Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Antiviral activities and cellular toxicities of modified 2',3'-dideoxy-2',3'-didehydrocytidine analogues.
|
Antimicrob Agents Chemother
|
2002
|
1.79
|
2
|
5- And 6-exocyclic products, cis-2,3,5-trisubstituted tetrahydrofurans, and cis-2,3,6-trisubstituted tetrahydropyrans via Prins-type cyclization.
|
J Org Chem
|
2008
|
1.06
|
3
|
L-nucleosides: antiviral activity and molecular mechanism.
|
Curr Top Med Chem
|
2002
|
0.99
|
4
|
Novel GSK-3beta inhibitors from sequential virtual screening.
|
Bioorg Med Chem
|
2007
|
0.92
|
5
|
5-Exocyclic products, 2,3,5-trisubstituted tetrahydrofurans via Prins-type cyclization.
|
Org Lett
|
2006
|
0.92
|
6
|
Novel quinazolinone derivatives as 5-HT7 receptor ligands.
|
Bioorg Med Chem
|
2007
|
0.86
|
7
|
KST5468, a new T-type calcium channel antagonist, has an antinociceptive effect on inflammatory and neuropathic pain models.
|
Pharmacol Biochem Behav
|
2010
|
0.86
|
8
|
IKKbeta inhibitors identification part II: ligand and structure-based virtual screening.
|
Bioorg Med Chem
|
2010
|
0.85
|
9
|
Synthesis, structure-activity relationships, and mechanism of drug resistance of D- and L-beta-3'-fluoro-2',3'-unsaturated-4'-thionucleosides as anti-HIV agents.
|
J Med Chem
|
2004
|
0.83
|
10
|
In vitro solubility, stability and permeability of novel quercetin-amino acid conjugates.
|
Bioorg Med Chem
|
2008
|
0.80
|
11
|
Stereoselective synthesis and antiviral activity of D-2',3'-didehydro-2',3'-dideoxy-2'-fluoro-4'-thionucleosides.
|
J Med Chem
|
2002
|
0.80
|
12
|
IKKβ inhibitor identification: a multi-filter driven novel scaffold.
|
BMC Bioinformatics
|
2010
|
0.80
|
13
|
IKKbeta inhibitors identification part I: homology model assisted structure based virtual screening.
|
Bioorg Med Chem
|
2009
|
0.80
|
14
|
New serotonin 5-HT(6) ligands from common feature pharmacophore hypotheses.
|
J Chem Inf Model
|
2007
|
0.79
|
15
|
4-Aminoethylpiperazinyl aryl ketones with 5-HT₁A/5-HT₇ selectivity.
|
Bioorg Med Chem
|
2011
|
0.79
|
16
|
Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors.
|
Bioorg Med Chem Lett
|
2011
|
0.79
|
17
|
Identification of novel serotonin 2C receptor ligands by sequential virtual screening.
|
Bioorg Med Chem
|
2009
|
0.79
|
18
|
Enhanced stability and intracellular accumulation of quercetin by protection of the chemically or metabolically susceptible hydroxyl groups with a pivaloxymethyl (POM) promoiety.
|
J Med Chem
|
2010
|
0.79
|
19
|
Water-soluble and cleavable quercetin-amino acid conjugates as safe modulators for P-glycoprotein-based multidrug resistance.
|
J Med Chem
|
2014
|
0.78
|
20
|
3D QSAR pharmacophore model based on diverse IKKβ inhibitors.
|
J Mol Model
|
2010
|
0.78
|
21
|
Synthesis of beta-enantiomers of N4-hydroxy-3'-deoxypyrimidine nucleosides and their evaluation against bovine viral diarrhoea virus and hepatitis C virus in cell culture.
|
Antivir Chem Chemother
|
2004
|
0.78
|
22
|
Classification of dopamine, serotonin, and dual antagonists by decision trees.
|
Bioorg Med Chem
|
2006
|
0.78
|
23
|
Quercetin-POC conjugates: Differential stability and bioactivity profiles between breast cancer (MCF-7) and colorectal carcinoma (HCT116) cell lines.
|
Bioorg Med Chem
|
2013
|
0.78
|
24
|
Dicyanovinyl-substituted J147 analogue inhibits oligomerization and fibrillation of β-amyloid peptides and protects neuronal cells from β-amyloid-induced cytotoxicity.
|
Org Biomol Chem
|
2015
|
0.77
|
25
|
Oxazolopyridines and thiazolopyridines as monoamine oxidase B inhibitors for the treatment of Parkinson's disease.
|
Bioorg Med Chem
|
2013
|
0.77
|
26
|
Quinazolindione derivatives as potent 5-HT3A receptor antagonists.
|
Bioorg Med Chem
|
2009
|
0.77
|
27
|
Novel T-type calcium channel blockers: dioxoquinazoline carboxamide derivatives.
|
Bioorg Med Chem
|
2006
|
0.77
|
28
|
Synthesis and biological evaluation of oxazole derivatives as T-type calcium channel blockers.
|
Bioorg Med Chem Lett
|
2010
|
0.77
|
29
|
Synthesis and potent anti-HIV activity of L-2',3'-didehydro-2',3'-dideoxy-2'-fluoro-4'-thiocytidine.
|
Org Lett
|
2002
|
0.77
|
30
|
2,6-Bis-arylmethyloxy-5-hydroxychromones with antiviral activity against both hepatitis C virus (HCV) and SARS-associated coronavirus (SCV).
|
Eur J Med Chem
|
2011
|
0.77
|
31
|
3D pharmacophore based virtual screening of T-type calcium channel blockers.
|
Bioorg Med Chem
|
2006
|
0.77
|
32
|
Effects of fluorine substitution of cytosine analogues on the binding affinity to HIV-1 reverse transcriptase.
|
Bioorg Med Chem Lett
|
2004
|
0.76
|
33
|
Design, synthesis, and biological evaluation of 1,3-dioxoisoindoline-5-carboxamide derivatives as T-type calcium channel blockers.
|
Bioorg Med Chem Lett
|
2006
|
0.75
|
34
|
5-HT₃ antagonists under development.
|
Expert Opin Investig Drugs
|
2010
|
0.75
|
35
|
Comparative QSAR studies on peptide deformylase inhibitors.
|
J Mol Model
|
2007
|
0.75
|
36
|
Facile diverted synthesis of pyrrolidinyl triazoles using organotrifluoroborate: discovery of potential mPTP blockers.
|
Org Biomol Chem
|
2014
|
0.75
|
37
|
Selective inhibition of the hypoxia-inducible factor prolyl hydroxylase PHD3 by Zn(II).
|
Chem Commun (Camb)
|
2015
|
0.75
|
38
|
Synthesis and the 5-HT6 receptor antagonistic effect of 3-arylsulfonylamino-5,6-dihydro-6-substituted pyrazolo[3,4]pyridinones for neuropathic pain treatment.
|
Bioorg Med Chem Lett
|
2013
|
0.75
|
39
|
Separation of quercetin's biological activity from its oxidative property through bioisosteric replacement of the catecholic hydroxyl groups with fluorine atoms.
|
J Agric Food Chem
|
2012
|
0.75
|
40
|
Novel 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-one derivatives as potential anti-cancer agents.
|
Bioorg Med Chem Lett
|
2010
|
0.75
|
41
|
Synthesis and biological evaluation of aryloxazole derivatives as antimitotic and vascular-disrupting agents for cancer therapy.
|
J Med Chem
|
2013
|
0.75
|
42
|
Aryl biphenyl-3-ylmethylpiperazines as 5-HT7 receptor antagonists.
|
ChemMedChem
|
2013
|
0.75
|
43
|
Antiviral activity of nucleoside analogues against SARS-coronavirus (SARS-coV).
|
Antivir Chem Chemother
|
2006
|
0.75
|
44
|
Discovery of aryl-biphenyl-2-ylmethylpiperazines as novel scaffolds for 5-HT(7) ligands and role of the aromatic substituents in binding to the target receptor.
|
Bioorg Med Chem
|
2013
|
0.75
|
45
|
2'-Fluoro-4'-thio-2',3'-unsaturated nucleosides: anti-HIV activity, resistance profile, and molecular modeling studies.
|
Nucleosides Nucleotides Nucleic Acids
|
2003
|
0.75
|
46
|
Synthesis and antibacterial activities of new piperidine substituted (5R)-[1,2,3]triazolylmethyl and (5R)-[(4-F-[1,2,3]triazolyl)methyl] oxazolidinones.
|
Bioorg Med Chem Lett
|
2013
|
0.75
|
47
|
Synthesis and in vitro evaluation of the antitubercular and antibacterial activity of novel oxazolidinones bearing octahydrocyclopenta[c]pyrrol-2-yl moieties.
|
Chem Pharm Bull (Tokyo)
|
2014
|
0.75
|
48
|
Intermolecular double Prins-type cyclization: a facile and efficient synthesis of 1,6-dioxecanes.
|
Angew Chem Int Ed Engl
|
2009
|
0.75
|