日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Design, Synthesis, and Anti-RNA Virus Activity of 6'-Fluorinated-Aristeromycin Analogues

6'-氟代阿利司霉素类似物的设计、合成及抗RNA病毒活性

期刊:Journal of Medicinal Chemistry
影响因子:6.8
doi:10.1021/acs.jmedchem.9b00781
Yoon, Ji-Seong; Kim, Gyudong; Jarhad, Dnyandev B; Kim, Hong-Rae; Shin, Young-Sup; Qu, Shuhao; Sahu, Pramod K; Kim, Hea Ok; Lee, Hyuk Woo; Wang, Su Bin; Kong, Yun Jeong; Chang, Tong-Shin; Ogando, Natacha S; Kovacikova, Kristina; Snijder, Eric J; Posthuma, Clara C; van Hemert, Martijn J; Jeong, Lak Shin
微生物学
发表日期：2019
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Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists.

构象锁定截短的 2-己炔基-N(6)-取代-(N)-甲氧基碳核苷作为 A3 腺苷受体拮抗剂和部分激动剂的合成及其抗肾纤维化活性

期刊:Journal of Medicinal Chemistry
影响因子:6.8
doi:10.1021/jm4015313
Nayak Akshata, Chandra Girish, Hwang Inah, Kim Kyunglim, Hou Xiyan, Kim Hea Ok, Sahu Pramod K, Roy Kuldeep K, Yoo Jakyung, Lee Yoonji, Cui Minghua, Choi Sun, Moss Steven M, Phan Khai, Gao Zhan-Guo, Ha Hunjoo, Jacobson Kenneth A, Jeong Lak Shin
其它
发表日期：2014
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Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-N,N-dialkyluronamides as human A3 adenosine receptor antagonists

2-氯-N6-取代-4'-硫代腺苷-5'-N,N-二烷基糖醛酸酰胺作为人A3腺苷受体拮抗剂的构效关系

期刊:Bioorganic & Medicinal Chemistry Letters
影响因子:2.2
doi:10.1016/j.bmcl.2008.01.070
Jeong, Lak Shin; Lee, Hyuk Woo; Kim, Hea Ok; Tosh, Dilip K; Pal, Shantanu; Choi, Won Jun; Gao, Zhan-Guo; Patel, Amit R; Williams, Wanda; Jacobson, Kenneth A; Kim, Hee-Doo
信号转导
发表日期：2008
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Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides

利用定制核苷探测经改造以实现正交识别的A1腺苷受体的结合位点

期刊:Biochemistry
影响因子:3
doi:10.1021/bi7001828
Palaniappan, Krishnan K; Gao, Zhan-Guo; Ivanov, Andrei A; Greaves, Rebecca; Adachi, Hayamitsu; Besada, Pedro; Kim, Hea Ok; Kim, Ae Yil; Choe, Seung Ah; Jeong, Lak Shin; Jacobson, Kenneth A
信号转导
发表日期：2007
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Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5'-ribofuran-uronamide moiety

通过修饰 5'-核糖呋喃-尿酰胺部分将 A3 腺苷受体激动剂转化为选择性拮抗剂

期刊:Bioorganic & Medicinal Chemistry Letters
影响因子:2.2
doi:10.1016/j.bmcl.2005.10.054
Gao, Zhan-Guo; Joshi, Bhalchandra V; Klutz, Athena M; Kim, Soo-Kyung; Lee, Hyuk Woo; Kim, Hea Ok; Jeong, Lak Shin; Jacobson, Kenneth A
信号转导
发表日期：2006
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Design and synthesis of 3'-ureidoadenosine-5'-uronamides: effects of the 3'-ureido group on binding to the A3 adenosine receptor

3'-脲基腺苷-5'-尿酰胺的设计与合成：3'-脲基对与A3腺苷受体结合的影响

期刊:Bioorganic & Medicinal Chemistry Letters
影响因子:2.2
doi:10.1016/j.bmcl.2004.07.042
Jeong, Lak Shin; Kim, Myong Jung; Kim, Hea Ok; Gao, Zhan-Guo; Kim, Soo-Kyung; Jacobson, Kenneth A; Chun, Moon Woo
信号转导
发表日期：2004
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Design, synthesis and binding affinity of 3'-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands

Cl-IB-MECA 的 3'-氟类似物作为腺苷 A3 受体配体的设计、合成和结合亲和力

期刊:Bioorganic & Medicinal Chemistry Letters
影响因子:2.2
doi:10.1016/s0960-894x(03)00027-1
Lim, Moo Hong; Kim, Hea Ok; Moon, Hyung Ryong; Lee, Seung Jin; Chun, Moon Woo; Gao, Zhan-Guo; Melman, Neli; Jacobson, Kenneth A; Kim, Joong Hyup; Jeong, Lak Shin
信号转导
发表日期：2003
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Activation and Desensitization of Rat A(3)-Adenosine Receptors by Selective Adenosine Derivatives and Xanthine-7-Ribosides

选择性腺苷衍生物和黄嘌呤-7-核苷对大鼠A(3)-腺苷受体的激活和脱敏作用

期刊:Drug Development Research
影响因子:4.2
doi:10.1002/(SICI)1098-2299(199806/07)44:2/3<97::AID-DDR7>3.0.CO;2-5
Park, Kyung-Sun; Hoffmann, Carsten; Kim, Hea Ok; Padgett, William L; Daly, John W; Brambilla, Roberta; Motta, Cristina; Abbracchio, Maria P; Jacobson, Kenneth A
信号转导
Rat
免疫/内分泌
发表日期：1998
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