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Natural Product-Derived Spirooxindole Fragments Serve as Privileged Substructures for Discovery of New Anticancer Agents

Type: Journal Paper

Author : Bin Yu; Yi-Chao Zheng; Xiao-Jing Shi; Ping-Ping Qi; Hong-Min Liu

Year: 2016

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Corrigendum to: “Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents” [J. Steroid Biochem. Mol. Biol. 141 (2014) 121–134]

Type: Journal Paper

Author : Bin Yu; Xiao-Jing Shi; Ping-Ping Qi; De-Quan Yu; Hong-Min Liu

Year: 2015

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Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents

Type: Journal Paper

Author : Bin Yu; Xiao-Jing Shi; Ping-Ping Qi; De-Quan Yu; Hong-Min Liu

Year: 2014

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Structurally novel steroidal spirooxindole by241 potently inhibits tumor growth mainly through ROS-mediated mechanisms

Type: Journal Paper

Author : Xiao-Jing Shi; Bin Yu; Jun-Wei Wang; Ping-Ping Qi; Kai Tang; Xin Huang; Hong-Min Liu

Year: 2016

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A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity

Type: Journal Paper

Author : Bin Yu; Xiao-Jing Shi; Yong-Fei Zheng; Yuan Fang; En Zhang; De-Quan Yu; Hong-Min Liu

Year: 2013

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Discovery of novel steroidal pyran–oxindole hybrids as cytotoxic agents

Type: Journal Paper

Author : Bin Yu; Ping-Ping Qi; Xiao-Jing Shi; Li-Hong Shan; De-Quan Yu; Hong-Min Liu

Year: 2014

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Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach

Type: Journal Paper

Author : Bin Yu; Ping-Ping Qi; Xiao-Jing Shi; Ruilei Huang; Hao Guo; Yi-Chao Zheng; De-Quan Yu; Hong-Min Liu

Year: 2016

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Natural Product-Derived Spirooxindole Fragments Serve as Privileged Substructures for Discovery of New Anticancer Agents

Corrigendum to: “Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents” [J. Steroid Biochem. Mol. Biol. 141 (2014) 121–134]

Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents

Structurally novel steroidal spirooxindole by241 potently inhibits tumor growth mainly through ROS-mediated mechanisms

A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity

Discovery of novel steroidal pyran–oxindole hybrids as cytotoxic agents

Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach

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Natural Product-Derived Spirooxindole Fragments Serve as Privileged Substructures for Discovery of New Anticancer Agents

Corrigendum to: “Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents” [J. Steroid Biochem. Mol. Biol. 141 (2014) 121–134]

Design, synthesis and biological evaluation of novel steroidal spiro-oxindoles as potent antiproliferative agents

Structurally novel steroidal spirooxindole by241 potently inhibits tumor growth mainly through ROS-mediated mechanisms

A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity

Discovery of novel steroidal pyran–oxindole hybrids as cytotoxic agents

Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach