Статті в журналах з теми "DPP Derivatives"
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Luo, Nan, Guanxin Zhang, and Zitong Liu. "Keep glowing and going: recent progress in diketopyrrolopyrrole synthesis towards organic optoelectronic materials." Organic Chemistry Frontiers 8, no. 16 (2021): 4560–81. http://dx.doi.org/10.1039/d1qo00613d.
Повний текст джерелаLeidel, Fabienne, Martin Eiden, Markus Geissen, Hans A. Kretzschmar, Armin Giese, Thomas Hirschberger, Paul Tavan, Hermann M. Schätzl, and Martin H. Groschup. "Diphenylpyrazole-Derived Compounds Increase Survival Time of Mice after Prion Infection." Antimicrobial Agents and Chemotherapy 55, no. 10 (July 11, 2011): 4774–81. http://dx.doi.org/10.1128/aac.00151-11.
Повний текст джерелаHe, Ran, Michael Forman, Bryan T. Mott, Rajkumar Venkatadri, Gary H. Posner, and Ravit Arav-Boger. "Unique and Highly Selective Anticytomegalovirus Activities of Artemisinin-Derived Dimer Diphenyl Phosphate Stem from Combination of Dimer Unit and a Diphenyl Phosphate Moiety." Antimicrobial Agents and Chemotherapy 57, no. 9 (June 17, 2013): 4208–14. http://dx.doi.org/10.1128/aac.00893-13.
Повний текст джерелаWang, Yu, Xialian Tang, and Lianghong Yi. "Design and Discovery of Novel 1,3,5-Triazines as Dipeptidyl Peptidase-4 Inhibitor against Diabetes." Pharmacology 103, no. 5-6 (2019): 273–81. http://dx.doi.org/10.1159/000494060.
Повний текст джерелаWang, Bing, Nannan He, Bo Li, Shuangying Jiang, Yi Qu, Sanyin Qu, and Jianli Hua. "Aggregation-Induced Emission and Large Two-Photon Absorption Cross-Sections of Diketopyrrolopyrrole (DPP) Derivatives." Australian Journal of Chemistry 65, no. 4 (2012): 387. http://dx.doi.org/10.1071/ch11410.
Повний текст джерелаWang, Lingyun, Bihong Lai, Xueguang Ran, Hao Tang, and Derong Cao. "Recent Advances of Diketopyrrolopyrrole Derivatives in Cancer Therapy and Imaging Applications." Molecules 28, no. 10 (May 15, 2023): 4097. http://dx.doi.org/10.3390/molecules28104097.
Повний текст джерелаYang, Sheng-Hsiung, and Chia-Hao Hsieh. "Novel Linear and Hyperbranched Polythiophene Derivatives Containing Diketopyrrolopyrroles as Linking Groups." MRS Proceedings 1771 (2015): 213–19. http://dx.doi.org/10.1557/opl.2015.497.
Повний текст джерелаSantoprete, Alessia, Elena Capitò, Paul E. Carrington, Alessandro Pocai, Marco Finotto, Annunziata Langella, Paolo Ingallinella, et al. "DPP-IV-resistant, long-acting oxyntomodulin derivatives." Journal of Peptide Science 17, no. 4 (February 3, 2011): 270–80. http://dx.doi.org/10.1002/psc.1328.
Повний текст джерелаKhalaf, Reema A., Dalal Masalha, and Dima Sabbah. "DPP-IV Inhibitory Phenanthridines: Ligand, Structure-Based Design and Synthesis." Current Computer-Aided Drug Design 16, no. 3 (June 2, 2020): 295–307. http://dx.doi.org/10.2174/1573409915666181211114743.
Повний текст джерелаIvanova, E. A., N. N. Zolotov, V. F. Pozdnev, and T. A. Voronina. "Effect of cyanopyrrolidine derivatives on the activity of prolylendopeptidase, acute exudative inflammation and visceral pain in mice." Biomeditsinskaya Khimiya 66, no. 1 (January 2020): 77–82. http://dx.doi.org/10.18097/pbmc20206601077.
Повний текст джерелаStas, Sara, Sergey Sergeyev, and Yves Geerts. "Synthesis of diketopyrrolopyrrole (DPP) derivatives comprising bithiophene moieties." Tetrahedron 66, no. 10 (March 2010): 1837–45. http://dx.doi.org/10.1016/j.tet.2010.01.027.
Повний текст джерелаSharma, Lisa, and Hugo Bronstein. "Synthesis of fully asymmetric diketopyrrolopyrrole derivatives." RSC Advances 11, no. 9 (2021): 5276–83. http://dx.doi.org/10.1039/d0ra01564d.
Повний текст джерелаFujii, Mikiya, Woong Shin, Takuma Yasuda, and Koichi Yamashita. "Photon-absorbing charge-bridging states in organic bulk heterojunctions consisting of diketopyrrolopyrrole derivatives and PCBM." Physical Chemistry Chemical Physics 18, no. 14 (2016): 9514–23. http://dx.doi.org/10.1039/c5cp06183k.
Повний текст джерелаYing, Shian, Mingshuai Chen, Zhongwei Liu, Kai Zhang, Yuyu Pan, Shanfeng Xue, and Wenjun Yang. "9-Anthryl-capped DPP-based dyes: aryl spacing induced differential optical properties." Journal of Materials Chemistry C 4, no. 34 (2016): 8006–13. http://dx.doi.org/10.1039/c6tc02761j.
Повний текст джерелаLi, Qing, Li Han, Bin Zhang, Jinpei Zhou, and Huibin Zhang. "Synthesis and biological evaluation of triazole based uracil derivatives as novel DPP-4 inhibitors." Organic & Biomolecular Chemistry 14, no. 40 (2016): 9598–611. http://dx.doi.org/10.1039/c6ob01818a.
Повний текст джерелаMusoev, Numonov, You, and Gao. "Discovery of Novel DPP-IV Inhibitors as Potential Candidates for the Treatment of Type 2 Diabetes mellitus Predicted by 3D QSAR Pharmacophore Models, Molecular Docking and de novo Evolution." Molecules 24, no. 16 (August 7, 2019): 2870. http://dx.doi.org/10.3390/molecules24162870.
Повний текст джерелаBidan, G., B. Divisia-Blohorn, M. Billon, J. M. Kern, and J. P. Sauvage. "Tangled 3-functionalized polypyrrole derivatives built around Cu(dpp)2+ (dpp = 2,9-diphenyl-1,10-phenanthroline)." Journal of Electroanalytical Chemistry 360, no. 1-2 (November 1993): 189–98. http://dx.doi.org/10.1016/0022-0728(93)87012-k.
Повний текст джерелаPatil, S., and R. Sharma. "INSIGHT INTO AMINOMETHYL-PIPERIDONES BASED DPP-IV INHIBITORS FOR TREATMENT OF DIABETES: AN APPLICATION OF RATIONAL DRUG DESIGN." INDIAN DRUGS 54, no. 04 (April 28, 2017): 5–21. http://dx.doi.org/10.53879/id.54.04.10808.
Повний текст джерелаKalli, Swarna Bharathi, and V. Velmurugan. "Design, synthesis and anti-diabetic activity of piperazine sulphonamide derivatives as dipeptidyl peptidase-4 inhibitors." Pharmacia 69, no. 4 (November 11, 2022): 987–93. http://dx.doi.org/10.3897/pharmacia.69.e95096.
Повний текст джерелаAbramić, Marija, and Dejan Agić. "Survey of Dipeptidyl Peptidase III Inhibitors: From Small Molecules of Microbial or Synthetic Origin to Aprotinin." Molecules 27, no. 9 (May 7, 2022): 3006. http://dx.doi.org/10.3390/molecules27093006.
Повний текст джерелаKhalaf, Reema Abu, Ghassan Abu Sheikha, Mahmoud Al-Sha'er, and Mutasem Taha. "Design, Synthesis and Biological Evaluation of N4-Sulfonamido-Succinamic, Phthalamic, Acrylic and Benzoyl Acetic Acid Derivatives as Potential DPP IV Inhibitors." Open Medicinal Chemistry Journal 7, no. 1 (November 29, 2013): 39–48. http://dx.doi.org/10.2174/1874104501307010039.
Повний текст джерелаWang, Xiaohua, Bin Jiang, Chenchen Du, Xiaolei Ren, Zhiming Duan, and Hongyu Wang. "Fluorinated dithienyl-diketopyrrolopyrrole: a new building block for organic optoelectronic materials." New Journal of Chemistry 43, no. 41 (2019): 16411–20. http://dx.doi.org/10.1039/c9nj04060a.
Повний текст джерелаSunil, Sreeja, Arul G. D. A. Smith, and Mathan S. "Design, Synthesis and Biological Evaluation of 2-Aminobenzimidazole Derivatives as DPP4 Inhibitors." Current Bioactive Compounds 16, no. 5 (July 16, 2020): 696–702. http://dx.doi.org/10.2174/1573407215666190318121902.
Повний текст джерелаVawhal, Pallavi Kishor, Shailaja B. Jadhav, Sumit Kaushik, Kahnu Charan Panigrahi, Chandan Nayak, Humaira Urmee, Sharuk L. Khan, et al. "Coumarin-Based Sulfonamide Derivatives as Potential DPP-IV Inhibitors: Pre-ADME Analysis, Toxicity Profile, Computational Analysis, and In Vitro Enzyme Assay." Molecules 28, no. 3 (January 19, 2023): 1004. http://dx.doi.org/10.3390/molecules28031004.
Повний текст джерелаSyam, Yasmin M., Somaia S. Abd El-Karim, Tamer Nasr, Samia A. Elseginy, Manal M. Anwar, Mohsen M. Kamel, and Hanan F. Ali. "Design, Synthesis and Biological Evaluation of Spiro Cyclohexane-1,2- Quinazoline Derivatives as Potent Dipeptidyl Peptidase IV Inhibitors." Mini-Reviews in Medicinal Chemistry 19, no. 3 (January 11, 2019): 250–69. http://dx.doi.org/10.2174/1389557517666170828121018.
Повний текст джерелаKhalaf, Reema Abu, Ebtisam Alwarafi, and Dima Sabbah. "Piperazine sulfonamides as DPP-IV inhibitors: Synthesis, induced-fit docking and in vitro biological evaluation." Acta Pharmaceutica 71, no. 4 (April 3, 2021): 631–43. http://dx.doi.org/10.2478/acph-2021-0034.
Повний текст джерелаYang, Ji, Haoqi Tan, Dongyu Li, Tao Jiang, Yuting Gao, Bo Li, Xue Qu, and Jianli Hua. "Synthesis, two-photon absorption and aggregation-induced emission properties of multi-branched triphenylamine derivatives based on diketopyrrolopyrrole for bioimaging." RSC Advances 6, no. 63 (2016): 58434–42. http://dx.doi.org/10.1039/c6ra11269b.
Повний текст джерелаBharath, D., S. Chithiravel, M. Sasikumar, Narendra Reddy Chereddy, Balaiah Shanigaram, K. Bhanuprakash, K. Krishnamoorthy та V. Jayathirtha Rao. "A detailed study on the thermal, photo-physical and electrochemical properties and OFET applications of D–π–A–π–D structured unsymmetrical diketopyrrolopyrrole materials". RSC Advances 5, № 115 (2015): 94859–65. http://dx.doi.org/10.1039/c5ra16653e.
Повний текст джерелаSong, Hao, Yao Gao, Weili Li, Hongkun Tian, Donghang Yan, Yanhou Geng, and Fosong Wang. "Synthesis and characterization of diketopyrrolopyrrole-based conjugated molecules flanked by indenothiophene and benzoindenothiophene derivatives." Journal of Materials Chemistry C 3, no. 42 (2015): 11135–43. http://dx.doi.org/10.1039/c5tc02288f.
Повний текст джерелаHwang, Tae Gyu, Jeong Yun Kim, Jin Woong Namgoong, Jae Moon Lee, Sim Bum Yuk, Se Hun Kim, and Jae Pil Kim. "Aggregation induced emission of diketopyrrolopyrrole (DPP) derivatives for highly fluorescent red films." Photochemical & Photobiological Sciences 18, no. 5 (2019): 1064–74. http://dx.doi.org/10.1039/c8pp00403j.
Повний текст джерелаYambulatov, Dmitriy S., Irina A. Lutsenko, Stanislav A. Nikolaevskii, Pavel A. Petrov, Ivan V. Smolyaninov, Irina K. Malyants, Victoria O. Shender та ін. "α-Diimine Cisplatin Derivatives: Synthesis, Structure, Cyclic Voltammetry and Cytotoxicity". Molecules 27, № 23 (5 грудня 2022): 8565. http://dx.doi.org/10.3390/molecules27238565.
Повний текст джерелаOgawa, Futa, Masanori Takeda, Kanae Miyanaga, Keita Tani, Ryuji Yamazawa, Kiyoshi Ito, Atsushi Tarui, Kazuyuki Sato, and Masaaki Omote. "Development of a fluorogenic small substrate for dipeptidyl peptidase-4." Beilstein Journal of Organic Chemistry 13 (December 14, 2017): 2690–97. http://dx.doi.org/10.3762/bjoc.13.267.
Повний текст джерелаHong, Lin, Bowen Zhou, Xiangxu Meng, Ding Zhang, Yihua Jiang, Dajun Liu, Guiqiu Wang, Jianli Hua та Yaochuan Wang. "Nonlinear Optical Properties of Several π Conjugated Bridge Groups based on Diketo-Pyrrole-Pyrrole: Study on the Length and Symmetry of N-atom Position Substituted Alkyl Chains". Journal of Physics: Conference Series 2470, № 1 (1 березня 2023): 012025. http://dx.doi.org/10.1088/1742-6596/2470/1/012025.
Повний текст джерелаLukina, Daria A., Alexandra A. Skatova, Anton N. Lukoyanov, Ekaterina A. Kozlova, and Igor L. Fedushkin. "Alkali metal reduction of 1,3,2-diazaborol and 1,3,2-diazagermol derivatives based on 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene." Dalton Transactions 49, no. 9 (2020): 2941–46. http://dx.doi.org/10.1039/c9dt04652f.
Повний текст джерелаJiang, Bin, Chen Chen Du, Min Jie Li, Ke Gao, Li Kou, Ming Chen, Feng Liu, Thomas P. Russell, and Hongyu Wang. "Synthesis of fluorinated diphenyl-diketopyrrolopyrrole derivatives as new building blocks for conjugated copolymers." Polymer Chemistry 7, no. 19 (2016): 3311–24. http://dx.doi.org/10.1039/c6py00346j.
Повний текст джерелаPeriasamy, Mariappan, Boda Venkanna, Miriyala Nagaraju, and Lakavathu Mohan. "Methods for the Synthesis of Piperazine Derivatives Containing a Chiral Bi-2-naphthyl Moiety." Synthesis 52, no. 01 (October 1, 2019): 127–34. http://dx.doi.org/10.1055/s-0037-1610731.
Повний текст джерелаPark, Woul Seong, Mi Ae Jun, Mi Sik Shin, Sung Wook Kwon, Seung Kyu Kang, Ki Young Kim, Sang Dal Rhee, et al. "Synthesis and biological evaluation of triazepane derivatives as DPP-IV inhibitors." Journal of Fluorine Chemistry 130, no. 11 (November 2009): 1001–10. http://dx.doi.org/10.1016/j.jfluchem.2009.08.001.
Повний текст джерелаBura, Thomas, Serge Beaupré, Marc-André Légaré, Olzhas Ibraikulov, Nicolas Leclerc, and Mario Leclerc. "Theoretical Calculations for Highly Selective Direct Heteroarylation Polymerization: New Nitrile-Substituted Dithienyl-Diketopyrrolopyrrole-Based Polymers." Molecules 23, no. 9 (September 12, 2018): 2324. http://dx.doi.org/10.3390/molecules23092324.
Повний текст джерелаBelal, Fathalla, Ibrahim A. Al-Zaagi, and Mohamed A. Abounassif. "Voltammetric Determination of Benazepril and Ramipril in Dosage Forms and Biological Fluids through Nitrosation." Journal of AOAC INTERNATIONAL 84, no. 1 (January 1, 2001): 1–8. http://dx.doi.org/10.1093/jaoac/84.1.1.
Повний текст джерелаSannes, P. L., B. H. Schofield, and D. F. McDonald. "Histochemical localization of cathepsin B, dipeptidyl peptidase I, and dipeptidyl peptidase II in rat bone." Journal of Histochemistry & Cytochemistry 34, no. 8 (August 1986): 983–88. http://dx.doi.org/10.1177/34.8.3016074.
Повний текст джерелаAgrawal, Ritesh, Pratima Jain, Subodh Dikshit, and Radhe Bahare. "3D QSAR and Docking Study of Gliptin Derivatives as DPP-IV Inhibitors." Combinatorial Chemistry & High Throughput Screening 16, no. 4 (February 1, 2013): 249–73. http://dx.doi.org/10.2174/1386207311316040001.
Повний текст джерелаHan, Bei, Jing Long Liu, Yi Huan, Peng Li, Qi Wu, Zi Yun Lin, Zhu Fang Shen, Da Li Yin, and Hai Hong Huang. "Design, synthesis and primary activity of thiomorpholine derivatives as DPP-IV inhibitors." Chinese Chemical Letters 23, no. 3 (March 2012): 297–300. http://dx.doi.org/10.1016/j.cclet.2011.12.007.
Повний текст джерелаAreephong, Jetsuda, Arthur D. Hendsbee та Gregory C. Welch. "Facile synthesis of unsymmetrical and π-extended furan-diketopyrrolopyrrole derivatives through C–H direct (hetero)arylation using a heterogeneous catalyst system". New Journal of Chemistry 39, № 9 (2015): 6714–17. http://dx.doi.org/10.1039/c5nj01150g.
Повний текст джерелаEmami, Leila, Zahra Faghih, Amirhossein Sakhteman, Zahra Rezaei, Zeinab Faghih, Farnaz Salehi, and Soghra Khabnadideh. "Design, synthesis, molecular simulation, and biological activities of novel quinazolinone-pyrimidine hybrid derivatives as dipeptidyl peptidase-4 inhibitors and anticancer agents." New Journal of Chemistry 44, no. 45 (2020): 19515–31. http://dx.doi.org/10.1039/d0nj03774e.
Повний текст джерелаSong, Xuejing, Lingqian Kong, Hongmei Du, Xiangyu Li, Hanlin Feng, Jinsheng Zhao, and Yu Xie. "Effects of Pyrazine Derivatives and Substituted Positions on the Photoelectric Properties and Electromemory Performance of D–A–D Series Compounds." Materials 11, no. 10 (October 22, 2018): 2063. http://dx.doi.org/10.3390/ma11102063.
Повний текст джерелаAgić, Dejan, Maja Karnaš, Domagoj Šubarić, Melita Lončarić, Sanja Tomić, Zrinka Karačić, Drago Bešlo, et al. "Coumarin Derivatives Act as Novel Inhibitors of Human Dipeptidyl Peptidase III: Combined In Vitro and In Silico Study." Pharmaceuticals 14, no. 6 (June 5, 2021): 540. http://dx.doi.org/10.3390/ph14060540.
Повний текст джерелаLi, Ning, Li-Jun Wang, Bo Jiang, Shu-Ju Guo, Xiang-Qian Li, Xue-Chun Chen, Jiao Luo, Chao Li, Yi Wang, and Da-Yong Shi. "Design, synthesis and biological evaluation of novel pyrimidinedione derivatives as DPP-4 inhibitors." Bioorganic & Medicinal Chemistry Letters 28, no. 12 (July 2018): 2131–35. http://dx.doi.org/10.1016/j.bmcl.2018.05.022.
Повний текст джерелаGuild, Jonathan, Michael J. Morris, Craig C. Robertson, and Alexander W. H. Speed. "One-pot synthesis of new iso-DPP derivatives from terminal alkynes and isocyanates." Tetrahedron Letters 60, no. 39 (September 2019): 151079. http://dx.doi.org/10.1016/j.tetlet.2019.151079.
Повний текст джерелаSoni, Rina, and Shubhangi S. Soman. "Design and synthesis of aminocoumarin derivatives as DPP-IV inhibitors and anticancer agents." Bioorganic Chemistry 79 (September 2018): 277–84. http://dx.doi.org/10.1016/j.bioorg.2018.05.008.
Повний текст джерелаFang, Yuanying, Shaokun Zhang, Wenting Wu, Yanhua Liu, Juan Yang, Yuyuan Li, Min Li, et al. "Design and synthesis of tetrahydropyridopyrimidine derivatives as dual GPR119 and DPP-4 modulators." Bioorganic Chemistry 94 (January 2020): 103390. http://dx.doi.org/10.1016/j.bioorg.2019.103390.
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