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1

Skalkos, Dimitris, James A. Hampton, Rick W. Keck, Miriam Wagoner, and Steven H. Selman. "IMINIUM SALT BENZOCHLORINS: STRUCTURE-ACTIVITY RELATIONSHIP STUDIES." Photochemistry and Photobiology 59, no. 2 (1994): 175–81. http://dx.doi.org/10.1111/j.1751-1097.1994.tb05019.x.

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2

German, Nadezhda A., Ann M. Decker, Brian P. Gilmour, Brian F. Thomas, and Yanan Zhang. "Truncated Orexin Peptides: Structure–Activity Relationship Studies." ACS Medicinal Chemistry Letters 4, no. 12 (2013): 1224–27. http://dx.doi.org/10.1021/ml400333a.

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3

Patil, Nitin A., K. Johan Rosengren, Frances Separovic, John D. Wade, Ross A. D. Bathgate, and Mohammed Akhter Hossain. "Relaxin family peptides: structure-activity relationship studies." British Journal of Pharmacology 174, no. 10 (2017): 950–61. http://dx.doi.org/10.1111/bph.13684.

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4

Ma, Anqi, Wenyu Yu, Yan Xiong, Kyle V. Butler, Peter J. Brown, and Jian Jin. "Structure–activity relationship studies of SETD8 inhibitors." MedChemComm 5, no. 12 (2014): 1892–98. http://dx.doi.org/10.1039/c4md00317a.

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5

Ko, Horng-Huey, Lo-Ti Tsao, Kun-Lung Yu, Cheng-Tsung Liu, Jih-Pyang Wang, and Chun-Nan Lin. "Structure–activity relationship studies on chalcone derivatives." Bioorganic & Medicinal Chemistry 11, no. 1 (2003): 105–11. http://dx.doi.org/10.1016/s0968-0896(02)00312-7.

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6

Murthi, Krishna K., Marja Dubay, Christopher McClure, et al. "Structure–activity relationship studies of flavopiridol analogues." Bioorganic & Medicinal Chemistry Letters 10, no. 10 (2000): 1037–41. http://dx.doi.org/10.1016/s0960-894x(00)00156-6.

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7

Tsukano, Chihiro, and Makoto Sasaki. "Structure–activity relationship studies of gymnocin-A." Tetrahedron Letters 47, no. 38 (2006): 6803–7. http://dx.doi.org/10.1016/j.tetlet.2006.07.081.

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8

Fuchs, James R., Bulbul Pandit, Deepak Bhasin, et al. "Structure–activity relationship studies of curcumin analogues." Bioorganic & Medicinal Chemistry Letters 19, no. 7 (2009): 2065–69. http://dx.doi.org/10.1016/j.bmcl.2009.01.104.

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9

Cheuka, Peter Mubanga, Diego Gonzalez Cabrera, Tanya Paquet, and Kelly Chibale. "Structure–activity relationship studies of antiplasmodial aminomethylthiazoles." Bioorganic & Medicinal Chemistry Letters 24, no. 22 (2014): 5207–11. http://dx.doi.org/10.1016/j.bmcl.2014.09.071.

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10

Wiker, Franziska, Nils Hauck, Stephanie Grond, and Bertolt Gust. "Caprazamycins: Biosynthesis and structure activity relationship studies." International Journal of Medical Microbiology 309, no. 5 (2019): 319–24. http://dx.doi.org/10.1016/j.ijmm.2019.05.004.

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11

Klopman, G., S. Wang, M. R. Jacobs, and J. J. Ellner. "Anti-Mycobacterium avium activity of quinolones: structure-activity relationship studies." Antimicrobial Agents and Chemotherapy 37, no. 9 (1993): 1807–15. http://dx.doi.org/10.1128/aac.37.9.1807.

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12

Gupta, Satya. "Quantitative Structure-Activity Relationship Studies on Cholecystokinin Antagonists." Current Pharmaceutical Design 8, no. 2 (2002): 111–24. http://dx.doi.org/10.2174/1381612023396500.

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13

Gupta, Satya, and Anantha Nagappa. "Quantitative Structure-Activity Relationship Studies on Cholecystokin Antagonists." Medicinal Chemistry Reviews - Online 1, no. 3 (2004): 349–50. http://dx.doi.org/10.2174/1567203043401680.

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14

Neves, Ana R., Marta Correia-da-Silva, Emília Sousa, and Madalena Pinto. "Structure–activity relationship studies for multitarget antithrombotic drugs." Future Medicinal Chemistry 8, no. 18 (2016): 2305–55. http://dx.doi.org/10.4155/fmc-2015-0020.

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15

Nelson, Derek W., Kathy Sarris, Douglas M. Kalvin, et al. "Structure−Activity Relationship Studies onN′-Aryl Carbohydrazide P2X7Antagonists." Journal of Medicinal Chemistry 51, no. 10 (2008): 3030–34. http://dx.doi.org/10.1021/jm701516f.

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16

Burden, Frank R. "Quantitative Structure−Activity Relationship Studies Using Gaussian Processes." Journal of Chemical Information and Computer Sciences 41, no. 3 (2001): 830–35. http://dx.doi.org/10.1021/ci000459c.

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17

Gupta, S. P. "Quantitative Structure-Activity Relationship Studies on Anticancer Drugs." Chemical Reviews 94, no. 6 (1994): 1507–51. http://dx.doi.org/10.1021/cr00030a003.

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18

Jaeger, EP, PC Jurs, and TR Stouch. "Structure-activity relationship studies of retinoid cancer inhibition." European Journal of Medicinal Chemistry 28, no. 4 (1993): 275–90. http://dx.doi.org/10.1016/0223-5234(93)90145-5.

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19

Murugesan, Dinakaran, Marcel Kaiser, Karen L. White, et al. "Structure–Activity Relationship Studies of Pyrrolone Antimalarial Agents." ChemMedChem 8, no. 9 (2013): 1537–44. http://dx.doi.org/10.1002/cmdc.201300177.

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20

Suryanarayana, M. V. S., K. S. Pandey, Shri Prakash, et al. "Structure-Activity Relationship Studies with Mosquito Repellent Amides." Journal of Pharmaceutical Sciences 80, no. 11 (1991): 1055–57. http://dx.doi.org/10.1002/jps.2600801111.

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21

Iyamu, Iredia D., Yingzhao Zhao, Prakash T. Parvatkar, et al. "Structure-activity and structure-property relationship studies of spirocyclic chromanes with antimalarial activity." Bioorganic & Medicinal Chemistry 57 (March 2022): 116629. http://dx.doi.org/10.1016/j.bmc.2022.116629.

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22

Tsai, C. C., P. J. Durand, K. J. McCabe, and J. W. Baker. "Structure-activity relationship studies of nucleoside analogs with anti-HIV activity." Antiviral Research 30, no. 1 (1996): A29. http://dx.doi.org/10.1016/0166-3542(96)80263-4.

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23

Rajwade, R. P. "Quantitative structure–activity relationship (QSAR) studies on antitumor activity: glutamine analogues." New Biotechnology 27 (April 2010): S22—S23. http://dx.doi.org/10.1016/j.nbt.2010.01.015.

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24

Galas, M. C., M. F. Lignon, M. Rodriguez, et al. "Structure-activity relationship studies on cholecystokinin: analogues with partial agonist activity." American Journal of Physiology-Gastrointestinal and Liver Physiology 254, no. 2 (1988): G176—G182. http://dx.doi.org/10.1152/ajpgi.1988.254.2.g176.

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In the present study, hepta- and octapeptide analogues of the C-terminal part of cholecystokinin, modified on the C-terminal phenylalanine residue, were synthesized. CCK analogues were prepared in which the peptide bond between aspartic acid and phenylalanine had or had not been modified and were lacking the C-terminal primary amide function. These CCK derivatives were able to cause full stimulation of amylase release from rat pancreatic acini but without a decrease in amylase release at supramaximal concentrations. There was a close relationship between the abilities of these derivatives to s
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25

Subramanian, Santhosh, Nam-Soo Kim, Pillaiyar Thanigaimalai, et al. "Structure–activity relationship studies of novel arylsulfonylimidazolidinones for their anticancer activity." European Journal of Medicinal Chemistry 46, no. 8 (2011): 3258–64. http://dx.doi.org/10.1016/j.ejmech.2011.04.042.

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26

Chang-Ying, Chen, Ding Xiao-Qin, and Feng Shan. "Studies on Electronic Structure and Structure-Activity Relationship of Ciguatoxin(CTX)." Acta Physico-Chimica Sinica 16, no. 04 (2000): 307–11. http://dx.doi.org/10.3866/pku.whxb20000404.

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27

Lu, X., D. Lu, M. Scully, and V. Kakkar. "Structure-Activity Relationship Studies on ADAM Protein-Integrin Interactions." Cardiovascular & Hematological Agents in Medicinal Chemistry 5, no. 1 (2007): 29–42. http://dx.doi.org/10.2174/187152507779315822.

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28

Boyle, Craig, and Anandan Palani. "Structure-Activity Relationship Studies: M2 and CCR5 Receptor Antagonists." Current Topics in Medicinal Chemistry 3, no. 10 (2003): 1155–69. http://dx.doi.org/10.2174/1568026033452032.

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29

Milojković-Opsenica, Dušanka, Filip Andrić, Sandra Šegan, Jelena Trifković, and Živoslav Tešić. "Thin-layer chromatography in quantitative structure-activity relationship studies." Journal of Liquid Chromatography & Related Technologies 41, no. 6 (2018): 272–81. http://dx.doi.org/10.1080/10826076.2018.1447892.

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30

Bernardo, Paul H., Kah-Fei Wan, Thirunavukkarasu Sivaraman, et al. "Structure−Activity Relationship Studies of Phenanthridine-Based Bcl-XLInhibitors." Journal of Medicinal Chemistry 51, no. 21 (2008): 6699–710. http://dx.doi.org/10.1021/jm8005433.

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31

Liu, Xiaofan, Yanping Wang, Richard I. Duclos, and George A. O’Doherty. "Stereochemical Structure Activity Relationship Studies (S-SAR) of Tetrahydrolipstatin." ACS Medicinal Chemistry Letters 9, no. 3 (2018): 274–78. http://dx.doi.org/10.1021/acsmedchemlett.8b00050.

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32

Knight, Jennifer L., та Charles L. Brooks. "Multisite λ Dynamics for Simulated Structure–Activity Relationship Studies". Journal of Chemical Theory and Computation 7, № 9 (2011): 2728–39. http://dx.doi.org/10.1021/ct200444f.

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33

Liu, S. P., Q. C. Huang, Y. Q. Tang, and Z. W. Qi. "Studies of the structure-activity relationship of TTI inhibitor." Acta Crystallographica Section A Foundations of Crystallography 49, s1 (1993): c153. http://dx.doi.org/10.1107/s010876737809563x.

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34

Wu, Chunlei, Zhengyin Pan, Guiyang Yao, Wei Wang, Lijing Fang, and Wu Su. "Synthesis and structure–activity relationship studies of teixobactin analogues." RSC Advances 7, no. 4 (2017): 1923–26. http://dx.doi.org/10.1039/c6ra26567g.

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35

Ozkan, Refik, and Nurten Tezer. "Structure–activity relationship studies on aza analogues of illudins." Journal of Molecular Structure: THEOCHEM 572, no. 1-3 (2001): 15–24. http://dx.doi.org/10.1016/s0166-1280(01)00574-7.

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36

Braga, R. S., R. Vendrame та D. S. Galvão. "Structure−Activity Relationship Studies of Substituted 17α-Acetoxyprogesterone Hormones". Journal of Chemical Information and Computer Sciences 40, № 6 (2000): 1377–85. http://dx.doi.org/10.1021/ci000454f.

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37

Gupta, S. P. "QSAR (quantitative structure-activity relationship) studies on local anesthetics." Chemical Reviews 91, no. 6 (1991): 1109–19. http://dx.doi.org/10.1021/cr00006a001.

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38

Cheon, Seung Hoon, Joon Suck Park, Joon Yeol Lee, et al. "Structure-activity relationship studies of isoquinolinone type anticancer agent." Archives of Pharmacal Research 24, no. 4 (2001): 276–80. http://dx.doi.org/10.1007/bf02975091.

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39

Misra, Milind, Qing Shi, Xiaocong Ye, et al. "Quantitative structure–activity relationship studies of threo-methylphenidate analogs." Bioorganic & Medicinal Chemistry 18, no. 20 (2010): 7221–38. http://dx.doi.org/10.1016/j.bmc.2010.08.034.

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40

Hermkens, Pedro H. H., Harry C. J. Ottenheijm, Jane M. L. van der Werf-Pieters, Chris L. E. Broekkamp, Thijs de Boer, and Jan W. van Nispen. "CCK-A Agonists: Endeavours involving structure-activity relationship studies." Recueil des Travaux Chimiques des Pays-Bas 112, no. 2 (2010): 95–106. http://dx.doi.org/10.1002/recl.19931120205.

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41

Murthi, Krishna K., Marja Dubay, Christopher McClure, et al. "ChemInform Abstract: Structure-Activity Relationship Studies of Flavopiridol Analogues." ChemInform 31, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.200035118.

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42

Xue, Chao-Bin, Wan-Chun Luo, Qi Ding, Shou-Zhu Liu, and Xing-Xiang Gao. "Quantitative structure–activity relationship studies of mushroom tyrosinase inhibitors." Journal of Computer-Aided Molecular Design 22, no. 5 (2008): 299–309. http://dx.doi.org/10.1007/s10822-008-9187-6.

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43

Xu, Lu, Jia-An Yang, and Ya-Ping Wu. "Effective Descriptions of Molecular Structures and the Quantitative Structure−Activity Relationship Studies." Journal of Chemical Information and Computer Sciences 42, no. 3 (2002): 602–6. http://dx.doi.org/10.1021/ci010092r.

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44

Guerrero, Ligia, Julián Castillo, Mar Quiñones, et al. "Inhibition of Angiotensin-Converting Enzyme Activity by Flavonoids: Structure-Activity Relationship Studies." PLoS ONE 7, no. 11 (2012): e49493. http://dx.doi.org/10.1371/journal.pone.0049493.

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45

Akester, Jessica N., Paul Njaria, Aloysius Nchinda, et al. "Synthesis, Structure–Activity Relationship, and Mechanistic Studies of Aminoquinazolinones Displaying Antimycobacterial Activity." ACS Infectious Diseases 6, no. 7 (2020): 1951–64. http://dx.doi.org/10.1021/acsinfecdis.0c00252.

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46

Indra, Bachtiar, Kimihiro Matsunaga, Osamu Hoshino, Masaji Suzuki, Hiromichi Ogasawara та Yasushi Ohizumi. "Structure–activity relationship studies with (±)-nantenine derivatives for α1-adrenoceptor antagonist activity". European Journal of Pharmacology 437, № 3 (2002): 173–78. http://dx.doi.org/10.1016/s0014-2999(02)01303-1.

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47

Moreira, Joana, Lucilia Saraiva, Madalena M. Pinto, and Honorina Cidade. "Diarylpentanoids with antitumor activity: A critical review of structure-activity relationship studies." European Journal of Medicinal Chemistry 192 (April 2020): 112177. http://dx.doi.org/10.1016/j.ejmech.2020.112177.

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48

Wang, Peng, Lin-Feng Li, Qing-Yin Wang, Lu-Qing Shang, Pei-Yong Shi, and Zheng Yin. "Anti-Dengue-Virus Activity and Structure-Activity Relationship Studies of Lycorine Derivatives." ChemMedChem 9, no. 7 (2014): 1522–33. http://dx.doi.org/10.1002/cmdc.201300505.

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49

Du, Juan, Lili Xi, Beilei Lei, et al. "Structure-based quantitative structure-activity relationship studies of checkpoint kinase 1 inhibitors." Journal of Computational Chemistry 31, no. 15 (2010): 2783–93. http://dx.doi.org/10.1002/jcc.21571.

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50

Javor, Sacha, and Jean-Louis Reymond. "Structure-Activity Relationship Studies in Single-Site Esterase Peptide Dendrimers." Israel Journal of Chemistry 49, no. 1 (2009): 129–36. http://dx.doi.org/10.1560/ijc.49.1.129.

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