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Medicinal Chemistry

IF2.6
论文数19
被引数
期刊论文 19
发表时间
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Pyrimidine-Based Compounds in Tuberculosis Management: A Review of their Biological and Medicinal Importance嘧啶类化合物在结核病管理中的应用：对其生物和药理学重要性的综述
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deleteSingh, Deepshikha; Singh, Vikram; Moin, Afrasim; Gangadhar, Manu; Revanasiddappa, Bistuvalli Chandrashekarappa; Dixit, Sheshagiri R.
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Research Progress of G Protein-coupled Receptor 52 on Central Nervous System DiseasesG蛋白偶联受体52在神经系统疾病中的研究进展
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deleteWu, Qingkun; Li, Jun; Hu, Xiaojie; Zhuang, Ying; Zheng, Lu
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Curcumin-Based Virtual Screening Identifies Inhibitors of SARS-CoV-2 Spike Protein and ACE2 Receptor Binding
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IF2.6
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deleteDelgado-Maldonado, Timoteo; Gonzalez-Morales, Luis D.; Vargas-Salas, Gilberto; Rojas-Verde, Guadalupe; Ortiz-Perez, Eyra; Paz-Gonzalez, Alma D.; Rivera, Gildardo
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Exploring Pyridine-Based Schemes: A Comprehensive Review on their Synthesis and Therapeutic Applications探索吡啶类方案：关于其合成和 therapeutic applications 的综合评述
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deleteBalikai, Amruta M.; Kumar, M. R. Pradeep; Rajagopal, Kalirajan; Alshehri, Mohammed Ali; Rab, Safia Obaidur; Nafady, Mohamed H.; Emran, Talha Bin
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Expanding Therapeutic Horizons with Indazole-Based Compounds: A Review of Anticancer, Antimicrobial, and Neuroprotective Applications以吲唑类化合物拓展治疗视野：抗肿瘤、抗菌和神经保护应用的综述
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deleteBhane, Pooja Dinkar; Pawar, Sarita Suryabhan
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Synergistic Warriors: Design and Synthesis of Dual-Acting Schiff-Based Threaded 1,2,3-Triazole Hybrids for Potent Antineoplastic and Anti-Mycobacterial Activities协同战士：具有强效抗肿瘤和抗分枝杆菌活性的双作用席夫碱基互穿1,2,3-三唑杂化物的设计与合成
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deleteWalhekar, Vinayak; Kulkarni, Raghavendra; Nuli, Mohana Vamsi; Garige, Anil Kumar; Deore, Dharmesh; Pawar, Ritesh; Patil, Ashwini; Dvrn, Bhikshapathi; Santosh, Karajagi; Kulkarni, Ravindra
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Evaluating the Antitumor and Anti-inflammatory Efficacy of Natural Compounds Targeting TNFRs Using Computational Methods利用计算方法评估靶向TNFRs的天然化合物的抗肿瘤和抗炎功效
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deleteAkkaya, Hatice; Ozmaldar, Aydin
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Heterocyclic Derivatives in Parkinson's Therapy: Recent Advances and Prospects杂环衍生物在帕金森病治疗中的研究进展与展望
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deleteKanupriya, Vikram; Sharma, Vikram; Verma, Suraj Pal; Mishra, Isha; Mittal, Ravi K.; Biswas, Tanya; Mishra, Raghav
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Unlocking the Biological Potential of 2-Pyridones: Synthesis, Antioxidant and Antimicrobial Activity of N-Phenacylated 5/6-Chloro-2-pyridones解锁2-吡啶酮的生物潜力：N-苯乙酰基-5/6-氯-2-吡啶酮的合成、抗氧化和抗菌活性
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deleteSangwan, Sarita; Chauhan, Sonu; Yadav, Neelam; Kumar, Ravi; Duhan, Anil; Malik, Vinod; Sindhu, Jayant
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Novel Pyrrolopyrimidines as Inhibitors of CLK4 and HER2: Targeting Promising Anticancer Pathways新型吡咯并嘧啶作为CLK4和HER2的抑制剂：靶向有前景的抗肿瘤通路。Med. Chem. (Los. Angeles) 21, 1–11
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deleteGries, Jonathan; Totzke, Frank; Hilgeroth, Andreas
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Inhibitors of Phosphatidylinositol-specific Phospholipase C with Myo-inositol Scaffold肌醇骨架的磷脂酰肌醇特异性磷脂酶C抑制剂
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deleteBierkamp, Christian; Hanekamp, Walburga; Arenz, Christoph; Lehr, Matthias
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Exploring Recent Advances in the Pharmacological Activities of Pyrazole Compounds: A Comprehensive Review探索吡唑类化合物药理活性的最新进展：一篇综述
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deleteRaut, Kunal Ganesh; Chabukswar, Anuruddha Rajaram; Waghmare, Priyanka Sanjay; Jagdale, Swati Changdeo; Kachi, Onkar Gangaram; Pawar, Hari Ragho
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Design, Synthesis, and Biological Evaluation of a Novel Series of Thiazolidinediones as Dual GSK-3β and Tau Aggregation Inhibitors新型噻唑烷二酮系列的设计、合成及其作为GSK-3β和Tau聚集双重抑制剂的生物评价
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deleteAbdollahi, Zahra; Abnous, Khalil; Kalani, Mohamad Reza; Taghdisi, Seyed Mohammad; Soltani, Somaieh; Nejabat, Mojgan; Hadizadeh, Farzin
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Screening of Novel Inhibitors Targeting the Non-ATP-binding Domain of Staphylococcus aureus SecA1筛选靶向金黄色葡萄球菌SecA1非ATP结合域的新型抑制剂
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deleteLiu, Yan; Su, Qing; Wang, Zonglin; Liu, Peiyao; Hong, Jinjin; Seoh, Hyuk-kyu; Jia, Xu; Sui, Sen-Fang; Tai, Phang-Cheng; Huang, Xinhe
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Scaffold Hopping and Optimization of Thiazole Hybrids as Selective PIN1 Inhibitors: A Computational Study噻唑杂合物的骨架跳跃与优化作为选择性PIN1抑制剂的计算研究
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deleteChellappan, Meeramol C.; Vasu, Soumya; Mahadevan, Shriraam; Kathiravan, Muthu Kumaradoss; Jayaraman, Saravanan; Naik, Soniya; Thachil, Knolin K.
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Discovery of the PARP1 Inhibitors from Natural Compounds Using Structure-Based Virtual Screening and Bioactivity Evaluation基于结构虚拟筛选和生物活性评价从天然化合物中发现PARP1抑制剂
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deletePan, Dabo; Huang, Yaxuan; Jiang, Dewen; Jin, Xiaojie; Wu, Mingkai; Luo, Jianjun; Zhang, Yonghao
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Bioactive Compounds from Myrica esculenta: Antioxidant Insights and Docking Studies on H+K+-ATPase and H2 Receptor Targets从M. esculenta中分离的生物活性化合物：对H+K+-ATP酶和H2受体靶点的抗氧化见解与对接研究
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deletePathak, Rashmi; Chandra, Phool
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The Preface前言
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deleteHadjipavlou-Litina, Dimitra
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Recent Advances in Synthetic Pathways and Therapeutic Potential of Acridine and Acridone Derivatives吖啶和吖啶酮衍生物的合成路径及治疗潜力的最新进展
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deleteDalvi, Kalyani Asraji; Pawar, Sarita Suryabhan
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