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Bioorganic & Medicinal Chemistry|August 1, 2009
Synthesis of orthogonally reactive FK506 derivatives via olefin cross metathesisPaul S Marinec, Christopher G Evans, Garrett S Gibbons, et al.Bioorganic & Medicinal Chemistry|August 4, 2009
Microbial transformation of isosteviol oxime and the inhibitory effects on NF-kappaB and AP-1 activation in LPS-stimulated macrophagesShwu-Fen Chang, Bo-Hon Chou, Li-Ming Yang, et al.Bioorganic & Medicinal Chemistry|May 12, 2009
2-(3-Aryl-2-propenoyl)-3-methylquinoxaline-1,4-dioxides: a novel cluster of tumor-specific cytotoxins which reverse multidrug resistanceUmashankar Das, Hari N Pati, Atulya K Panda, et al.Bioorganic & Medicinal Chemistry|May 12, 2009
Design and synthesis of enediyne-peptide conjugates and their inhibiting activity against chymotrypsinSansa Dutta, Amit Basak, Swagata DasguptaBioorganic & Medicinal Chemistry|May 14, 2009
Biological activity of endomorphin and [Dmt1]endomorphin analogs with six-membered proline surrogates in position 2Renata Perlikowska, Katarzyna Gach, Jakub Fichna, et al.Bioorganic & Medicinal Chemistry|May 16, 2009
Synthesis and antiviral activity evaluation of acyclic 2'-azanucleosides bearing a phosphonomethoxy function in the side chainMariola Koszytkowska-Stawińska, Erik De Clercq, Jan BalzariniBioorganic & Medicinal Chemistry|May 16, 2009
Lathyrane diterpenes from Euphorbia lathyris as modulators of multidrug resistance and their crystal structuresWei Jiao, Weiwei Dong, Zhefeng Li, et al.Bioorganic & Medicinal Chemistry|September 29, 2009
Synthesis and evaluation of novel alpha-heteroaryl-phenylpropanoic acid derivatives as PPARalpha/gamma dual agonistsAgustin Casimiro-Garcia, Christopher F Bigge, Jo Ann Davis, et al.Bioorganic & Medicinal Chemistry|September 29, 2009
Synthesis and biological evaluation of 14-(aminoalkyl-aminomethyl)aromathecins as topoisomerase I inhibitors: investigating the hypothesis of shared structure-activity relationshipsMaris A Cinelli, Brenda Cordero, Thomas S Dexheimer, et al.Bioorganic & Medicinal Chemistry|September 29, 2009
Synthesis and evaluation of non-hydrolyzable D-mannose 6-phosphate surrogates reveal 6-deoxy-6-dicarboxymethyl-D-mannose as a new strong inhibitor of phosphomannose isomerasesJohanna Foret, Benoit de Courcy, Nohad Gresh, et al.Pageof 1,701