John Drewe

5.5k total citations
62 papers, 4.6k citations indexed

About

John Drewe is a scholar working on Molecular Biology, Organic Chemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, John Drewe has authored 62 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 33 papers in Organic Chemistry and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in John Drewe's work include Synthesis and biological activity (20 papers), Synthesis and Characterization of Heterocyclic Compounds (14 papers) and Neuroscience and Neuropharmacology Research (13 papers). John Drewe is often cited by papers focused on Synthesis and biological activity (20 papers), Synthesis and Characterization of Heterocyclic Compounds (14 papers) and Neuroscience and Neuropharmacology Research (13 papers). John Drewe collaborates with scholars based in United States, United Kingdom and Austria. John Drewe's co-authors include Sui Xiong Cai, Ben Tseng, Shailaja Kasibhatla, William Kemnitzer, Songchun Jiang, Candace Crogan‐Grundy, Han‐Zhong Zhang, Rolf H. Joho, Henriette Gourdeau and Glenn H. Dillon and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

John Drewe

62 papers receiving 4.2k citations

Peers

Countries citing papers authored by John Drewe

Since Specialization

Citations

This map shows the geographic impact of John Drewe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by John Drewe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Drewe more than expected).

Fields of papers citing papers by John Drewe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John Drewe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by John Drewe. The network helps show where John Drewe may publish in the future.

Co-authorship network of co-authors of John Drewe

This figure shows the co-authorship network connecting the top 25 collaborators of John Drewe. A scholar is included among the top collaborators of John Drewe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with John Drewe. John Drewe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Cell-based apoptosis assays in oncology drug discovery 2010 ·Expert Opinion on Drug Discovery ·John Drewe, Sui Xiong Cai	8
2	Discovery of 4-Aryl-4H-Chromenes as Potent Apoptosis Inducers Using a Cell- and Caspase-Based Anti-Cancer Screening Apoptosis Program (ASAP): SAR Studies and the Identification of Novel Vascular Disrupting Agents 2009 ·Anti-Cancer Agents in Medicinal Chemistry ·Sui Xiong Cai, John Drewe, William Kemnitzer	88
3	Discovery of 3-aryl-5-aryl-1,2,4-oxadiazoles as a new series of apoptosis inducers. 2. Identification of more aqueous soluble analogs as potential anticancer agents 2009 ·Bioorganic & Medicinal Chemistry Letters ·William Kemnitzer, Jared Kuemmerle, Han‐Zhong Zhang, Shailaja Kasibhatla, Ben Tseng, John Drewe, Sui Xiong Cai	39
4	Discovery of substituted 4-anilino-2-arylpyrimidines as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. 2. Structure–activity relationships of the 2-aryl group 2009 ·Bioorganic & Medicinal Chemistry Letters ·Nilantha Sirisoma, Azra Pervin, Bao Nguyen, Candace Crogan‐Grundy, Shailaja Kasibhatla, Ben Tseng, John Drewe, Sui Xiong Cai	13
5	Discovery of N-aryl-9-oxo-9H-fluorene-1-carboxamides as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure–activity relationships of the 9-oxo-9H-fluorene ring 2009 ·Bioorganic & Medicinal Chemistry Letters ·William Kemnitzer, Nilantha Sirisoma, Songchun Jiang, Shailaja Kasibhatla, Candace Crogan‐Grundy, Ben Tseng, John Drewe, Sui Xiong Cai	21
6	Discovery of (naphthalen-4-yl)(phenyl)methanones and N-methyl-N-phenylnaphthalen-1-amines as new apoptosis inducers using a cell- and caspase-based HTS assay 2008 ·Bioorganic & Medicinal Chemistry Letters ·Songchun Jiang, Candace Crogan‐Grundy, John Drewe, Ben Tseng, Sui Xiong Cai	13
7	Selective activation of apoptosis by a novel set of 4-aryl-3-(3-aryl-1-oxo-2-propenyl)-2(1H)-quinolinones through a Myc-dependent pathway 2008 ·Cancer Letters ·Gisela Claassen, (unknown), Candace Crogan‐Grundy, Mei Vaillancourt, (unknown), Sui Xiong Cai, John Drewe, Ben Tseng, Shailaja Kasibhatla	65
8	Synthesis of caged 2,3,3a,7a-tetrahydro-3,6-methanobenzofuran-7(6H)-ones: Evaluating the minimum structure for apoptosis induction by gambogic acid 2008 ·Bioorganic & Medicinal Chemistry ·Jared Kuemmerle, Songchun Jiang, Ben Tseng, Shailaja Kasibhatla, John Drewe, Sui Xiong Cai	23
9	MPC-6827: A Small-Molecule Inhibitor of Microtubule Formation That Is Not a Substrate for Multidrug Resistance Pumps 2007 ·Cancer Research ·Shailaja Kasibhatla, Vijay Baichwal, Sui Xiong Cai, Bruce L. Roth, Ira Skvortsova, Sergej Skvortsov, Peter Lukáš, Nicole M. English, Nilantha Sirisoma, John Drewe, Azra Pervin, Ben Tseng, Robert Carlson, Christopher M. Pleiman	110
10	Discovery and structure–activity relationship of N-phenyl-1H-pyrazolo[3,4-b]quinolin-4-amines as a new series of potent apoptosis inducers 2007 ·Bioorganic & Medicinal Chemistry ·Han‐Zhong Zhang, Gisela Claassen, (unknown), Ben Tseng, John Drewe, Sui Xiong Cai	18
11	4-Aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay, structure-activity relationships of the 7, 8-positions 2006 ·Cancer Research ·Sui Xiong Cai, William Kemnitzer, Shailaja Kasibhatla, Songchun Jiang, (unknown), Ben Tseng, John Drewe, Denis Labrecque, Serge Lamothe, Henriette Gourdeau	2
12	A Chemical Genetics Approach for the Discovery of Apoptosis Inducers:From Phenotypic Cell Based HTS Assay and Structure-Activity Relationship Studies, to Identification of Potential Anticancer Agents and Molecular Targets. 2006 ·Current Medicinal Chemistry ·Chenglong Xiong, John Drewe, Shailaja Kasibhatla	58
13	Discovery of substituted 4-anilino-2-(2-pyridyl)pyrimidines as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. Part 1: Structure–activity relationships of the 4-anilino group 2006 ·Bioorganic & Medicinal Chemistry ·Nilantha Sirisoma, Shailaja Kasibhatla, Bao Nguyen, Azra Pervin, Yang Wang, Gisela Claassen, Ben Tseng, John Drewe, Sui Xiong Cai	38
14	The discovery and mechanism of action of novel tumor-selective and apoptosis-inducing 3,5-diaryl-1,2,4-oxadiazole series using a chemical genetics approach 2005 ·Molecular Cancer Therapeutics ·Katayoun A. Jessen, Nicole M. English, (unknown), Sergei Maliartchouk, (unknown), Ling Qiu, (unknown), Jared Kuemmerle, Han‐Zhong Zhang, Kurt R. Gehlsen, John Drewe, Ben Tseng, Sui Xiong Cai, Shailaja Kasibhatla	67
15	Discovery and SAR of indole-2-carboxylic acid benzylidene-hydrazides as a new series of potent apoptosis inducers using a cell-based HTS assay 2004 ·Bioorganic & Medicinal Chemistry ·Han‐Zhong Zhang, John Drewe, Ben Tseng, Shailaja Kasibhatla, Sui Xiong Cai	88
16	Pentylenetetrazole-induced inhibition of recombinant gamma-aminobutyric acid type A (GABA(A)) receptors: mechanism and site of action. 2001 ·PubMed ·(unknown), Cathy L. Bell-Horner, Mohammed Dibas, Douglas F. Covey, John Drewe, Glenn H. Dillon	292
17	Influence of subunit configuration on the interaction of picrotoxin-site ligands with recombinant GABAA receptors 2000 ·Molecular Brain Research ·Cathy L. Bell-Horner, Mohammed Dibas, Renqi Huang, John Drewe, Glenn H. Dillon	29
18	stable high expression of human gamma-aminobutyric acida receptors composed of alpha and beta subünitS 1995 ·Life Sciences ·John Drewe, Jie‐Sheng Chen, Antonio A. Reyes, Nancy C. Lan	4
19	Alteration and restoration of K+ channel function by deletions at the N- and C-termini 1990 ·Neuron ·Antonius M.J. VanDongen, Georges C. Frech, John Drewe, Rolf H. Joho, Arthur Brown	171
20	Synaptic Transmission Between Dissociated Adult Mammalian Neurons and Attached Synaptic Boutons 1988 ·Science ·John Drewe, Gwen V. Childs, Diana L. Kunze	48

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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