Science Explorer Back to mapMap
Institution · Arqule (United States)

Most cited papers from Arqule (United States)

What are the most cited papers from Arqule (United States)?

The most cited paper from Arqule (United States) is "Towards a proteome-scale map of the human protein–protein interaction network" (Jean‐François Rual et al., 2005), with 3,034 citations. Next come "Tivantinib for second-line treatment of advanced hepatocellular carcinoma: a randomised, placebo-controlled phase 2 study" (558) and "Derazantinib (ARQ 087) in advanced or inoperable FGFR2 gene fusion-positive intrahepatic cholangiocarcinoma" (385).

Showing 50 of 60 papers. Every paper with more than 65 citations is listed.

Most cited papers, sortable by citations and release date
#Paper
1 Towards a proteome-scale map of the human protein–protein interaction network Jean‐François Rual et al. · Nature 27 Sep 2005 3,034
2 Tivantinib for second-line treatment of advanced hepatocellular carcinoma: a randomised, placebo-controlled phase 2 study Armando Santoro et al. · The Lancet Oncology 19 Nov 2012 558
3 Derazantinib (ARQ 087) in advanced or inoperable FGFR2 gene fusion-positive intrahepatic cholangiocarcinoma Vincenzo Mazzaferro, Bassel F. El‐Rayes, Michele Droz Dit Busset et al. · British Journal of Cancer Open access 7 Nov 2018 385
4 Tivantinib for second-line treatment of MET-high, advanced hepatocellular carcinoma (METIV-HCC): a final analysis of a phase 3, randomised, placebo-controlled study Lorenza Rimassa et al. · The Lancet Oncology 3 Apr 2018 356
5 The effect of tobacco cessation on weight gain, obesity, and diabetes risk Terry M. Bush, Jennifer C. Lovejoy, Mona Deprey et al. · Obesity Open access 29 Aug 2016 231
6 Modular Synthesis of Heparin Oligosaccharides Hernán A. Orgueira, Alessandra Bartolozzi, Peter Schell et al. · Chemistry - A European Journal 30 Dec 2002 216
7 Phase I Trial of a Selective c-MET Inhibitor ARQ 197 Incorporating Proof of Mechanism Pharmacodynamic Studies Timothy Anthony Yap, David Olmos, Andre Tesainer Brunetto et al. · Journal of Clinical Oncology Open access 8 Mar 2011 196
8 Kinetic analysis of a high-affinity antibody/antigen interaction performed by multiple Biacore users Phinikoula S. Katsamba et al. · Analytical Biochemistry 24 Feb 2006 186
9 Toward an Optimal Procedure for Variable Selection and QSAR Model Building Abdelaziz Yasri, David S. Hartsough · Journal of Chemical Information and Computer Sciences Aug 2001 178
10 Automated parallel synthesis of chalcone-based screening libraries David G. Powers, David S. Casebier, Demosthenes Fokas et al. · Tetrahedron Apr 1998 177
11 c-Met is a prognostic marker and potential therapeutic target in clear cell renal cell carcinoma Geoffrey Thomas Gibney, Saadia A. Aziz, Robert L. Camp et al. · Annals of Oncology Open access 30 Sep 2012 177
12 The BTK Inhibitor ARQ 531 Targets Ibrutinib-Resistant CLL and Richter Transformation Sean D. Reiff et al. · Cancer Discovery Open access 9 Aug 2018 171
13 Multi-functional nanocarriers for targeted delivery of drugs and genes Lara Scheherazade Jabr-Milane, Lilian van Vlerken, Harikrishna Devalapally et al. · Journal of Controlled Release 30 Apr 2008 170
14 Binding of Polyubiquitin Chains to Ubiquitin-associated (UBA) Domains of HHR23A Shahri Raasi, Irina Orlov, Karen G. Fleming et al. · Journal of Molecular Biology Aug 2004 160
15 Tivantinib (ARQ 197), a selective inhibitor of MET, in patients with microphthalmia transcription factor–associated tumors Andrew J. Wagner, John M. Goldberg, Steven G. DuBois et al. · Cancer 17 May 2012 156
16 Regioselective synthesis of [1,2,3]-triazoles catalyzed by Cu(I) generated in situ from Cu(0) nanosize activated powder and amine hydrochloride salts Hernán A. Orgueira, Demosthenes Fokas, Yuko Isome et al. · Tetrahedron Letters 11 Mar 2005 150
17 Discovery of a Novel Mode of Protein Kinase Inhibition Characterized by the Mechanism of Inhibition of Human Mesenchymal-epithelial Transition Factor (c-Met) Protein Autophosphorylation by ARQ 197 Sudharshan Eathiraj, Rocio Palma, Erika Volckova et al. · Journal of Biological Chemistry Open access 25 Mar 2011 141
18 Pteridine reductase mechanism correlates pterin metabolism with drug resistance in trypanosomatid parasites. David G. Gourley, Alexander W. Schüttelkopf, Gordon A. Leonard et al. · Nature Structural Biology Jun 2001 139
19 Microwave-assisted one-pot synthesis of 2,3-disubstituted 3H-quinazolin-4-ones Jifeng Liu, Jaekyoo Lee, Audra M. Dalton et al. · Tetrahedron Letters 25 Jan 2005 137
20 Cytoskeletal stiffness, friction, and fluidity of cancer cell lines with different metastatic potential Mark F. Coughlin, Diane Renee Bielenberg, Guillaume Lenormand et al. · Clinical & Experimental Metastasis Open access 7 Sep 2012 128
21 Rationale and Design of MARQUEE: A Phase III, Randomized, Double-Blind Study of Tivantinib Plus Erlotinib Versus Placebo Plus Erlotinib in Previously Treated Patients With Locally Advanced or Metastatic, Nonsquamous, Non–Small-Cell Lung Cancer Giorgio V. Scagliotti, Silvia Novello, Joan H. Schiller et al. · Clinical Lung Cancer Open access 21 Mar 2012 126
22 Targeting AKT1-E17K and the PI3K/AKT Pathway with an Allosteric AKT Inhibitor, ARQ 092 Yi Yu, Ronald E. Savage, Sudharshan Eathiraj et al. · PLoS ONE Open access 15 Oct 2015 122
23 Discovery of 3-(3-(4-(1-Aminocyclobutyl)phenyl)-5-phenyl-3 H -imidazo[4,5- b ]pyridin-2-yl)pyridin-2-amine (ARQ 092): An Orally Bioavailable, Selective, and Potent Allosteric AKT Inhibitor Jean‐Marc Lapierre, Sudharshan Eathiraj, David Vensel et al. · Journal of Medicinal Chemistry Open access 15 Jun 2016 117
24 Specific Structural Motifs Determine TRAP220 Interactions with Nuclear Hormone Receptors Yunsheng Ren, Evan Behre, Zhaojun Ren et al. · Molecular and Cellular Biology Open access Aug 2000 117
25 Structure-based design of parasitic protease inhibitors Rongshi Li, Xiaowu Chen, Baoqing Gong et al. · Bioorganic & Medicinal Chemistry Open access Sep 1996 115
26 Purification of Proteasomes, Proteasome Subcomplexes, and Proteasome-Associated Proteins From Budding Yeast David Leggett, Michael H. Glickman, Daniel Finley · Humana Press eBooks Book chapter 25 May 2005 114
27 Use of Support Vector Machine in Pattern Classification: Application to QSAR Studies Ryszard Czermiński, Abdelaziz Yasri, David S. Hartsough · Quantitative Structure-Activity Relationships Oct 2001 111
28 Microwave-assisted one step high-throughput synthesis of benzimidazoles Shou‐Yuan Lin, Yuko Isome, E. Theal Stewart et al. · Tetrahedron Letters 10 Mar 2006 109
29 Discovery and Optimization of a Series of 3-(3-Phenyl-3 H -imidazo[4,5- b ]pyridin-2-yl)pyridin-2-amines: Orally Bioavailable, Selective, and Potent ATP-Independent Akt Inhibitors Mark A. Ashwell et al. · Journal of Medicinal Chemistry Open access 25 Apr 2012 109
30 Phase 1 study of ARQ 761, a β-lapachone analogue that promotes NQO1-mediated programmed cancer cell necrosis David E. Gerber, Muhammad Shaalan Beg, Farjana Jahan Fattah et al. · British Journal of Cancer Open access Oct 2018 104
31 Rescue of paclitaxel sensitivity by repression of Prohibitin1 in drug-resistant cancer cells Nish Patel, Sabarni K. Chatterjee, Vladimir D. Vrbanac et al. · Proceedings of the National Academy of Sciences Open access 25 Jan 2010 104
32 Novel One-Pot Total Syntheses of Deoxyvasicinone, Mackinazolinone, Isaindigotone, and Their Derivatives Promoted by Microwave Irradiation Jifeng Liu, Ye Ping, Kevin Sprague et al. · Organic Letters 22 Jun 2005 103
33 Detecting hidden sequence propensity for amyloid fibril formation Sukjoon Yoon, William Jeffrey Welsh · Protein Science Open access 23 Jul 2004 103
34 A Phase 1 study of ARQ 087, an oral pan-FGFR inhibitor in patients with advanced solid tumours Kyriakos P. Papadopoulos, Bassell F. El-Rayes, Anthony W. Tolcher et al. · British Journal of Cancer Open access 3 Oct 2017 97
35 Pharmacodynamic Study of Miransertib in Individuals with Proteus Syndrome Kim M. Keppler‐Noreuil, Julie C. Sapp, Marjorie J. Lindhurst et al. · The American Journal of Human Genetics Open access 22 Feb 2019 95
36 Solution phase synthesis of a spiro[pyrrolidine-2,3′-oxindole] library via a three component 1,3-dipolar cycloaddition reaction Demosthenes Fokas, William J. Ryan, David S. Casebier et al. · Tetrahedron Letters Apr 1998 93
37 Development of α-keto-based inhibitors of cruzain, a cysteine protease implicated in Chagas disease Youngchool Choe, Linda S. Brinen, Mark S. Price et al. · Bioorganic & Medicinal Chemistry 10 Feb 2005 91
38 Preclinical Activity of ARQ 087, a Novel Inhibitor Targeting FGFR Dysregulation Terence G. Hall, Yi Yu, Sudharshan Eathiraj et al. · PLoS ONE Open access 14 Sep 2016 88
39 Three-Component One-Pot Total Syntheses of Glyantrypine, Fumiquinazoline F, and Fiscalin B Promoted by Microwave Irradiation Jifeng Liu, Ye Ping, Bailin Zhang et al. · The Journal of Organic Chemistry Jul 2005 88
40 DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease risk Helmut Grasberger, Andrew T. Magis, Elisa Sheng et al. · Journal of Clinical Investigation Open access 2 Mar 2021 84
41 In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) Carlotta Ranieri et al. · Neurogenetics Open access 16 Mar 2018 83
42 Macamides and their synthetic analogs: Evaluation of in vitro FAAH inhibition Hui Ming Wu, Charles J. Kelley, Alejandro J Pino‐Figueroa et al. · Bioorganic & Medicinal Chemistry Open access 27 Jun 2013 83
43 A phase I dose escalation study of oral c-MET inhibitor tivantinib (ARQ 197) in combination with gemcitabine in patients with solid tumors Shubham Pant, Mansoor Noorali Saleh, Johanna C. Bendell et al. · Annals of Oncology Open access 16 Apr 2014 83
44 Combinatorial chemistry in drug discovery Joseph C. Hogan · Nature Biotechnology Apr 1997 83
45 Inhibition of the BTK-IDO-mTOR axis promotes differentiation of monocyte-lineage dendritic cells and enhances anti-tumor T cell immunity Madhav D. Sharma, Rafał Pacholczyk, Huidong Shi et al. · Immunity Open access Oct 2021 81
46 Synthesis of 21,21-Difluoro-3β-hydroxy-20-methylpregna-5,20-diene and 5,16,20-Triene as potential inhibitors of steroid C17(20) lyase Philip M. Weintraub, Amy K. Holland, Cynthia A. Gates et al. · Bioorganic & Medicinal Chemistry Feb 2003 79
47 A Phase-1b study of tivantinib (ARQ 197) in adult patients with hepatocellular carcinoma and cirrhosis Armando Santoro, Matteo Simonelli, C Rodriguez-Lope et al. · British Journal of Cancer Open access 2013 78
48 Phase 1 dose‐escalation trial evaluating the combination of the selective MET (mesenchymal‐epithelial transition factor) inhibitor tivantinib (ARQ 197) plus erlotinib Jonathan Wade Goldman, Isett Laux, Feng Chai et al. · Cancer Open access 17 May 2012 77
49 Pharmacological induction of Hsp70 protects apoptosis-prone cells from doxorubicin: comparison with caspase-inhibitor- and cycle-arrest-mediated cytoprotection Zoya N. Demidenko, Claire Vivo, H. Dorota Halicka et al. · Cell Death and Differentiation 25 Nov 2005 77
50 The accelerated development of an optimized synthesis of 1,2,4-oxadiazoles: application of microwave irradiation and statistical design of experiments Marc D Evans, Jessica Ring, Adam William Schoen et al. · Tetrahedron Letters Dec 2003 77

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.