Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Xiangshu Fei"'
Autor:
Qi Huang Zheng, Xiangshu Fei
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 28:939-945
New radiolabeled matrix metalloproteinase inhibitors (MMPIs) [11C]Me‐Halo‐CGS 27023A analogs have been synthesized for evaluation as potential novel positron emission tomography (PET) tumor imaging agents. Their lipophilicity coefficients (log P)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::689db32df38a6806550f68b492fcf802
https://doi.org/10.1081/jlc-200051486
https://doi.org/10.1081/jlc-200051486
Autor:
Xiangshu Fei, Qi Huang Zheng, Barbara E. Glick-Wilson, Michael L. Sullivan, Ji Quari Wang, Gary D. Hutchins, Bruce H. Mock, Timothy R. DeGrado
Publikováno v:
Synthetic Communications. 34:1897-1907
An improved synthesis of [11C]raclopride is reported. The precursor desmethyl‐raclopride was synthesized from 3,5‐dichloro‐2,6‐dimethoxybenzoic acid and (S)‐(−)‐2‐aminoethyl‐1‐ethylpyrrolidine via a straightforward, four‐step sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e67fd73010774c126e1912c299b135a
https://doi.org/10.1081/scc-120034174
https://doi.org/10.1081/scc-120034174
Autor:
Qi Huang Zheng, Xuan Liu, Michael L. Sullivan, Barbara E. Glick-Wilson, Ji Quan Wang, Thomas A. Gardner, Sudhanshu P. Raikwar, Bruce H. Mock, Xiangshu Fei, Chinghai Kao, Gary D. Hutchins
Publikováno v:
Synthetic Communications. 34:917-932
An improved total synthesis of [18F]FHPG starting from 1,3‐dibenzyloxy‐2‐propanol and guanine has been developed. [18F]FHPG was prepared by nucleophilic substitution of the appropriate precursor with [18F]KF/Kryptofix 2.2.2 followed by a quick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f82e7ce86377286baa842b6dd17cf5ff
https://doi.org/10.1081/scc-120028365
https://doi.org/10.1081/scc-120028365
Autor:
Xuan Liu, Barbara E. Glick-Wilson, Bruce H. Mock, Michael L. Sullivan, Xiangshu Fei, Gary D. Hutchins, Ji Quan Wang, Thomas A. Gardner, Sudhanshu P. Raikwar, Qi Huang Zheng, Chinghai Kao
Publikováno v:
Synthetic Communications. 34:689-704
An improved total synthesis of [18F]FHBG starting from triethyl‐1,1,2‐ethanetricarboxylate and 2‐amino‐6‐chloropurine is reported. [18F]FHBG was prepared by nucleophilic substitution of the appropriate precursor with [18F]KF/Kryptofix 2.2.2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17c155dc5e40268df670094d699a7aeb
https://doi.org/10.1081/scc-120027717
https://doi.org/10.1081/scc-120027717
Autor:
George W. Sledge, Gary D. Hutchins, Kathy D. Miller, Xiangshu Fei, Qi Huang Zheng, Ji Quan Wang
Publikováno v:
Nuclear Medicine and Biology. 31:1033-1041
Xeloda (Capecitabine), a prodrug of antitumor agent 5-fluorouracil, is the first and only oral fluoropyrimidine to be approved for use as second-line therapy in metastatic breast cancer, colorectal cancer, and other solid malignancies. Fluorine-18 la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9deeca445072d726dc87ff4a4fd0ec6c
https://doi.org/10.1016/j.nucmedbio.2004.02.006
https://doi.org/10.1016/j.nucmedbio.2004.02.006
Autor:
William J. Groh, John C. Lopshire, Gary D. Hutchins, Douglas P. Zipes, Michael A. Miller, K. Lee Stone, Qi Huang Zheng, Xiangshu Fei, Ji Quan Wang
Publikováno v:
Nuclear Medicine and Biology. 31:957-964
A series of 11C-labeled analogs of the acetylcholinesterase (AChE) inhibitor pyridostigmine have been synthesized for evaluation as new potential positron emission tomography (PET) imaging agents for heart AChE. The appropriate precursors for radiola
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df2c6179f73df81e55425245b3e6a29
https://doi.org/10.1016/j.nucmedbio.2004.04.005
https://doi.org/10.1016/j.nucmedbio.2004.04.005
Synthesis, biodistribution and micro-PET imaging of radiolabeled antimitotic agent T138067 analogues
Autor:
K. Lee Stone, Tanya D. Martinez, Qi Huang Zheng, Xiangshu Fei, Kathy D. Miller, George W. Sledge, Gary D. Hutchins, Ji Quan Wang
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:1247-1251
Radiolabeled antimitotic agents [11C]T138067 and [18F]T138067 have been synthesized for evaluation as new potential positron emission tomography (PET) biomarkers for cancer imaging. In vivo biodistribution and micro-PET imaging of [11C]T138067 were p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53c0afe3193e1d29c061d8be8d801a6
https://doi.org/10.1016/j.bmcl.2003.12.061
https://doi.org/10.1016/j.bmcl.2003.12.061
Autor:
Qi-Huang Zheng, Xiangshu Fei, Xuan Liu, Ji-Quan Wang, K Lee Stone, Tanya D Martinez, Dawn J Gay, Winston L Baity, Kathy D Miller, George W Sledge, Gary D Hutchins
Publikováno v:
Nuclear Medicine and Biology. 31:77-85
(S)-2-(4'-[11C]methoxybiphenyl-4-sulfonylamino)-3-methylbutyric acid ([11C]MSMA) and N-hydroxy-(R)-2-[[(4'-[11C]methoxyphenyl)sulfonyl]benzylamino]-3-methylbutanamide ([11C]CGS 25966), carbon-11 labeled matrix metalloproteinase (MMP) inhibitors, have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4db8c4d685c16005b40fa8ab349e22c8
https://doi.org/10.1016/s0969-8051(03)00111-2
https://doi.org/10.1016/s0969-8051(03)00111-2
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:3933-3938
Positron emission tomography (PET) herpes simplex virus thymidine kinase (HSV-tk) gene reporter probes 9-[(3-[18F]fluoro-1-hydroxy-2-propoxy)methyl]guanine ([18F]FHPG) and 9-(4-[18F]fluoro-3-hydroxymethylbutyl)guanine ([18F]FHBG) were prepared by nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9126ce1ce8306f057d62e031321100ff
https://doi.org/10.1016/j.bmcl.2003.09.010
https://doi.org/10.1016/j.bmcl.2003.09.010
Autor:
Qi-Huang Zheng, Xiangshu Fei, Timothy R DeGrado, Ji-Quan Wang, K Lee Stone, Tanya D Martinez, Dawn J Gay, Winston L Baity, Bruce H Mock, Barbara E Glick-Wilson, Michael L Sullivan, Kathy D Miller, George W Sledge, Gary D Hutchins
Publikováno v:
Nuclear Medicine and Biology. 30:753-760
(2R)-2-[[4-(6-fluorohex-1-ynyl)phenyl]sulfonylamino]-3-methylbutyric acid [(11)C]methyl ester ([(11)C]FMAME), a novel carbon-11 labeled matrix metalloproteinase (MMP) inhibitor, has been synthesized for evaluation as new potential positron emission t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::885975b5c8ce6287a9c8736ba58553cd
https://doi.org/10.1016/s0969-8051(03)00086-6
https://doi.org/10.1016/s0969-8051(03)00086-6