Suchergebnisse - "Yeh, Teng-Kuang"

PubPharm (209)

81

Discovery, structure-activity relationship studies, and anti-nociceptive effects of N-(1,2,3,4-tetrahydro-1-isoquinolinylmethyl)benzamides as novel opioid receptor agonists

enthalten in: European journal of medicinal chemistry | 2016

von Chen, S. | Ke, Y. | Yeh, T. | +13

82

Activation of delta-opioid receptor contributes to the antinociceptive effect of oxycodone in mice

enthalten in: Pharmacological research | 2016

von Yang, P. | Yeh, G. | Yeh, T. | +4

83

Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual Screening

enthalten in: Journal of medicinal chemistry | 2015

von Wu, J. | Lin, S. | Liao, F. | +17

84

Novel Nrf2/ARE activator, trans-Coniferylaldehyde, induces a HO-1-mediated defense mechanism through a dual p38α/MAPKAPK-2 and PK-N3 signaling pathway

enthalten in: Chemical research in toxicology | 2015

von Chen, H. | Wang, T. | Lee, Y. | +12

85

Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations

enthalten in: European journal of medicinal chemistry | 2015

von Chen, C. | Hsu, J. | Lin, W. | +15

86

1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells

enthalten in: European journal of medicinal chemistry | 2015

von Liu, Y. | Lee, H. | Chen, C. | +6

87

Novel Nrf2/ARE activator, trans-Coniferylaldehyde, induces a HO-1-mediated defense mechanism through a dual p38α/MAPKAPK-2 and PK-N3 signaling pathway

enthalten in: Chemical research in toxicology | 2015

von Chen, H. | Wang, T. | Lee, Y. | +12

88

2-Aroylquinoline-5,8-diones as potent anticancer agents displaying tubulin and heat shock protein 90 (HSP90) inhibition

enthalten in: Organic & biomolecular chemistry | 2015

von Nepali, K. | Kumar, S. | Huang, H. | +8

89

1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells

enthalten in: European journal of medicinal chemistry | 2015

von Liu, Y. | Lee, H. | Chen, C. | +6

90

Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations

enthalten in: European journal of medicinal chemistry | 2015

von Chen, C. | Hsu, J. | Lin, W. | +15