Oishi S - Search Results

1

CXCL12/CXCR4 pathway is activated by oncogenic JAK2 in a PI3K-dependent manner.

Abdelouahab H, Zhang Y, Wittner M, Oishi S, Fujii N, Besancenot R, Plo I, Ribrag V, Solary E, Vainchenker W, Barosi G, Louache F. Abdelouahab H, et al. Among authors: oishi s. Oncotarget. 2016 Jul 22;8(33):54082-54095. doi: 10.18632/oncotarget.10789. eCollection 2017 Aug 15. Oncotarget. 2016. PMID: 28903325 Free PMC article.

2

Synthesis of allenes from allylic alcohol derivatives bearing a bromine atom using a palladium(0)/diethylzinc system.

Ohno H, Miyamura K, Tanaka T, Oishi S, Toda A, Takemoto Y, Fujii N, Ibuka T. Ohno H, et al. Among authors: oishi s. J Org Chem. 2002 Feb 22;67(4):1359-67. doi: 10.1021/jo016320y. J Org Chem. 2002. PMID: 11846687

3

Diastereoselective synthesis of psi[(E)-CH=CMe]- and psi[(Z)-CH=CMe]-type dipeptide isosteres by organocopper-mediated anti-S(N)2' reaction.

Oishi S, Kamano T, Niida A, Odagaki Y, Tamamura H, Otaka A, Hamanaka N, Fujii N. Oishi S, et al. Org Lett. 2002 Apr 4;4(7):1051-4. doi: 10.1021/ol016834j. Org Lett. 2002. PMID: 11922780

4

Diastereoselective synthesis of psi[(E)-CMe=CH]- and psi[(E)-CMe=CMe]- type dipeptide isosteres based on organocopper-mediated anti-S(N)2' reaction.

Oishi S, Niida A, Kamano T, Odagaki Y, Tamamura H, Otaka A, Hamanaka N, Fujii N. Oishi S, et al. Org Lett. 2002 Apr 4;4(7):1055-8. doi: 10.1021/ol016835b. Org Lett. 2002. PMID: 11922781

5

Regio- and stereoselective synthesis of (E)-alkene trans-Xaa-Pro dipeptide mimetics utilizing organocopper-mediated anti-S(N)2' reactions.

Otaka A, Katagiri F, Kinoshita T, Odagaki Y, Oishi S, Tamamura H, Hamanaka N, Fujii N. Otaka A, et al. Among authors: oishi s. J Org Chem. 2002 Aug 23;67(17):6152-61. doi: 10.1021/jo025922u. J Org Chem. 2002. PMID: 12182656

6

Diastereoselective synthesis of new psi[(E)-CH=CMe]- and psi[(Z)-CH=CMe]-type alkene dipeptide isosteres by organocopper reagents and application to conformationally restricted cyclic RGD peptidomimetics.

Oishi S, Kamano T, Niida A, Odagaki Y, Hamanaka N, Yamamoto M, Ajito K, Tamamura H, Otaka A, Fujii N. Oishi S, et al. J Org Chem. 2002 Aug 23;67(17):6162-73. doi: 10.1021/jo025923m. J Org Chem. 2002. PMID: 12182657

7

Molecular-size reduction of a potent CXCR4-chemokine antagonist using orthogonal combination of conformation- and sequence-based libraries.

Fujii N, Oishi S, Hiramatsu K, Araki T, Ueda S, Tamamura H, Otaka A, Kusano S, Terakubo S, Nakashima H, Broach JA, Trent JO, Wang ZX, Peiper SC. Fujii N, et al. Among authors: oishi s. Angew Chem Int Ed Engl. 2003 Jul 21;42(28):3251-3. doi: 10.1002/anie.200351024. Angew Chem Int Ed Engl. 2003. PMID: 12876735 No abstract available.

8

SmI2-mediated reduction of gamma,gamma-difluoro-alpha,beta-enoates with application to the synthesis of functionalized (Z)-fluoroalkene-type dipeptide isosteres.

Otaka A, Watanabe J, Yukimasa A, Sasaki Y, Watanabe H, Kinoshita T, Oishi S, Tamamura H, Fujii N. Otaka A, et al. Among authors: oishi s. J Org Chem. 2004 Mar 5;69(5):1634-45. doi: 10.1021/jo035709d. J Org Chem. 2004. PMID: 14987023

9

Metastin and its variant forms suppress migration of pancreatic cancer cells.

Masui T, Doi R, Mori T, Toyoda E, Koizumi M, Kami K, Ito D, Peiper SC, Broach JR, Oishi S, Niida A, Fujii N, Imamura M. Masui T, et al. Among authors: oishi s. Biochem Biophys Res Commun. 2004 Feb 27;315(1):85-92. doi: 10.1016/j.bbrc.2004.01.021. Biochem Biophys Res Commun. 2004. PMID: 15013429

10

Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activity.

Niida A, Wang Z, Tomita K, Oishi S, Tamamura H, Otaka A, Navenot JM, Broach JR, Peiper SC, Fujii N. Niida A, et al. Among authors: oishi s. Bioorg Med Chem Lett. 2006 Jan 1;16(1):134-7. doi: 10.1016/j.bmcl.2005.09.054. Epub 2005 Oct 18. Bioorg Med Chem Lett. 2006. PMID: 16242330

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