Hayamitsu Adachi - Publications

Affiliations: 
2005-2006 Institute of Microbial Chemistry, Tokyo 

14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Adachi H, Doi H, Kasahara Y, Sawa R, Nakajima K, Kubota Y, Hosokawa N, Tateishi K, Nomoto A. Asteltoxins from the Entomopathogenic Fungus Pochonia bulbillosa 8-H-28. Journal of Natural Products. 78: 1730-4. PMID 26120875 DOI: 10.1021/Np500676J  0.316
2013 Nakae K, Kurata I, Kojima F, Igarashi M, Hatano M, Sawa R, Kubota Y, Adachi H, Nomoto A. Sacchathridine A, a prostaglandin release inhibitor from Saccharothrix sp. Journal of Natural Products. 76: 720-2. PMID 23581596 DOI: 10.1021/Np3006327  0.303
2013 Nosaka C, Adachi H, Sawa R, Nakae K, Atsumi S, Kinoshita N, Kubota Y, Igarashi M, Sei Y, Yamaguchi K, Shibuya M, Nishimura Y, Akamatsu Y. Vegfrecine, an inhibitor of VEGF receptor tyrosine kinases isolated from the culture broth of Streptomyces sp. Journal of Natural Products. 76: 715-9. PMID 23414235 DOI: 10.1021/Np300535C  0.324
2011 Hashizume H, Sawa R, Harada S, Igarashi M, Adachi H, Nishimura Y, Nomoto A. Tripropeptin C blocks the lipid cycle of cell wall biosynthesis by complex formation with undecaprenyl pyrophosphate Antimicrobial Agents and Chemotherapy. 55: 3821-3828. PMID 21628543 DOI: 10.1128/Aac.00443-11  0.312
2008 Adachi H, Kondo KI, Kojima F, Umezawa Y, Ishino K, Kunimoto H, Nishimura Y, Akamatsu Y. Structure-activity relationship study of 8-amino-2,8-dideoxy-β-KDO, a potent CMP-KDO synthetase inhibitor Letters in Drug Design and Discovery. 5: 336-339. DOI: 10.2174/157018008784912117  0.305
2007 Palaniappan KK, Gao ZG, Ivanov AA, Greaves R, Adachi H, Besada P, Kim HO, Kim AY, Choe SA, Jeong LS, Jacobson KA. Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides. Biochemistry. 46: 7437-48. PMID 17542617 DOI: 10.1021/Bi7001828  0.562
2007 Adachi H, Palaniappan KK, Ivanov AA, Bergman N, Gao ZG, Jacobson KA. Structure-activity relationships of 2,N(6),5'-substituted adenosine derivatives with potent activity at the A2B adenosine receptor. Journal of Medicinal Chemistry. 50: 1810-27. PMID 17378544 DOI: 10.1021/Jm061278Q  0.629
2006 Adachi H, Kondo K, Kojima F, Umezawa Y, Ishino K, Hotta K, Nishimura Y. Synthesis and inhibitory activity of 8-substituted 2-deoxy-beta-KDO against CMP-KDO synthetase. Natural Product Research. 20: 361-70. PMID 16644531 DOI: 10.1080/14756360500183699  0.358
2002 Adachi H, Nishimura Y, Takeuchi T. Synthesis and activities of bactobolin derivatives having new functionality at C-3. The Journal of Antibiotics. 55: 92-8. PMID 11918072 DOI: 10.7164/Antibiotics.55.92  0.316
2001 Kondo K, Adachi H, Nishimura Y, Takeuchi T. N-alkyl-3-decarboxy-3-hydroxymethylsiastatin B, a New Family of Glycosidase Inhibitors of gem-diamine 1-n-iminosugars Natural Product Letters. 15: 371-375. PMID 11838974 DOI: 10.1080/10575630108041306  0.338
2001 Kondo K, Adachi H, Shitara E, Kojima F, Nishimura Y. Glycosidase inhibitors of gem-diamine 1-N-iminosugars. structures in media of enzyme assays. Bioorganic & Medicinal Chemistry. 9: 1091-1095. PMID 11377167 DOI: 10.1016/S0968-0896(00)00330-8  0.351
2000 Nishimura Y, Shitara E, Adachi H, Toyoshima M, Nakajima M, Okami Y, Takeuchi T. Flexible synthesis and biological activity of uronic acid-type gem-diamine 1-N-iminosugars: a new family of glycosidase inhibitors. Journal of Organic Chemistry. 65: 2-11. PMID 10813888 DOI: 10.1021/Jo982448C  0.321
1998 Adachi H, Nishimura Y, Kondo S, Takeuchi T. Synthesis and activity of 3-epi-actinobolin. The Journal of Antibiotics. 51: 202-209. PMID 9544942 DOI: 10.7164/Antibiotics.51.202  0.31
1998 Adachi H, Usui T, Nishimura Y, Kondo S, Ishizuka M, Takeuchi T. Synthesis and activities of bactobolin derivatives based on the alteration of the functionality at C-3 position. The Journal of Antibiotics. 51: 184-188. PMID 9544940 DOI: 10.7164/Antibiotics.51.184  0.339
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