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1 analyzed for the presence of alpha-AASA and pipecolic acid.
2 the alpha-allylation of tert-butoxycarbonyl pipecolic acid.
3 f FK506 has focused on esters of proline and pipecolic acid.
4 hesis of novel 2,6-cis-6-substituted-4-oxo-L-pipecolic acids.
5 mbled utilizing one-pot cyclodimerization of pipecolic acids.
6 rmationally restricted analogues of proline, pipecolic acid, 2-aminoadipic acid, or glutamic acid.
8 noid dehydroabietinal, the lysine catabolite pipecolic acid, a glycerol-3-phosphate-dependent factor
9 multicomponent coupling between l-proline or pipecolic acid, aldehydes, and isonitriles is described.
13 orted here had increased CSF alpha-AASA, CSF pipecolic acid, and known or likely pathogenic mutations
15 he urinary elevations in glycine betaine and pipecolic acid (as well as proline) indicated defective
18 report for the first time the occurrence of pipecolic acid betaine (homostachydrine) and its precurs
19 alidate its ability to convert L-lysine to L-pipecolic acid by a cyclodeamination reaction that invol
20 een applied to the synthesis of (R)- and (S)-pipecolic acid derivatives, (+)-beta-conhydrine, (S)-(+)
23 ly identified priming activators azelaic and pipecolic acid, elaborates on the similarity to defense
25 yclic lactam scaffolds were synthesized from pipecolic acid in a sequence of reactions that was initi
29 f saccharopine oxidation, N-oxalylglycine, L-pipecolic acid, L-leucine, alpha-ketoglutarate, glyoxyli
30 tion for this finding is not clear, elevated pipecolic acid levels may serve as a diagnostic marker f
32 e-2-COOH; 4,4'-Bip=4,4'-biphenylalanine; Pip=pipecolic acid) of IC50=0.95 nM and EC50=0.99 nM at hMC5
34 identification of the non-protein amino acid pipecolic acid (Pip), a common Lys catabolite in plants
35 y plant metabolites, salicylic acid (SA) and pipecolic acid (Pip), in the establishment of plant syst
37 Interestingly, some uncommon derivatives of pipecolic acid, such as N-methylpipecolic acid, 4-hydrox
39 the resulting 2,6-cis-6-substituted 4-oxo-l-pipecolic acids to the corresponding 4-hydroxy-L-pipecol
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