skip to main content
Language:
Show Results with:
Refined by: author: Wang, Ying remove subject: Antineoplastic Agents remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Synthesis and c-Met kinase inhibition of 3,5-disubstituted and 3,5,7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7- (trifluoromethyl)quinoline as a novel anticancer agent.
Synthesis and c-Met kinase inhibition of 3,5-disubstituted and 3,5,7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7- (trifluoromethyl)quinoline as a novel anticancer agent.
Material Type:
Article 		Add to My workspace

Synthesis and c-Met kinase inhibition of 3,5-disubstituted and 3,5,7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7- (trifluoromethyl)quinoline as a novel anticancer agent.

Journal of medicinal chemistry, April 14, 2011, Vol.54(7), pp.2127-2142 [Peer Reviewed Journal]

No full-text

View all versions
2
Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluation.
Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluation.
Material Type:
Article 		Add to My workspace

Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluation.

ChemMedChem, June 2012, Vol.7(6), pp.1057-1070 [Peer Reviewed Journal]

No full-text

View all versions
3
SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.
SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.
Material Type:
Article 		Add to My workspace

SAR of amino pyrrolidines as potent and novel protein-protein interaction inhibitors of the PRC2 complex through EED binding.

Bioorganic & medicinal chemistry letters, April 1, 2017, Vol.27(7), pp.1576-1583 [Peer Reviewed Journal]

No full-text

View all versions
4
Synthesis and biological evaluation of 2-amino-5-aryl-3-benzylthiopyridine scaffold based potent c-Met inhibitors.
Synthesis and biological evaluation of 2-amino-5-aryl-3-benzylthiopyridine scaffold based potent c-Met inhibitors.
Material Type:
Article 		Add to My workspace

Synthesis and biological evaluation of 2-amino-5-aryl-3-benzylthiopyridine scaffold based potent c-Met inhibitors.

Bioorganic & medicinal chemistry, November 1, 2013, Vol.21(21), pp.6804-6820 [Peer Reviewed Journal]

No full-text

View all versions
5
The application of click chemistry in the synthesis of agents with anticancer activity
The application of click chemistry in the synthesis of agents with anticancer activity
Material Type:
Article 		Add to My workspace

The application of click chemistry in the synthesis of agents with anticancer activity

Drug Design, Development and Therapy, 2015, Vol.9, pp.1585-1599 [Peer Reviewed Journal]

Full text available

View all versions
6
The anti-hepatocellular carcinoma cell activity by a novel mTOR kinase inhibitor CZ415.
The anti-hepatocellular carcinoma cell activity by a novel mTOR kinase inhibitor CZ415.
Material Type:
Article 		Add to My workspace

The anti-hepatocellular carcinoma cell activity by a novel mTOR kinase inhibitor CZ415.

Biochemical and biophysical research communications, June 3, 2017, Vol.487(3), pp.494-499 [Peer Reviewed Journal]

No full-text

View all versions
7
Design, synthesis and evaluation of 6-aryl-indenoisoquinolone derivatives dual targeting ERα and VEGFR-2 as anti-breast cancer agents.
Design, synthesis and evaluation of 6-aryl-indenoisoquinolone derivatives dual targeting ERα and VEGFR-2 as anti-breast cancer agents.
Material Type:
Article 		Add to My workspace

Design, synthesis and evaluation of 6-aryl-indenoisoquinolone derivatives dual targeting ERα and VEGFR-2 as anti-breast cancer agents.

European journal of medicinal chemistry, August 8, 2016, Vol.118, pp.328-339 [Peer Reviewed Journal]

No full-text

View all versions
8
Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines.
Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines.
Material Type:
Article 		Add to My workspace

Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines.

Bioorganic & medicinal chemistry letters, March 1, 2006, Vol.16(5), pp.1191-1196 [Peer Reviewed Journal]

No full-text

View all versions

Refine Search Results

Creation date 

From To
Refine
  1. Before2011  (1)
  2. 2011To2011  (1)
  3. 2012To2012  (1)
  4. 2013To2015  (2)
  5. After 2015  (3)
  6. Refine further open sub menu

Try a new search

Ignore my search and look for everything

by this Author/Contributor:

  1. Wang, Ying
  2. Wang, Y.
  3. Chen, Yi
  4. Ai, Jing
  5. Geng, Meiyu

on this subject:

  1. Humans
  2. Chemistry
  3. Cell Line, Tumor
  4. Cell Proliferation
  5. Protein Kinase Inhibitors

All text is © British Library Board and is available under a Creative Commons Attribution Licence, except where otherwise stated.

P1

Searching Remote Databases, Please Wait