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1
Estrogenic activity of constituents from the rhizomes of Rheum undulatum Linné
Estrogenic activity of constituents from the rhizomes of Rheum undulatum Linné
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Estrogenic activity of constituents from the rhizomes of Rheum undulatum Linné

Park, SeonJu ; Kim, Yun Na ; Kwak, Hee Jae ; Jeong, Eun Ju ; Kim, Seung Hyun

Bioorganic & medicinal chemistry letters, 2018-02, Vol.28 (4), p.552-557 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Tetra-aryl cyclobutane and stilbenes from the rhizomes of Rheum undulatum and their α-glucosidase inhibitory activity: Biological evaluation, kinetic analysis, and molecular docking simulation
Tetra-aryl cyclobutane and stilbenes from the rhizomes of Rheum undulatum and their α-glucosidase inhibitory activity: Biological evaluation, kinetic analysis, and molecular docking simulation
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Tetra-aryl cyclobutane and stilbenes from the rhizomes of Rheum undulatum and their α-glucosidase inhibitory activity: Biological evaluation, kinetic analysis, and molecular docking simulation

Ha, Manh Tuan ; Kim, Minji ; Kim, Chung Sub ; Park, Se-Eun ; Kim, Jeong Ah ; Woo, Mi Hee ; Choi, Jae Sue ; Min, Byung Sun

Bioorganic & medicinal chemistry letters, 2020-04, Vol.30 (8), p.127049, Article 127049 [Periódico revisado por pares]

England: Elsevier Ltd

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3
Resveratrol analogues like piceatannol are potent antioxidants as quantitatively demonstrated through the high scavenging ability against reactive oxygen species and methyl radical
Resveratrol analogues like piceatannol are potent antioxidants as quantitatively demonstrated through the high scavenging ability against reactive oxygen species and methyl radical
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Resveratrol analogues like piceatannol are potent antioxidants as quantitatively demonstrated through the high scavenging ability against reactive oxygen species and methyl radical

Sueishi, Yoshimi ; Nii, Risako ; Kakizaki, Naru

Bioorganic & medicinal chemistry letters, 2017-12, Vol.27 (23), p.5203-5206 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Induced osteoblast differentiation by amide derivatives of stilbene: The possible osteogenic agents
Induced osteoblast differentiation by amide derivatives of stilbene: The possible osteogenic agents
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Induced osteoblast differentiation by amide derivatives of stilbene: The possible osteogenic agents

Imran Ahamad, Mohd ; Prakash, Ravi ; John, Aijaz A ; Wani, Zahoor ; Yadav, Deepika ; Bawankule, Dnyaneshwar U. ; Luqman, Suaib ; Khan, Feroz ; Singh, Divya ; Gupta, Atul

Bioorganic & medicinal chemistry letters, 2020-06, Vol.30 (11), p.127138-127138, Article 127138 [Periódico revisado por pares]

England: Elsevier Ltd

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5
Synthesis and antiproliferative evaluation of 2-hydroxylated (E)-stilbenes
Synthesis and antiproliferative evaluation of 2-hydroxylated (E)-stilbenes
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Synthesis and antiproliferative evaluation of 2-hydroxylated (E)-stilbenes

Zhang, Yan ; Shen, Mingyun ; Cui, Sunliang ; Hou, Tingjun

Bioorganic & medicinal chemistry letters, 2014-12, Vol.24 (23), p.5470-5472 [Periódico revisado por pares]

England: Elsevier Ltd

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6
Synthesis and cytotoxic activity evaluation of 2,3-thiazolidin-4-one derivatives on human breast cancer cell lines
Synthesis and cytotoxic activity evaluation of 2,3-thiazolidin-4-one derivatives on human breast cancer cell lines
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Synthesis and cytotoxic activity evaluation of 2,3-thiazolidin-4-one derivatives on human breast cancer cell lines

Sala, Marina ; Chimento, Adele ; Saturnino, Carmela ; Gomez-Monterrey, Isabel M. ; Musella, Simona ; Bertamino, Alessia ; Milite, Ciro ; Sinicropi, Maria Stefania ; Caruso, Anna ; Sirianni, Rosa ; Tortorella, Paolo ; Novellino, Ettore ; Campiglia, Pietro ; Pezzi, Vincenzo

Bioorganic & medicinal chemistry letters, 2013-09, Vol.23 (17), p.4990-4995 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Synthesis and biological activity of pyrrole analogues of combretastatin A-4
Synthesis and biological activity of pyrrole analogues of combretastatin A-4
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Synthesis and biological activity of pyrrole analogues of combretastatin A-4

Jung, Eun-Kyung ; Leung, Euphemia ; Barker, David

Bioorganic & medicinal chemistry letters, 2016-07, Vol.26 (13), p.3001-3005 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Novel Aza-resveratrol analogs: Synthesis, characterization and anticancer activity against breast cancer cell lines
Novel Aza-resveratrol analogs: Synthesis, characterization and anticancer activity against breast cancer cell lines
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Novel Aza-resveratrol analogs: Synthesis, characterization and anticancer activity against breast cancer cell lines

Siddiqui, Areej ; Dandawate, Prasad ; Rub, Rukhsana ; Padhye, Subhash ; Aphale, Shama ; Moghe, Alpana ; Jagyasi, Amrit ; Venkateswara Swamy, K. ; Singh, Bhupendra ; Chatterjee, Anwesha ; Ronghe, Amruta ; Bhat, Hari K.

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (3), p.635-640 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Antiplasmodial flavanones and a stilbene from Carpha glomerata
Antiplasmodial flavanones and a stilbene from Carpha glomerata
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Antiplasmodial flavanones and a stilbene from Carpha glomerata

Cho, Namki ; Valenciano, Ana Lisa ; Du, Yongle ; Clement, Jason ; Cassera, Maria B. ; Goetz, Michael ; Kingston, David G.I.

Bioorganic & medicinal chemistry letters, 2018-11, Vol.28 (20), p.3368-3371 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Pterostilbene-O-acetamidoalkylbenzylamines derivatives as novel dual inhibitors of cholinesterase with anti-β-amyloid aggregation and antioxidant properties for the treatment of Alzheimer’s disease
Pterostilbene-O-acetamidoalkylbenzylamines derivatives as novel dual inhibitors of cholinesterase with anti-β-amyloid aggregation and antioxidant properties for the treatment of Alzheimer’s disease
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Pterostilbene-O-acetamidoalkylbenzylamines derivatives as novel dual inhibitors of cholinesterase with anti-β-amyloid aggregation and antioxidant properties for the treatment of Alzheimer’s disease

Li, Yuxing ; Qiang, Xiaoming ; Li, Yan ; Yang, Xia ; Luo, Li ; Xiao, Ganyuan ; Cao, Zhongcheng ; Tan, Zhenghuai ; Deng, Yong

Bioorganic & medicinal chemistry letters, 2016-04, Vol.26 (8), p.2035-2039 [Periódico revisado por pares]

England: Elsevier Ltd

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