Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Elaboration of 2-(trifluoromethyl)indoles via a cascade coupling/condensation/deacylation process.
|
Org Lett
|
2008
|
0.98
|
2
|
Follistatin-like protein 1 is elevated in systemic autoimmune diseases and correlated with disease activity in patients with rheumatoid arthritis.
|
Arthritis Res Ther
|
2011
|
0.96
|
3
|
A class of novel carboline intercalators: Their synthesis, in vitro anti-proliferation, in vivo anti-tumor action, and 3D QSAR analysis.
|
Bioorg Med Chem
|
2010
|
0.88
|
4
|
Nanosized aspirin-Arg-Gly-Asp-Val: delivery of aspirin to thrombus by the target carrier Arg-Gly-Asp-Val tetrapeptide.
|
ACS Nano
|
2013
|
0.87
|
5
|
Facile benzo-ring construction via palladium-catalyzed functionalization of unactivated sp3 C-H bonds under mild reaction conditions.
|
Org Lett
|
2010
|
0.83
|
6
|
Assembly of substituted 1H-benzimidazoles and 1,3-dihydrobenzimidazol-2-ones via CuI/L-proline catalyzed coupling of aqueous ammonia with 2-iodoacetanilides and 2-iodophenylcarbamates.
|
J Org Chem
|
2009
|
0.82
|
7
|
{2-[1-(3-Methoxycarbonylmethyl-1H-indol-2-yl)-1-methyl-ethyl]-1H-indol-3-yl}-acetic acid methyl ester (MIAM): its anti-cancer efficacy and intercalation mechanism identified via multi-model systems.
|
Mol Biosyst
|
2010
|
0.82
|
8
|
Assembly of beta-cyclodextrin with 3S-tetrahydro-beta-carboline-3-carboxylic acid and self-assembly of 6-(3'S-carboline-3'-carboxylaminoethylamino)-6-deoxy-beta-cyclodextrin: approaches to enhance anti-oxidation stability and anti-thrombotic potency.
|
J Phys Chem B
|
2008
|
0.81
|
9
|
Pyranoflavones: a group of small-molecule probes for exploring the active site cavities of cytochrome P450 enzymes 1A1, 1A2, and 1B1.
|
J Med Chem
|
2013
|
0.80
|
10
|
The application of tetrahydroisoquinoline-3-carbonyl-TARGD(F)F as an anti-thrombotic agent having dual mechanisms of action.
|
Mol Biosyst
|
2012
|
0.79
|
11
|
[Resurfacing arthroplasty for treatment of avascular necrosis of femoral head in young and middle-aged patients].
|
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi
|
2005
|
0.78
|
12
|
A class of novel N-(1-methyl-β-carboline-3-carbonyl)-N'-(aminoacid-acyl)-hydrazines: aromatization leaded design, synthesis, in vitro anti-platelet aggregation/in vivo anti-thrombotic evaluation and 3D QSAR analysis.
|
Eur J Med Chem
|
2011
|
0.78
|
13
|
Poly-α,β-DL-aspartyl-L-cysteine: a novel nanomaterial having a porous structure, special complexation capability for Pb(II), and selectivity of removing Pb(II).
|
Chem Res Toxicol
|
2012
|
0.78
|
14
|
One single HPLC-PDA/(-)ESI-MS/MS analysis to simultaneously determine 30 components of the aqueous extract of Rabdosia rubescens.
|
J Chromatogr B Analyt Technol Biomed Life Sci
|
2011
|
0.78
|
15
|
MDM4 overexpression contributes to synoviocyte proliferation in patients with rheumatoid arthritis.
|
Biochem Biophys Res Commun
|
2010
|
0.78
|
16
|
Lead detoxification activities and ADMET hepatotoxicities of a class of novel 5-(1-carbonyl-L-amino-acid)-2,2-dimethyl-[1,3]dithiolane-4-carboxylic acids.
|
Bioorg Med Chem Lett
|
2011
|
0.77
|
17
|
A class of novel N-isoquinoline-3-carbonyl-L-amino acid benzylesters: synthesis, anti-tumor evaluation and 3D QSAR analysis.
|
Eur J Med Chem
|
2011
|
0.77
|
18
|
Preparation and Characterization of RGDS/Nanodiamond as a Vector for VEGF-siRNA Delivery.
|
J Biomed Nanotechnol
|
2015
|
0.77
|
19
|
Alsterpaullone, a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells through Apoptosis-Inducing Effect.
|
J Anal Methods Chem
|
2013
|
0.77
|
20
|
A class of oral N-[(1S,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carbonyl]- N'-(amino-acid-acyl)hydrazine: discovery, synthesis, in vitro anti-platelet aggregation/in vivo anti-thrombotic evaluation and 3D QSAR analysis.
|
Eur J Med Chem
|
2011
|
0.77
|
21
|
Pyrolo[1,2:4,5]-1,4-dioxopyrazino[1,2:1,6]pyrido[3,4-b]indoles: a group of urokinase inhibitors, their synthesis, and stereochemistry-dependent activity.
|
ChemMedChem
|
2011
|
0.77
|
22
|
Oximated ruthenium tris-bipyridyl complex: synthesis and luminescent response specifically for ClO(-) in water containing multiple ions.
|
Dalton Trans
|
2015
|
0.76
|
23
|
(3S)-N-(L-Aminoacyl)-1,2,3,4-tetrahydroisoquinolines, a class of novel antithrombotic agents: synthesis, bioassay, 3D QSAR, and ADME analysis.
|
Bioorg Med Chem
|
2008
|
0.76
|
24
|
Folded Conformation, Cyclic Pentamer, Nano-Structure and PAD4 Binding Mode of YW3-56.
|
J Phys Chem C Nanomater Interfaces
|
2013
|
0.76
|
25
|
Exploring the Relationship between the Inhibition Selectivity and the Apoptosis of Roscovitine-Treated Cancer Cells.
|
J Anal Methods Chem
|
2013
|
0.76
|
26
|
Lead detoxification activity and ADMET hepatotoxicity of N-(alpha-L-arabino-furanos-1-yl)-L-cysteine.
|
Chem Res Toxicol
|
2010
|
0.76
|
27
|
Synthesis and in vivo lead detoxification evaluation of Poly-α,β-dl-aspartyl-l-methionine.
|
Chem Res Toxicol
|
2012
|
0.76
|
28
|
Design and Synthesis of Biotinylated Bivalent Carboline Derivatives as Potent Anti-tumor Agents.
|
J Org Chem
|
2020
|
0.75
|
29
|
[Discussion on the electromagnetic compatibility testing and evaluation of radio frequency ablation catheter].
|
Zhongguo Yi Liao Qi Xie Za Zhi
|
2014
|
0.75
|
30
|
Lead detoxification activities of a class of novel DMSA--amino acid conjugates.
|
Chem Res Toxicol
|
2011
|
0.75
|
31
|
A class of Trp-Trp-AA-OBzl: Synthesis, in vitro anti-proliferation/in vivo anti-tumor evaluation, intercalation-mechanism investigation and 3D QSAR analysis.
|
Eur J Med Chem
|
2011
|
0.75
|
32
|
Diastereoselective aldol reaction of N,N-dibenzyl-alpha-amino aldehydes with ketones catalyzed by proline.
|
Org Lett
|
2004
|
0.75
|
33
|
ImmunoFET feasibility in physiological salt environments.
|
Philos Trans A Math Phys Eng Sci
|
2012
|
0.75
|
34
|
pH-Dependent nanostructure based on isoquinoline-cyclodextrin conjugate for thrombosis therapy.
|
Nanomedicine
|
2012
|
0.75
|
35
|
2-Substituted (S)-2-(3,3-dimethyl-1-oxo-10,10a-dihydroimidazo[1,5-b]isoquinolin-2(1H,3H,5H)-yl)acetic acids: Conformational prediction, synthesis, anti-thrombotic and vasodilative evaluation.
|
Bioorg Med Chem
|
2010
|
0.75
|
36
|
From Cerius² based stereoview to mouse and enzyme: the model systems for discovery of novel urokinase inhibitors.
|
Mol Biosyst
|
2011
|
0.75
|