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Haishan Wang

Showing results (21-30 of 36) with videos related to

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Journal of Natural Products|May 25, 2002
Isolation of streptonigrin and its novel derivative from Micromonospora as inducing agents of p53-dependent cell apoptosisHaishan Wang, Su Ling Yeo, Jin Xu, et al.
Journal of Chemical Information and Modeling|October 16, 2014
Structure and ligand-based design of mTOR and PI3-kinase inhibitors leading to the clinical candidates VS-5584 (SB2343) and SB2602Anders Poulsen, Harish Nagaraj, Angeline Lee, et al.
Journal of Molecular Modeling|July 24, 2012
Structure-based design of nitrogen-linked macrocyclic kinase inhibitors leading to the clinical candidate SB1317/TG02, a potent inhibitor of cyclin dependant kinases (CDKs), Janus kinase 2 (JAK2), and Fms-like tyrosine kinase-3 (FLT3)Anders Poulsen, Anthony William, Stéphanie Blanchard, et al.
Journal of Biomolecular Screening|November 14, 2006
SIRT1 modulating compounds from high-throughput screening as anti-inflammatory and insulin-sensitizing agentsVasantha M Nayagam, Xukun Wang, Yong Cheng Tan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 30, 2011
Preclinical metabolism and disposition of SB939 (Pracinostat), an orally active histone deacetylase inhibitor, and prediction of human pharmacokineticsRamesh Jayaraman, Venkatesh Pilla Reddy, Mohammed Khalid Pasha, et al.
Fish Physiology and Biochemistry|February 17, 2020
Sugar transporter genes in grass carp (Ctenopharyngodon idellus): molecular cloning, characterization, and expression in response to different stocking densitiesXiao Liang, Fengying Yan, Yu Gao, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|January 11, 2017
Editor's Highlight: Transgenic Zebrafish Reporter Lines as Alternative In Vivo Organ Toxicity ModelsKar Lai Poon, Xingang Wang, Serene G P Lee, et al.
Bioorganic & Medicinal Chemistry Letters|May 11, 2010
Acylurea connected straight chain hydroxamates as novel histone deacetylase inhibitors: Synthesis, SAR, and in vivo antitumor activityHaishan Wang, Ze-Yi Lim, Yan Zhou, et al.
Bioorganic & Medicinal Chemistry Letters|March 23, 2012
2-anilino-4-aryl-8H-purine derivatives as inhibitors of PDK1Stéphanie Blanchard, Chang Kai Soh, Chai Ping Lee, et al.
Molecular Cancer Therapeutics|March 4, 2010
SB939, a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancerVeronica Novotny-Diermayr, Kanda Sangthongpitag, Chang Yong Hu, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Natural Products|May 25, 2002
Isolation of streptonigrin and its novel derivative from Micromonospora as inducing agents of p53-dependent cell apoptosisHaishan Wang, Su Ling Yeo, Jin Xu, et al.
Journal of Chemical Information and Modeling|October 16, 2014
Structure and ligand-based design of mTOR and PI3-kinase inhibitors leading to the clinical candidates VS-5584 (SB2343) and SB2602Anders Poulsen, Harish Nagaraj, Angeline Lee, et al.
Journal of Molecular Modeling|July 24, 2012
Structure-based design of nitrogen-linked macrocyclic kinase inhibitors leading to the clinical candidate SB1317/TG02, a potent inhibitor of cyclin dependant kinases (CDKs), Janus kinase 2 (JAK2), and Fms-like tyrosine kinase-3 (FLT3)Anders Poulsen, Anthony William, Stéphanie Blanchard, et al.
Journal of Biomolecular Screening|November 14, 2006
SIRT1 modulating compounds from high-throughput screening as anti-inflammatory and insulin-sensitizing agentsVasantha M Nayagam, Xukun Wang, Yong Cheng Tan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 30, 2011
Preclinical metabolism and disposition of SB939 (Pracinostat), an orally active histone deacetylase inhibitor, and prediction of human pharmacokineticsRamesh Jayaraman, Venkatesh Pilla Reddy, Mohammed Khalid Pasha, et al.
Fish Physiology and Biochemistry|February 17, 2020
Sugar transporter genes in grass carp (Ctenopharyngodon idellus): molecular cloning, characterization, and expression in response to different stocking densitiesXiao Liang, Fengying Yan, Yu Gao, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|January 11, 2017
Editor's Highlight: Transgenic Zebrafish Reporter Lines as Alternative In Vivo Organ Toxicity ModelsKar Lai Poon, Xingang Wang, Serene G P Lee, et al.
Bioorganic & Medicinal Chemistry Letters|May 11, 2010
Acylurea connected straight chain hydroxamates as novel histone deacetylase inhibitors: Synthesis, SAR, and in vivo antitumor activityHaishan Wang, Ze-Yi Lim, Yan Zhou, et al.
Bioorganic & Medicinal Chemistry Letters|March 23, 2012
2-anilino-4-aryl-8H-purine derivatives as inhibitors of PDK1Stéphanie Blanchard, Chang Kai Soh, Chai Ping Lee, et al.
Molecular Cancer Therapeutics|March 4, 2010
SB939, a novel potent and orally active histone deacetylase inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancerVeronica Novotny-Diermayr, Kanda Sangthongpitag, Chang Yong Hu, et al.
Pageof 4