High-precision realization for sensing charged particles based on optomechanically induced two-color second-order sidebands von Wang, Junfeng, Xue, Yafeng, Liu, Shaopeng, Li, Ying, Liu, Bo

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Successful generation of structural information for fragment-based drug discovery von Öster, Linda, Tapani, Sofia, Xue, Yafeng, Käck, Helena

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Discovery of benzothiazole guanidines as novel inhibitors of thrombin and trypsin IV von Karle, Michael, Knecht, Wolfgang, Xue, Yafeng

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Discovery of Checkpoint Kinase Inhibitor (S)-5-(3-Fluorophenyl)-N-(piperidin-3-yl)-3-ureidothiophene-2-carboxamide (AZD7762) by Structure-Based Design and Optimization of Thiophene... von Oza, Vibha, Ashwell, Susan, Almeida, Lynsie, Brassil, Patrick, Breed, Jason, Deng, Chun, Gero, Thomas, Grondine, Michael, Horn, Candice, Ioannidis, Stephanos, Liu, Dongfang, Lyne, Paul, Newcombe, Nicholas, Pass, Martin, Read, Jon, Ready, Shannon, Rowsell, Siân, Su, Mei, Toader, Dorin, Vasbinder, Melissa, Yu, Dingwei, Yu, Yan, Xue, Yafeng, Zabludoff, Sonya, Janetka, James

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Total Synthesis and Structural Confirmation of Chlorodysinosin A von Hanessian, Stephen, Del Valle, Juan R, Xue, Yafeng, Blomberg, Niklas

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Structural Insights and Biological Effects of Glycogen Synthase Kinase 3-specific Inhibitor AR-A014418 von Bhat, Ratan, Xue, Yafeng, Berg, Stefan, Hellberg, Sven, Ormö, Mats, Nilsson, Yvonne, Radesäter, Ann-Cathrin, Jerning, Eva, Markgren, Per-Olof, Borgegård, Thomas, Nylöf, Martin, Giménez-Cassina, Alfredo, Hernández, Félix, Lucas, Jose J., Díaz-Nido, Javier, Avila, Jesús

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Synthesis and structure-activity relationship of 4-(1,3-benzothiazol-2-yl)-thiophene-2-sulfonamides as cyclin-dependent kinase 5 (cdk5)/p25 inhibitors von Malmström, Jonas, Viklund, Jenny, Slivo, Can, Costa, Ana, Maudet, Mickaël, Sandelin, Catrin, Hiller, Gösta, Olsson, Lise-Lotte, Aagaard, Anna, Geschwindner, Stefan, Xue, Yafeng, Vasänge, Mervi

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Exploitation of structural and regulatory diversity in glutamate racemases von Kern, Gunther, Fisher, Stewart L, de Jonge, Boudewijn L. M, Newton, D. Trevor, Lundqvist, Tomas, Xue, Yafeng, Alm, Richard A, Folmer, Rutger H. A, Keating, Thomas A

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Compounds Binding to the S2−S3 Pockets of Thrombin von Nilsson, Mikael, Hämäläinen, Markku, Ivarsson, Maria, Gottfries, Johan, Xue, Yafeng, Hansson, Sebastian, Isaksson, Roland, Fex, Tomas

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Clavatadine A, A Natural Product with Selective Recognition and Irreversible Inhibition of Factor XIa von Buchanan, Malcolm S, Carroll, Anthony R, Wessling, Deborah, Jobling, Michael, Avery, Vicky M, Davis, Rohan A, Feng, Yunjiang, Xue, Yafeng, Öster, Linda, Fex, Tomas, Deinum, Johanna, Hooper, John N. A, Quinn, Ronald J

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Experimental Study on Water Production Function for Waterlogging Stress on Corn von Kuang, Wang, Xianjiang, Yuan, Xiuqing, Cao, Yafeng, Xue

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Design and synthesis of 2′-anilino-4,4′-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3 von Swahn, Britt-Marie, Xue, Yafeng, Arzel, Erwan, Kallin, Elisabet, Magnus, Angelika, Plobeck, Niklas, Viklund, Jenny

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Discovery of the Fibrinolysis Inhibitor AZD6564, Acting via Interference of a Protein–Protein Interaction von Cheng, Leifeng, Pettersen, Daniel, Ohlsson, Bengt, Schell, Peter, Karle, Michael, Evertsson, Emma, Pahlén, Sara, Jonforsen, Maria, Plowright, Alleyn T, Boström, Jonas, Fex, Tomas, Thelin, Anders, Hilgendorf, Constanze, Xue, Yafeng, Wahlund, Göran, Lindberg, Walter, Larsson, Lars-Olof, Gustafsson, David

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Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombin von Hanessian, Stephen, Ersmark, Karolina, Wang, Xiaotian, Del Valle, Juan R., Blomberg, Niklas, Xue, Yafeng, Fjellström, Ola

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Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3 von Swahn, Britt-Marie, Huerta, Fernando, Kallin, Elisabet, Malmström, Jonas, Weigelt, Tatjana, Viklund, Jenny, Womack, Patrick, Xue, Yafeng, Öhberg, Liselotte

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Hit-to-lead studies: the discovery of potent, orally active, thiophenecarboxamide IKK-2 inhibitors von Baxter, Andrew, Brough, Steve, Cooper, Anne, Floettmann, Eike, Foster, Steve, Harding, Christine, Kettle, Jason, McInally, Tom, Martin, Craig, Mobbs, Michelle, Needham, Maurice, Newham, Pete, Paine, Stuart, St-Gallay, Steve, Salter, Sylvia, Unitt, John, Xue, Yafeng

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From natural products to achiral drug prototypes: Potent thrombin inhibitors based on P2/P3 dihydropyrid-2-one core motifs von HANESSIAN, Stephen, THERRIEN, Eric, JIANBIN ZHANG, VAN OTTERLO, Willem, YAFENG XUE, GUSTAFSSON, David, NILSSON, Ingemar, FJELLSTRÖM, Ola

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Structure-driven HtL: Design and synthesis of novel aminoindazole inhibitors of c-Jun N-terminal kinase activity von Stocks, Michael J., Barber, Simon, Ford, Rhonan, Leroux, Frederic, St-Gallay, Steve, Teague, Simon, Xue, Yafeng

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Structure-based ligand design to overcome CYP inhibition in drug discovery projects von Brändén, Gisela, Sjögren, Tove, Schnecke, Volker, Xue, Yafeng

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Fragment Screening of RORγt Using Cocktail Crystallography: Identification of Simultaneous Binding of Multiple Fragments von Xue, Yafeng, Guo, Hongwei, Hillertz, Per

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