin scaffold bearing a DNA aptamer

Motohashi, Yuto ; Nishihara, Tatsuya ; Tanabe, Kazuhito

Bioorganic & medicinal chemistry letters, 2022-09, Vol.71, p.128819-128819, Article 128819 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Asymmetric oxidative coupling of hydroxycarbazoles: Facile synthesis of (+)-bi-2-hydroxy-3-methylcarbazole
Asymmetric oxidative coupling of hydroxycarbazoles: Facile synthesis of (+)-bi-2-hydroxy-3-methylcarbazole
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Asymmetric oxidative coupling of hydroxycarbazoles: Facile synthesis of (+)-bi-2-hydroxy-3-methylcarbazole

Sako, Makoto ; Sugizaki, Akimasa ; Takizawa, Shinobu

Bioorganic & medicinal chemistry letters, 2018-09, Vol.28 (16), p.2751-2753 [Periódico revisado por pares]

England: Elsevier Ltd

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10
A head-to-head comparison of the inhibitory activities of 15 peptidomimetic SARS-CoV-2 3CLpro inhibitors
A head-to-head comparison of the inhibitory activities of 15 peptidomimetic SARS-CoV-2 3CLpro inhibitors
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A head-to-head comparison of the inhibitory activities of 15 peptidomimetic SARS-CoV-2 3CLpro inhibitors

Vankadara, Subramanyam ; Wong, Yun Xuan ; Liu, Boping ; See, Yi Yang ; Tan, Li Hong ; Tan, Qian Wen ; Wang, Gang ; Karuna, Ratna ; Guo, Xue ; Tan, Shu Ting ; Fong, Jia Yi ; Joy, Joma ; Chia, C.S. Brian

Bioorganic & medicinal chemistry letters, 2021-09, Vol.48, p.128263-128263, Article 128263 [Periódico revisado por pares]

England: Elsevier Ltd

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