Crystallography Open Database
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Result: there are 8 entries in the selection
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Searching journal of publication like 'Journal of medicinal chemistry' volume of publication is 54
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1501660 | CIF | C26 H26 N2 O2 | P 21 21 21 | 11.2339; 11.6808; 16.4783 90; 90; 90 | 2162.3 | Trapella, Claudio; Pela, Michela; Del Zoppo, Luisa; Calo, Girolamo; Camarda, Valeria; Ruzza, Chiara; Cavazzini, Alberto; Costa, Valentina; Bertolasi, Valerio; Reinscheid, Rainer K.; Salvadori, Severo; Guerrini, Remo Synthesis and separation of the enantiomers of the neuropeptide S receptor antagonist (9R/S)-3-oxo-1,1-diphenyl-tetrahydro-oxazolo[3,4-a]pyrazine-7-carboxylic acid 4-fluoro-benzylamide (SHA 68). Journal of medicinal chemistry, 2011, 54, 2738-2744 |
1501661 | CIF | C46 H36 Br4 N2 O7 | P 21 21 21 | 8.6598; 21.3183; 23.6397 90; 90; 90 | 4364.2 | Magedov, Igor V.; Frolova, Liliya; Manpadi, Madhuri; Bhoga, Uma devi; Tang, Hong; Evdokimov, Nikolai M.; George, Olivia; Georgiou, Kathy Hadje; Renner, Steffen; Getlik, Matthäus; Kinnibrugh, Tiffany L.; Fernandes, Manuel A.; Van slambrouck, Severine; Steelant, Wim F. A.; Shuster, Charles B.; Rogelj, Snezna; van Otterlo, Willem A. L.; Kornienko, Alexander Anticancer properties of an important drug lead podophyllotoxin can be efficiently mimicked by diverse heterocyclic scaffolds accessible via one-step synthesis. Journal of medicinal chemistry, 2011, 54, 4234-4246 |
1501662 | CIF | C18 H18 N4 O4 S | P 1 21/n 1 | 13.6739; 17.3161; 14.9225 90; 98.051; 90 | 3498.5 | Hall, Matthew D.; Brimacombe, Kyle R.; Varonka, Matthew S.; Pluchino, Kristen M.; Monda, Julie K.; Li, Jiayang; Walsh, Martin J.; Boxer, Matthew B.; Warren, Timothy H.; Fales, Henry M.; Gottesman, Michael M. Synthesis and structure-activity evaluation of isatin-β-thiosemicarbazones with improved selective activity toward multidrug-resistant cells expressing P-glycoprotein. Journal of medicinal chemistry, 2011, 54, 5878-5889 |
1501663 | CIF | C16 H14 N4 O S | P 1 21/c 1 | 16.7856; 5.4114; 16.1237 90; 100.73; 90 | 1438.97 | Hall, Matthew D.; Brimacombe, Kyle R.; Varonka, Matthew S.; Pluchino, Kristen M.; Monda, Julie K.; Li, Jiayang; Walsh, Martin J.; Boxer, Matthew B.; Warren, Timothy H.; Fales, Henry M.; Gottesman, Michael M. Synthesis and structure-activity evaluation of isatin-β-thiosemicarbazones with improved selective activity toward multidrug-resistant cells expressing P-glycoprotein. Journal of medicinal chemistry, 2011, 54, 5878-5889 |
1501664 | CIF | C17 H24 Br N O4 Si | P 21 21 21 | 6.5913; 15.0012; 20.319 90; 90; 90 | 2009.1 | Xin, Qisheng; Fan, Houxing; Guo, Bin; He, Huili; Gao, Suo; Wang, Hui; Huang, Yanqin; Yang, Yushe Design, synthesis, and structure-activity relationship studies of highly potent novel benzoxazinyl-oxazolidinone antibacterial agents. Journal of medicinal chemistry, 2011, 54, 7493-7502 |
1501665 | CIF | C18 H17 Cl2 F N4 O | P 1 21/c 1 | 8.1141; 10.4273; 22.6565 90; 108.576; 90 | 1817.1 | Yu, Wenquan; Goddard, Cally; Clearfield, Elizabeth; Mills, Courtney; Xiao, Tong; Guo, Haitao; Morrey, John D.; Motter, Neil E.; Zhao, Kang; Block, Timothy M.; Cuconati, Andrea; Xu, Xiaodong Design, synthesis, and biological evaluation of triazolo-pyrimidine derivatives as novel inhibitors of hepatitis B virus surface antigen (HBsAg) secretion. Journal of medicinal chemistry, 2011, 54, 5660-5670 |
1501666 | CIF | C21 H30 F3 N O3 | P 21 21 21 | 8.1766; 10.4313; 23.7612 90; 90; 90 | 2026.65 | Woods, James R.; Mo, Huaping; Bieberich, Andrew A.; Alavanja, Tanja; Colby, David A. Fluorinated amino-derivatives of the sesquiterpene lactone, parthenolide, as (19)f NMR probes in deuterium-free environments. Journal of medicinal chemistry, 2011, 54, 7934-7941 |
1501667 | CIF | C24 H21 Cl N4 O6 | P -1 | 9.0566; 12.7489; 12.9111 110.172; 103.14; 105.713 | 1259.3 | Bollini, Mariela; Domaoal, Robert A.; Thakur, Vinay V.; Gallardo-Macias, Ricardo; Spasov, Krasimir A.; Anderson, Karen S.; Jorgensen, William L. Computationally-guided optimization of a docking hit to yield catechol diethers as potent anti-HIV agents. Journal of medicinal chemistry, 2011, 54, 8582-8591 |
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