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Items: 1 to 20 of 70

1.

Hybrid stereoisomers of a compact molecular probe based on a jasmonic acid glucoside: syntheses and biological evaluations.

Ueda M, Yang G, Ishimaru Y, Itabashi T, Tamura S, Kiyota H, Kuwahara S, Inomata S, Shoji M, Sugai T.

Bioorg Med Chem. 2012 Oct 1;20(19):5832-43. doi: 10.1016/j.bmc.2012.08.003. Epub 2012 Aug 13.

PMID:
22963890
2.

12-hydroxyjasmonic acid glucoside is a COI1-JAZ-independent activator of leaf-closing movement in Samanea saman.

Nakamura Y, Mithöfer A, Kombrink E, Boland W, Hamamoto S, Uozumi N, Tohma K, Ueda M.

Plant Physiol. 2011 Mar;155(3):1226-36. doi: 10.1104/pp.110.168617. Epub 2011 Jan 12.

3.

Functional importance of the sugar moiety of jasmonic acid glucoside for bioactivity and target affinity.

Ueda M, Yang G, Nukadzuka Y, Ishimaru Y, Tamura S, Manabe Y.

Org Biomol Chem. 2015 Jan 7;13(1):55-8. doi: 10.1039/c4ob02106a.

PMID:
25350723
4.

Synthesis and bioactivity of potassium beta-D-glucopyranosyl 12-hydroxy jasmonate and related compounds.

Nakamura Y, Miyatake R, Inomata S, Ueda M.

Biosci Biotechnol Biochem. 2008 Nov;72(11):2867-76. Epub 2008 Nov 7.

5.

Jasmonates are phytohormones with multiple functions, including plant defense and reproduction.

Avanci NC, Luche DD, Goldman GH, Goldman MH.

Genet Mol Res. 2010 Mar 16;9(1):484-505. doi: 10.4238/vol9-1gmr754.

6.

Preparation and biological activity of molecular probes to identify and analyze jasmonic acid-binding proteins.

Jikumaru Y, Asami T, Seto H, Yoshida S, Yokoyama T, Obara N, Hasegawa M, Kodama O, Nishiyama M, Okada K, Nojiri H, Yamane H.

Biosci Biotechnol Biochem. 2004 Jul;68(7):1461-6.

7.

Potato tuber cell expansion-inducing activity of stereochemically restricted JA analogs.

Kitaoka N, Fukushi E, Koda Y, Nabeta K, Matsuura H.

Biosci Biotechnol Biochem. 2009 Aug;73(8):1872-6. Epub 2009 Aug 7.

8.

Triazoyl-phenyl linker system enhancing the aqueous solubility of a molecular probe and its efficiency in affinity labeling of a target protein for jasmonate glucoside.

Tamura S, Inomata S, Ebine M, Genji T, Iwakura I, Mukai M, Shoji M, Sugai T, Ueda M.

Bioorg Med Chem Lett. 2013 Jan 1;23(1):188-93. doi: 10.1016/j.bmcl.2012.10.124. Epub 2012 Nov 6.

PMID:
23177786
9.

Simultaneous separation of jasmonic acid conjugates with amino acids by MEKC.

Chen Y, Chen Z.

J Sep Sci. 2013 Mar;36(5):892-7. doi: 10.1002/jssc.201200934.

PMID:
23483735
10.

CYP94B3 activity against jasmonic acid amino acid conjugates and the elucidation of 12-O-β-glucopyranosyl-jasmonoyl-L-isoleucine as an additional metabolite.

Kitaoka N, Kawaide H, Amano N, Matsubara T, Nabeta K, Takahashi K, Matsuura H.

Phytochemistry. 2014 Mar;99:6-13. doi: 10.1016/j.phytochem.2013.12.019. Epub 2014 Jan 24.

PMID:
24467969
11.

Synthesis of the amino acid conjugates of epi-jasmonic acid.

Ogawa N, Kobayashi Y.

Amino Acids. 2012 May;42(5):1955-66. doi: 10.1007/s00726-011-0925-z. Epub 2011 May 12.

PMID:
21562820
12.

Iso-OPDA: an early precursor of cis-jasmone in plants?

Dabrowska P, Boland W.

Chembiochem. 2007 Dec 17;8(18):2281-5.

PMID:
18033720
13.

Design and synthesis of biotin-tagged photoaffinity probes of jasmonates.

Gu M, Yan J, Bai Z, Chen YT, Lu W, Tang J, Duan L, Xie D, Nan FJ.

Bioorg Med Chem. 2010 May 1;18(9):3012-9. doi: 10.1016/j.bmc.2010.03.059. Epub 2010 Mar 27.

PMID:
20395151
14.

Occurrence of 11-hydroxyjasmonic acid glucoside in leaflets of potato plants (Solanum tuberosum L.).

Matsuura H, Ohkubo Y, Yoshihara T.

Biosci Biotechnol Biochem. 2001 Feb;65(2):378-82.

15.
16.

Hydroxylated jasmonates are commonly occurring metabolites of jasmonic acid and contribute to a partial switch-off in jasmonate signaling.

Miersch O, Neumerkel J, Dippe M, Stenzel I, Wasternack C.

New Phytol. 2008;177(1):114-27. Epub 2007 Nov 8.

17.

Novel chemically synthesized hydroxyl-containing jasmonates as powerful inducing signals for plant secondary metabolism.

Qian ZG, Zhao ZJ, Xu Y, Qian X, Zhong JJ.

Biotechnol Bioeng. 2004 Jun 30;86(7):809-16.

PMID:
15162457
18.

Use of isotope mass probes for metabolic analysis of the jasmonate biosynthetic pathway.

Huang YQ, Liu JQ, Gong H, Yang J, Li Y, Feng YQ.

Analyst. 2011 Apr 7;136(7):1515-22. doi: 10.1039/c0an00736f. Epub 2011 Feb 18.

PMID:
21331428
19.

Cassia obtusifolia MetE as a cytosolic target for potassium isolespedezate, a leaf-opening factor of Cassia plants: target exploration by a compact molecular-probe strategy.

Ueda M, Manabe Y, Otsuka Y, Kanzawa N.

Chem Asian J. 2011 Dec 2;6(12):3286-97. doi: 10.1002/asia.201100392. Epub 2011 Aug 3.

PMID:
21815269
20.

In situ fluorescence labelling of jasmonic acid binding sites in plant tissues with cadmium-free quantum dots.

Liao Q, Yu Y, Cao Y, Lin B, Wei J.

IET Nanobiotechnol. 2015 Feb;9(1):35-42. doi: 10.1049/iet-nbt.2014.0002.

PMID:
25650324

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