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ACS Chemical Neuroscience
|
July 11, 2012
The "specific" P-glycoprotein inhibitor Tariquidar is also a substrate and an inhibitor for breast cancer resistance protein (BCRP/ABCG2)
Pavitra Kannan, Sanjay Telu, Suneet Shukla, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
January 18, 2023
Broad-scope Syntheses of [<sup>11</sup> C/<sup>18</sup> F]Trifluoromethylarenes from Aryl(mesityl)iodonium Salts
Sanjay Telu, Susovan Jana, Mohammad B Haskali, et al.
RSC Medicinal Chemistry
|
January 22, 2021
Syntheses of [<sup>11</sup>C]2- and [<sup>11</sup>C]3-trifluoromethyl-4-aminopyridine: potential PET radioligands for demyelinating diseases
Karla M Ramos-Torres, Yu-Peng Zhou, Bo Yeun Yang, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
November 19, 2016
11C-ER176, a Radioligand for 18-kDa Translocator Protein, Has Adequate Sensitivity to Robustly Image All Three Affinity Genotypes in Human Brain
Masamichi Ikawa, Talakad G Lohith, Stal Shrestha, et al.
EJNMMI Research
|
April 5, 2023
Candidate 3-benzazepine-1-ol type GluN2B receptor radioligands (<sup>11</sup>C-NR2B-Me enantiomers) have high binding in cerebellum but not to σ1 receptors
Lisheng Cai, Jeih-San Liow, Cheryl L Morse, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
March 22, 2017
<sup>11</sup>C-DPA-713 has much greater specific binding to translocator protein 18 kDa (TSPO) in human brain than <sup>11</sup>C-( R)-PK11195
Masato Kobayashi, Teresa Jiang, Sanjay Telu, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
January 12, 2020
Evaluation of <sup>11</sup>C-NR2B-SMe and Its Enantiomers as PET Radioligands for Imaging the NR2B Subunit Within the NMDA Receptor Complex in Rats
Lisheng Cai, Jeih-San Liow, Cheryl L Morse, et al.
EJNMMI Research
|
October 18, 2017
Comparison of four <sup>11</sup>C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176-based on recent publications that measured specific-to-non-displaceable ratios
Masahiro Fujita, Masato Kobayashi, Masamichi Ikawa, et al.
ACS Chemical Neuroscience
|
January 2, 2025
Development and Evaluation in Rat and Monkey of a Candidate Homochiral Radioligand for PET Studies of Brain Receptor Interacting Protein Kinase 1: [<sup>18</sup>F](<i>S</i>)-1-(5-(3-Fluorophenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)-2,2-dimethylpropan-1-one
Susovan Jana, Mudasir Maqbool, Xuefeng Yan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 26, 2011
Lysosomal trapping of a radiolabeled substrate of P-glycoprotein as a mechanism for signal amplification in PET
Pavitra Kannan, Kyle R Brimacombe, William C Kreisl, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 48) with videos related to
Sort By:
Page
of 5
ACS Chemical Neuroscience
|
July 11, 2012
The "specific" P-glycoprotein inhibitor Tariquidar is also a substrate and an inhibitor for breast cancer resistance protein (BCRP/ABCG2)
Pavitra Kannan, Sanjay Telu, Suneet Shukla, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
January 18, 2023
Broad-scope Syntheses of [<sup>11</sup> C/<sup>18</sup> F]Trifluoromethylarenes from Aryl(mesityl)iodonium Salts
Sanjay Telu, Susovan Jana, Mohammad B Haskali, et al.
RSC Medicinal Chemistry
|
January 22, 2021
Syntheses of [<sup>11</sup>C]2- and [<sup>11</sup>C]3-trifluoromethyl-4-aminopyridine: potential PET radioligands for demyelinating diseases
Karla M Ramos-Torres, Yu-Peng Zhou, Bo Yeun Yang, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
November 19, 2016
11C-ER176, a Radioligand for 18-kDa Translocator Protein, Has Adequate Sensitivity to Robustly Image All Three Affinity Genotypes in Human Brain
Masamichi Ikawa, Talakad G Lohith, Stal Shrestha, et al.
EJNMMI Research
|
April 5, 2023
Candidate 3-benzazepine-1-ol type GluN2B receptor radioligands (<sup>11</sup>C-NR2B-Me enantiomers) have high binding in cerebellum but not to σ1 receptors
Lisheng Cai, Jeih-San Liow, Cheryl L Morse, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
March 22, 2017
<sup>11</sup>C-DPA-713 has much greater specific binding to translocator protein 18 kDa (TSPO) in human brain than <sup>11</sup>C-( R)-PK11195
Masato Kobayashi, Teresa Jiang, Sanjay Telu, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
January 12, 2020
Evaluation of <sup>11</sup>C-NR2B-SMe and Its Enantiomers as PET Radioligands for Imaging the NR2B Subunit Within the NMDA Receptor Complex in Rats
Lisheng Cai, Jeih-San Liow, Cheryl L Morse, et al.
EJNMMI Research
|
October 18, 2017
Comparison of four <sup>11</sup>C-labeled PET ligands to quantify translocator protein 18 kDa (TSPO) in human brain: (R)-PK11195, PBR28, DPA-713, and ER176-based on recent publications that measured specific-to-non-displaceable ratios
Masahiro Fujita, Masato Kobayashi, Masamichi Ikawa, et al.
ACS Chemical Neuroscience
|
January 2, 2025
Development and Evaluation in Rat and Monkey of a Candidate Homochiral Radioligand for PET Studies of Brain Receptor Interacting Protein Kinase 1: [<sup>18</sup>F](<i>S</i>)-1-(5-(3-Fluorophenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl)-2,2-dimethylpropan-1-one
Susovan Jana, Mudasir Maqbool, Xuefeng Yan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 26, 2011
Lysosomal trapping of a radiolabeled substrate of P-glycoprotein as a mechanism for signal amplification in PET
Pavitra Kannan, Kyle R Brimacombe, William C Kreisl, et al.
Page
of 5