| Year |
Citation |
Score |
| 2019 |
Zhang F, Braun DR, Rajski SR, DeMaria D, Bugni TS. Enhypyrazinones A and B, Pyrazinone Natural Products from a Marine-Derived Myxobacterium sp. Marine Drugs. 17. PMID 31842310 DOI: 10.3390/Md17120698 |
0.313 |
|
| 2011 |
Zhao LX, Huang SX, Tang SK, Jiang CL, Duan Y, Beutler JA, Henrich CJ, McMahon JB, Schmid T, Blees JS, Colburn NH, Rajski SR, Shen B. Actinopolysporins A-C and tubercidin as a Pdcd4 stabilizer from the halophilic actinomycete Actinopolyspora erythraea YIM 90600. Journal of Natural Products. 74: 1990-5. PMID 21870828 DOI: 10.1021/Np200603G |
0.31 |
|
| 2011 |
Smanski MJ, Yu Z, Casper J, Lin S, Peterson RM, Chen Y, Wendt-Pienkowski E, Rajski SR, Shen B. Dedicated ent-kaurene and ent-atiserene synthases for platensimycin and platencin biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 108: 13498-503. PMID 21825154 DOI: 10.1073/Pnas.1106919108 |
0.323 |
|
| 2010 |
Chen Y, Wendt-Pienkowski E, Ju J, Lin S, Rajski SR, Shen B. Characterization of FdmV as an amide synthetase for fredericamycin A biosynthesis in Streptomyces griseus ATCC 43944. The Journal of Biological Chemistry. 285: 38853-60. PMID 20926388 DOI: 10.1074/Jbc.M110.147744 |
0.321 |
|
| 2010 |
Huang SX, Powell E, Rajski SR, Zhao LX, Jiang CL, Duan Y, Xu W, Shen B. Discovery and total synthesis of a new estrogen receptor heterodimerizing actinopolymorphol A from Actinopolymorpha rutilus. Organic Letters. 12: 3525-7. PMID 20593804 DOI: 10.1021/Ol1013526 |
0.34 |
|
| 2010 |
Luo Y, Li W, Ju J, Yuan Q, Peters NR, Hoffmann FM, Huang SX, Bugni TS, Rajski S, Osada H, Shen B. Functional characterization of TtnD and TtnF, unveiling new insights into tautomycetin biosynthesis. Journal of the American Chemical Society. 132: 6663-71. PMID 20426415 DOI: 10.1021/Ja9082446 |
0.33 |
|
| 2009 |
Chen Y, Wendt-Pienkoski E, Rajski SR, Shen B. In vivo investigation of the roles of FdmM and FdmM1 in fredericamycin biosynthesis unveiling a new family of oxygenases. The Journal of Biological Chemistry. 284: 24735-43. PMID 19620242 DOI: 10.1074/Jbc.M109.014191 |
0.301 |
|
| 2009 |
Ju J, Li W, Yuan Q, Peters NR, Hoffmann FM, Rajski SR, Osada H, Shen B. Functional characterization of ttmM unveils new tautomycin analogs and insight into tautomycin biosynthesis and activity. Organic Letters. 11: 1639-42. PMID 19281218 DOI: 10.1021/Ol900293J |
0.307 |
|
| 2009 |
Li W, Luo Y, Ju J, Rajski SR, Osada H, Shen B. Characterization of the tautomycetin biosynthetic gene cluster from Streptomyces griseochromogenes provides new insight into dialkylmaleic anhydride biosynthesis. Journal of Natural Products. 72: 450-9. PMID 19191560 DOI: 10.1021/Np8007478 |
0.326 |
|
| 2008 |
Li W, Ju J, Rajski SR, Osada H, Shen B. Characterization of the tautomycin biosynthetic gene cluster from Streptomyces spiroverticillatus unveiling new insights into dialkylmaleic anhydride and polyketide biosynthesis. The Journal of Biological Chemistry. 283: 28607-17. PMID 18708355 DOI: 10.1074/Jbc.M804279200 |
0.324 |
|
| 2008 |
Osborne T, Roska RL, Rajski SR, Thompson PR. In situ generation of a bisubstrate analogue for protein arginine methyltransferase 1. Journal of the American Chemical Society. 130: 4574-5. PMID 18338885 DOI: 10.1021/Ja077104V |
0.367 |
|
| 2008 |
Mays JR, Weller Roska RL, Sarfaraz S, Mukhtar H, Rajski SR. Identification, synthesis, and enzymology of non-natural glucosinolate chemopreventive candidates. Chembiochem : a European Journal of Chemical Biology. 9: 729-47. PMID 18327862 DOI: 10.1002/Cbic.200700586 |
0.762 |
|
| 2008 |
Chen Y, Luo Y, Ju J, Wendt-Pienkowski E, Rajski SR, Shen B. Identification of fredericamycin E from Streptomyces griseus: Insights into fredericamycin A biosynthesis highlighting carbaspirocycle formation. Journal of Natural Products. 71: 431-7. PMID 18232659 DOI: 10.1021/Np070664N |
0.369 |
|
| 2007 |
Mays JR, Restituyo JA, Katzenberger RJ, Wassarman DA, Rajski SR. Cyclic Disulfides as Functional Mimics of the Histone Deacetylase Inhibitor FK-228. Tetrahedron Letters. 48: 4579-4583. PMID 18575573 DOI: 10.1016/J.Tetlet.2007.04.123 |
0.68 |
|
| 2006 |
Zhang C, Weller RL, Thorson JS, Rajski SR. Natural product diversification using a non-natural cofactor analogue of S-adenosyl-L-methionine. Journal of the American Chemical Society. 128: 2760-1. PMID 16506729 DOI: 10.1021/Ja056231T |
0.779 |
|
| 2006 |
Weller RL, Rajski SR. Design, synthesis, and preliminary biological evaluation of a DNA methyltransferase-directed alkylating agent. Chembiochem : a European Journal of Chemical Biology. 7: 243-5. PMID 16365907 DOI: 10.1002/Cbic.200500362 |
0.772 |
|
| 2006 |
Weller RL, Rajski SR. Cover Picture: Design, Synthesis, and Preliminary Biological Evaluation of a DNA Methyltransferase-Directed Alkylating Agent (ChemBioChem 2/2006) Chembiochem. 7: 217-217. DOI: 10.1002/Cbic.200690003 |
0.773 |
|
| 2005 |
Comstock LR, Rajski SR. Methyltransferase-directed DNA strand scission. Journal of the American Chemical Society. 127: 14136-7. PMID 16218579 DOI: 10.1021/Ja054128Y |
0.736 |
|
| 2005 |
Petersen SG, Rajski SR. o-nitrobenzenesulfonamides in nucleoside synthesis: efficient 5'-aziridination of adenosine. The Journal of Organic Chemistry. 70: 5833-9. PMID 16018675 DOI: 10.1021/Jo050205W |
0.737 |
|
| 2005 |
Weller RL, Rajski SR. DNA methyltransferase-moderated click chemistry. Organic Letters. 7: 2141-4. PMID 15901154 DOI: 10.1021/Ol0504749 |
0.775 |
|
| 2005 |
Comstock LR, Rajski SR. Conversion of DNA methyltransferases into azidonucleosidyl transferases via synthetic cofactors. Nucleic Acids Research. 33: 1644-52. PMID 15778434 DOI: 10.1093/Nar/Gki306 |
0.756 |
|
| 2004 |
Comstock LR, Rajski SR. Efficient synthesis of azide-bearing cofactor mimics. The Journal of Organic Chemistry. 69: 1425-8. PMID 14961711 DOI: 10.1021/Jo035485Z |
0.754 |
|
| 2004 |
Weller RL, Rajski SR. Aziridination of γ,δ-Dibromoethyl-2-pentenoate with Primary Amines: Extension of the Gabriel—Cromwell Reaction. Cheminform. 35. DOI: 10.1016/J.Tetlet.2004.06.005 |
0.761 |
|
| 2004 |
Weller RL, Rajski SR. Aziridination of γ,δ-dibromoethyl-2-pentenoate with primary amines: extension of the Gabriel–Cromwell reaction Tetrahedron Letters. 45: 5807-5810. DOI: 10.1016/J.TETLET.2004.06.005 |
0.745 |
|
| 2003 |
Restituyo JA, Comstock LR, Petersen SG, Stringfellow T, Rajski SR. Conversion of aryl azides to O-alkyl imidates via modified Staudinger ligation. Organic Letters. 5: 4357-60. PMID 14601999 DOI: 10.1021/Ol035635S |
0.683 |
|
| 2002 |
Comstock LR, Rajski SR. Expeditious synthesis of aziridine-based cofactor mimics Tetrahedron. 58: 6019-6026. DOI: 10.1016/S0040-4020(02)00590-2 |
0.752 |
|
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