| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
L-Proline catalyzed one-step synthesis of 4,5-diaryl-2H-1,2,3-triazoles from heteroaryl cyanostilbenes via [3+2] cycloaddition of azide.
|
Tetrahedron Lett
|
2014
|
1.07
|
|
2
|
(E)-13-(4-Amino-phen-yl)parthenolide.
|
Acta Crystallogr Sect E Struct Rep Online
|
2013
|
0.96
|
|
3
|
Synthesis and anti-proliferative activity of aromatic substituted 5-((1-benzyl-1H-indol-3-yl)methylene)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione analogs against human tumor cell lines.
|
Bioorg Med Chem Lett
|
2013
|
0.92
|
|
4
|
Anti-cancer activity of carbamate derivatives of melampomagnolide B.
|
Bioorg Med Chem Lett
|
2014
|
0.88
|
|
5
|
Crystal structure of (E)-13-{4-[(Z)-2-cyano-2-(3,4,5-tri-meth-oxy-phen-yl)ethen-yl]phen-yl}parthenolide methanol hemisolvate.
|
Acta Crystallogr Sect E Struct Rep Online
|
2014
|
0.81
|
|
6
|
Identification of a melampomagnolide B analog as a potential lead molecule for treatment of acute myelogenous leukemia.
|
Bioorg Med Chem
|
2016
|
0.80
|
|
7
|
Heck products of parthenolide and melampomagnolide-B as anticancer modulators that modify cell cycle progression.
|
Eur J Med Chem
|
2014
|
0.79
|
|
8
|
1,4-Diphenalkylpiperidines: A new scaffold for the design of potent inhibitors of the vesicular monoamine transporter-2.
|
Bioorg Med Chem Lett
|
2016
|
0.78
|
|
9
|
Heterocyclic aminoparthenolide derivatives modulate G(2)-M cell cycle progression during Xenopus oocyte maturation.
|
Bioorg Med Chem Lett
|
2014
|
0.78
|
|
10
|
Synthesis and evaluation of a series of resveratrol analogues as potent anti-cancer agents that target tubulin.
|
Medchemcomm
|
2015
|
0.78
|
|
11
|
Synthesis and in vitro evaluation of water-soluble 1,4-diphenethylpiperazine analogs as novel inhibitors of the vesicular monoamine transporter-2.
|
Bioorg Med Chem Lett
|
2016
|
0.75
|
|
12
|
13-(Imidazol-1-yl)-11,13-di-hydro-melampomagnolide B monohydrate.
|
Acta Crystallogr Sect E Struct Rep Online
|
2013
|
0.75
|
|
13
|
(E)-13-(2-Bromo-phen-yl)micheliolide.
|
Acta Crystallogr Sect E Struct Rep Online
|
2014
|
0.75
|
|
14
|
Lobelane analogues containing 4-hydroxy and 4-(2-fluoroethoxy) aromatic substituents: Potent and selective inhibitors of [(3)H]dopamine uptake at the vesicular monoamine transporter-2.
|
Bioorg Med Chem Lett
|
2016
|
0.75
|
|
15
|
Monosuccinate ester of melampomagnolide B.
|
Acta Crystallogr Sect E Struct Rep Online
|
2014
|
0.75
|
|
16
|
Succinamide derivatives of melampomagnolide B and their anti-cancer activities.
|
Bioorg Med Chem
|
2017
|
0.75
|
|
17
|
Fluoroethoxy-1,4-diphenethylpiperidine and piperazine derivatives: Potent and selective inhibitors of [3H]dopamine uptake at the vesicular monoamine transporter-2.
|
Bioorg Med Chem Lett
|
2017
|
0.75
|
|
18
|
Indole carboxylic acid esters of melampomagnolide B are potent anticancer agents against both hematological and solid tumor cells.
|
Eur J Med Chem
|
2017
|
0.75
|