Статті в журналах з теми "QSAR Model"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "QSAR Model".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Li, Yan Kun, and Xiao Ying Ma. "QSAR/QSPR Model Research of Complicated Samples." Advanced Materials Research 740 (August 2013): 306–9. http://dx.doi.org/10.4028/www.scientific.net/amr.740.306.
Повний текст джерелаOkey, Robert W., and H. David Stensel. "A QSAR-based biodegradability model—A QSBR." Water Research 30, no. 9 (September 1996): 2206–14. http://dx.doi.org/10.1016/0043-1354(96)00098-x.
Повний текст джерелаZhang, Xiujun, H. G. Govardhana Reddy, Arcot Usha, M. C. Shanmukha, Mohammad Reza Farahani, and Mehdi Alaeiyan. "A study on anti-malaria drugs using degree-based topological indices through QSPR analysis." Mathematical Biosciences and Engineering 20, no. 2 (2022): 3594–609. http://dx.doi.org/10.3934/mbe.2023167.
Повний текст джерелаToropov, Andrey A., and Alla P. Toropova. "The Monte Carlo Method as a Tool to Build up Predictive QSPR/QSAR." Current Computer-Aided Drug Design 16, no. 3 (June 2, 2020): 197–206. http://dx.doi.org/10.2174/1573409915666190328123112.
Повний текст джерелаMudasir, Mudasir, Iqmal Tahir, and Ida Puji Astuti Maryono Putri. "QUANTITATIVE STRUCTURE AND ACTIVITY RELATIONSHIP ANALYSIS OF 1,2,4-THIADIAZOLINE FUNGICIDES BASED ON MOLECULAR STRUCTURE CALCULATED BY AM1 METHOD." Indonesian Journal of Chemistry 3, no. 1 (June 7, 2010): 39–47. http://dx.doi.org/10.22146/ijc.21904.
Повний текст джерелаSarkar, Bikash Kumar. "DFT Based QSAR Studies of Phenyl Triazolinones of Protoporphyrinogen Oxidase Inhibitors." Asian Journal of Organic & Medicinal Chemistry 5, no. 4 (December 31, 2020): 307–11. http://dx.doi.org/10.14233/ajomc.2020.ajomc-p280.
Повний текст джерелаRybińska-Fryca, Anna, Anita Sosnowska, and Tomasz Puzyn. "Representation of the Structure—A Key Point of Building QSAR/QSPR Models for Ionic Liquids." Materials 13, no. 11 (May 30, 2020): 2500. http://dx.doi.org/10.3390/ma13112500.
Повний текст джерелаPokle, Maithili S., Rashmi D. Singh, and Madhura P. Vaidya. "2D QSAR MODEL BASED ON 1,2-DISUBSTITUTED BENZIMIDAZOLES IMPDH INHIBITORS." Indian Drugs 59, no. 04 (June 1, 2022): 18–23. http://dx.doi.org/10.53879/id.59.04.13117.
Повний текст джерелаBu, Qingwei, Qingshan Li, Yun Liu, and Chun Cai. "Performance Comparison between the Specific and Baseline Prediction Models of Ecotoxicity for Pharmaceuticals: Is a Specific QSAR Model Inevitable?" Journal of Chemistry 2021 (October 31, 2021): 1–8. http://dx.doi.org/10.1155/2021/5563066.
Повний текст джерелаLIAO, SI YAN, LI QIAN, JIN CAN CHEN, YONG SHEN, and KANG CHENG ZHENG. "2D/3D-QSAR STUDY ON ANALOGUES OF 2-METHOXYESTRADIOL WITH ANTICANCER ACTIVITY." Journal of Theoretical and Computational Chemistry 07, no. 02 (April 2008): 287–301. http://dx.doi.org/10.1142/s0219633608003745.
Повний текст джерелаZhao, Manman, Lin Wang, Linfeng Zheng, Mengying Zhang, Chun Qiu, Yuhui Zhang, Dongshu Du, and Bing Niu. "2D-QSAR and 3D-QSAR Analyses for EGFR Inhibitors." BioMed Research International 2017 (2017): 1–11. http://dx.doi.org/10.1155/2017/4649191.
Повний текст джерелаPapa, Ester, Alessandro Sangion, Olivier Taboureau, and Paola Gramatica. "Quantitative Prediction of Rat Hepatotoxicity by Molecular Structure." International Journal of Quantitative Structure-Property Relationships 3, no. 2 (July 2018): 49–60. http://dx.doi.org/10.4018/ijqspr.2018070104.
Повний текст джерелаVries, D., B. A. Wols, and P. de Voogt. "Removal efficiency calculated beforehand: QSAR enabled predictions for nanofiltration and advanced oxidation." Water Supply 13, no. 6 (September 13, 2013): 1425–36. http://dx.doi.org/10.2166/ws.2013.109.
Повний текст джерелаTosato, Maria Livia, Claudio Chiorboli, Lennart Eriksson, Jorgen Jonsson, Silvia Marchini, Laura Passerini, Anna Pino, and Luigi Viganó. "Quantitative Structure—Activity Relationships (QSARs): An Integrated Multivariate Approach for Risk Assessment Studies." Journal of the American College of Toxicology 9, no. 6 (November 1990): 629–38. http://dx.doi.org/10.3109/10915819009078768.
Повний текст джерелаGombar, Vijay K., Harold H. Borgstedt, Kurt Enslein, Jeffrey B. Hart, and Benjamin W. Blake. "A QSAR Model of Teratogenesis." Quantitative Structure-Activity Relationships 10, no. 4 (1991): 306–32. http://dx.doi.org/10.1002/qsar.19910100404.
Повний текст джерелаRaevsky, Oleg, Alexei Sapegin, and Nikolai Zefirov. "The QSAR Discriminant-Regression Model." QSAR & Combinatorial Science 13, no. 4 (1994): 412–18. http://dx.doi.org/10.1002/qsar.19940130406.
Повний текст джерелаKuz’min, Victor E., Anatoly G. Artemenko, Nikolay A. Kovdienko, Igor V. Tetko, and David J. Livingstone. "Lattice Model for QSAR Studies." Journal of Molecular Modeling 6, no. 7-8 (August 2000): 517–26. http://dx.doi.org/10.1007/s0089400060517.
Повний текст джерелаNAZİB ALİAS, Ahmad, and Zubainun MOHAMED ZABİDİ. "QSAR Studies on Nitrobenzene Derivatives using Hyperpolarizability and Conductor like Screening model as Molecular Descriptors." Journal of the Turkish Chemical Society Section A: Chemistry 9, no. 3 (August 31, 2022): 953–68. http://dx.doi.org/10.18596/jotcsa.1083840.
Повний текст джерелаT. Stanton, David. "QSAR and QSPR Model Interpretation Using Partial Least Squares (PLS) Analysis." Current Computer Aided-Drug Design 8, no. 2 (April 1, 2012): 107–27. http://dx.doi.org/10.2174/157340912800492357.
Повний текст джерелаSong, Xiaoying, Gaoya Wen, and Li Chai. "Graph signal processing based nonlinear QSAR/QSPR model learning for compounds." Biomedical Signal Processing and Control 91 (May 2024): 106011. http://dx.doi.org/10.1016/j.bspc.2024.106011.
Повний текст джерелаMudasir, Mudasir, Yari Mukti Wibowo, and Harno Dwi Pranowo. "Design of New Potent Insecticides of Organophosphate Derivatives Based on QSAR Analysis." Indonesian Journal of Chemistry 13, no. 1 (May 6, 2013): 86–93. http://dx.doi.org/10.22146/ijc.21331.
Повний текст джерелаBertato, Linda, Nicola Chirico, and Ester Papa. "QSAR Models for the Prediction of Dietary Biomagnification Factor in Fish." Toxics 11, no. 3 (February 23, 2023): 209. http://dx.doi.org/10.3390/toxics11030209.
Повний текст джерелаZhang, Jiaming, Qinqin Liu, Haoxia Zhao, Guiyu Li, Yunpeng Yi, and Ruofeng Shang. "Design and Synthesis of Pleuromutilin Derivatives as Antibacterial Agents Using Quantitative Structure–Activity Relationship Model." International Journal of Molecular Sciences 25, no. 4 (February 13, 2024): 2256. http://dx.doi.org/10.3390/ijms25042256.
Повний текст джерелаGupta, Ashish, Virender Kumar, and Polamarasetty Aparoy. "Role of Topological, Electronic, Geometrical, Constitutional and Quantum Chemical Based Descriptors in QSAR: mPGES-1 as a Case Study." Current Topics in Medicinal Chemistry 18, no. 13 (October 4, 2018): 1075–90. http://dx.doi.org/10.2174/1568026618666180719164149.
Повний текст джерелаRahmouni, Ali, Moufida Touhami, and Tahar Benaissa. "Fukui Indices as QSAR Model Descriptors." International Journal of Chemoinformatics and Chemical Engineering 6, no. 2 (July 2017): 31–44. http://dx.doi.org/10.4018/ijcce.2017070103.
Повний текст джерелаDiyah, Nuzul Wahyuning, Dhea Ananda Ainurrizma, and Denayu Pebrianti. "Design of acyl salicylic acid derivates as COX-1 inhibitors using QSAR approach, molecular docking and QSPR analysis." Pharmacy Education 24, no. 3 (May 1, 2024): 88–94. http://dx.doi.org/10.46542/pe.2024.243.8894.
Повний текст джерелаHelda Wika Amini, Istiqomah Rahmawati, Rizki Fitria Darmayanti, and Boy Arief Fachri. "QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP STUDY OF ESTER-BASED FERULIC ACID DERIVATIVES AGAINST CERVICAL CANCER CELL (HELA)." Journal of Biobased Chemicals 1, no. 1 (June 5, 2020): 29–37. http://dx.doi.org/10.19184/jobc.v1i1.109.
Повний текст джерелаRakhimbekova, Assima, Timur I. Madzhidov, Ramil I. Nugmanov, Timur R. Gimadiev, Igor I. Baskin, and Alexandre Varnek. "Comprehensive Analysis of Applicability Domains of QSPR Models for Chemical Reactions." International Journal of Molecular Sciences 21, no. 15 (August 3, 2020): 5542. http://dx.doi.org/10.3390/ijms21155542.
Повний текст джерелаZaki, Magdi E. A., Sami A. Al-Hussain, Vijay H. Masand, Siddhartha Akasapu, Sumit O. Bajaj, Nahed N. E. El-Sayed, Arabinda Ghosh, and Israa Lewaa. "Identification of Anti-SARS-CoV-2 Compounds from Food Using QSAR-Based Virtual Screening, Molecular Docking, and Molecular Dynamics Simulation Analysis." Pharmaceuticals 14, no. 4 (April 13, 2021): 357. http://dx.doi.org/10.3390/ph14040357.
Повний текст джерелаXu, Yong-jin, and Hua Gao. "Dimension related distance and its application in QSAR/QSPR model error estimation." QSAR & Combinatorial Science 22, no. 4 (May 2003): 422–29. http://dx.doi.org/10.1002/qsar.200390032.
Повний текст джерелаSharma, M. C., and D. V. Kohli. "DEVELOPMENT OF A ROBUST QSAR MODEL OF ANGIOTENSIN RECEPTOR REVEALS A K NEAREST NEIGHBOR APPLICABLE TO DIVERSE SCAFFOLDS." INDIAN DRUGS 54, no. 06 (June 28, 2017): 30–36. http://dx.doi.org/10.53879/id.54.06.10947.
Повний текст джерелаSharma, M. C. "A QSAR STUDY OF SUBSTITUTED PYRAZOLINE DERIVATIVES AS POTENTIAL ANTI-TUBERCULOSIS AGENTS." INDIAN DRUGS 54, no. 04 (April 28, 2017): 22–31. http://dx.doi.org/10.53879/id.54.04.10781.
Повний текст джерелаMatusevičiūtė, Ramona, Eglė Ignatavičiūtė, Rokas Mickus, Sergio Bordel, Vytenis Arvydas Skeberdis, and Vytautas Raškevičius. "Evaluation of Cx43 Gap Junction Inhibitors Using a Quantitative Structure-Activity Relationship Model." Biomedicines 11, no. 7 (July 12, 2023): 1972. http://dx.doi.org/10.3390/biomedicines11071972.
Повний текст джерелаMishra, Durgesh Kumar, Ashutosh Singh, Sunil Mishra, Priti Singh, and Abhishek Singh. "PM3 Method based QSAR Study of the Derivatives of Thiadiazole and Quinoxaline for Antiepileptic Activity using Topological Descriptors." Asian Journal of Organic & Medicinal Chemistry 7, no. 1 (2022): 99–110. http://dx.doi.org/10.14233/ajomc.2022.ajomc-p370.
Повний текст джерелаChakraborty, Tanmoy, and Dulal C. Ghosh. "Correlation of the Drug Activities of Some Anti-Tubercular Chalcone Derivatives in Terms of the Quantum Mechanical Reactivity Descriptors." International Journal of Chemoinformatics and Chemical Engineering 1, no. 2 (July 2011): 53–65. http://dx.doi.org/10.4018/ijcce.2011070104.
Повний текст джерелаNaik, Pradeep Kumar, Afroz Alam, Ashutosh Malhotra, and Owasis Rizvi. "Molecular Modeling and Structure-Activity Relationship of Podophyllotoxin and Its Congeners." Journal of Biomolecular Screening 15, no. 5 (May 10, 2010): 528–40. http://dx.doi.org/10.1177/1087057110368994.
Повний текст джерелаMishra, Puja, Sumit Nandi, Ankit Chatterjee, Tridib Nayek, Souvik Basak, Kumar Halder, and Arup Mukherjee. "Development of 2D and 3D QSAR models of pyrazole derivatives as acetylcholine esterase inhibitors." Journal of the Serbian Chemical Society, no. 00 (2024): 39. http://dx.doi.org/10.2298/jsc230221039m.
Повний текст джерелаAsgaonkar, K. D., S. M. Patil, T. S. Chitre, S. D. Wani, and M. T. Singh. "QSAR tool for optimization of nitrobenzamide pharmacophore for antitubercular activity." Bulletin of the Karaganda University. "Chemistry" series 105, no. 1 (March 30, 2022): 60–68. http://dx.doi.org/10.31489/2022ch1/60-68.
Повний текст джерелаEdache, Emmanuel Israel, Adamu Uzairu, Paul Andrew Mamza, and Gideon Adamu Shallangwa. "A comparative QSAR analysis, 3D-QSAR, molecular docking and molecular design of iminoguanidine-based inhibitors of HemO: A rational approach to antibacterial drug design." Journal of Drugs and Pharmaceutical Science 4, no. 3 (August 30, 2020): 21–36. http://dx.doi.org/10.31248/jdps2020.036.
Повний текст джерелаSharma, M. C. "QSAR APPROACH TO THE STUDY OF THE EGFR TYROSINE KINASE INHIBITORS: THIAZOLYL-PYRAZOLINE DERIVATIVES." INDIAN DRUGS 54, no. 03 (March 28, 2017): 5–12. http://dx.doi.org/10.53879/id.54.03.10739.
Повний текст джерелаRaza, Zahid. "Leap Zagreb Connection Numbers for Some Networks Models." Indonesian Journal of Chemistry 20, no. 6 (July 16, 2020): 1407. http://dx.doi.org/10.22146/ijc.53393.
Повний текст джерелаZavršnik, Davorka, Samija Muratović, and Selma Špirtović. "QSAR and QSPR study of derivatives 4-arylaminocoumarin." Bosnian Journal of Basic Medical Sciences 3, no. 3 (August 20, 2003): 59–63. http://dx.doi.org/10.17305/bjbms.2003.3531.
Повний текст джерелаFaramarzi, Zohreh, Fatemeh Abbasitabar, Jalali Jahromi, and Maziar Noei. "New structure-based models for the prediction of normal boiling point temperature of ternary azeotropes." Journal of the Serbian Chemical Society 86, no. 7-8 (2021): 685–98. http://dx.doi.org/10.2298/jsc210218035f.
Повний текст джерелаDidziapetris, Remigijus, Kiril Lanevskij, and Pranas Japertas. "Trainable QSAR model of Ames genotoxicity." Toxicology Letters 180 (October 2008): S152—S153. http://dx.doi.org/10.1016/j.toxlet.2008.06.335.
Повний текст джерелаNirmalakhandan, Nagamany N., and Richard E. Speece. "QSAR model for predicting Henry's constant." Environmental Science & Technology 22, no. 11 (November 1988): 1349–57. http://dx.doi.org/10.1021/es00176a016.
Повний текст джерелаAmin, Sk Abdul, Nilanjan Adhikari, Tarun Jha, and Shovanlal Gayen. "Exploring structural requirements of unconventional Knoevenagel-type indole derivatives as anticancer agents through comparative QSAR modeling approaches." Canadian Journal of Chemistry 94, no. 7 (July 2016): 637–44. http://dx.doi.org/10.1139/cjc-2016-0050.
Повний текст джерелаPandit, Bibhas, Yogesh Vaishnav, Sanjib Bahadur, and Trilochan Satapathy. "2D & 3D-QSAR Studies on a Series of Quinoline-Amino-piperidine Derivatives as Potent Mycobacterium DNA-Gyrase-B Inhibitors." International Journal of Pharmaceutical Sciences and Nanotechnology(IJPSN) 16, no. 3 (May 31, 2023): 6512–21. http://dx.doi.org/10.37285/ijpsn.2023.16.3.5.
Повний текст джерелаEmdeniz. "PENGGUNAAN FRONTIER ORBITAL MOLEKUL SEBAGAI DESKRIPTOR PADA ANALISIS HUBUNGAN KUANTITATIF STRUKTUR AKTIVITAS (HKSA) TOKSIK SENYAWA KHLOROFENOL." Jurnal Riset Kimia 5, no. 2 (March 15, 2012): 116. http://dx.doi.org/10.25077/jrk.v5i2.211.
Повний текст джерелаTerzioglu, Nalan, and Hans-Dieter Höltje. "Receptor-Based 3D QSAR Analysis of Serotonin 5-HT1D Receptor Agonists." Collection of Czechoslovak Chemical Communications 70, no. 9 (2005): 1482–92. http://dx.doi.org/10.1135/cccc20051482.
Повний текст джерелаNasution, Hasmalina, Nur Enizan, Nurlaili Nurlaili, and Jufrizal Syahri. "Design of Trolox Compounds as Antioxidant and Their Analysis Using Quantitative Structure Activity Relationship." Acta Chimica Asiana 3, no. 2 (October 18, 2020): 181. http://dx.doi.org/10.29303/aca.v3i2.40.
Повний текст джерела