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1 eavage of l-kynurenine to give l-alanine and anthranilic acid.
2 dent as was that of a downstream metabolite, anthranilic acid.
3 nt than CI-1040, the cyanoquinoline, and the anthranilic acid.
6 The procedure uses the fluorescent compound anthranilic acid (2-aminobenzoic acid; 2-AA) to label ol
7 ith the matrixes 6-aza-2-thiothymine and 80% anthranilic acid/20% nicotinic acid but not with 3-hydro
10 nhibitors, the high-throughput screening hit anthranilic acid 4, the known benzofuran analogue 5, and
11 ns was made possible by the virtue of unique anthranilic acid (AA, 2-aminobenzoic acid [2AA]) chemist
12 itive fluorescent label 2-aminobenzoic acid (anthranilic acid, AA) for characterization of carbohydra
15 acid derivatives such as N-(p-amylcinnamoyl)anthranilic acid (ACA), which act as slow inhibitors.
17 y amide (CI-1040), two CI-1040 analogues (an anthranilic acid and an N-alkyl amide), and a cyanoquino
19 e report that simple, commercially available anthranilic acids and aminobenzoic acids act as superior
20 xtension of this protocol to the coupling of anthranilic acids and isocyanides leading to medicinally
21 e:tryptophan ratio, and C-reactive protein), anthranilic acid, and 3-hydroxykynurenine were positivel
22 ith N-glycanase F, reductively aminated with anthranilic acid, and fractionated by normal phase high-
23 acid fragment as a suitable isostere for the anthranilic acid appendage of 4, which led to the discov
24 order CI-1040 approximately cyanoquinoline < anthranilic acid approximately U-0126 < alkyl amide.
26 etic derivative of the tryptophan metabolite anthranilic acid, but not l-kynurenine, enhanced product
27 azone ligation were observed when polyvalent anthranilic acid catalysts operating on polyvalent aldeh
34 of the family are sensitive to inhibition by anthranilic acid derivatives such as N-(p-amylcinnamoyl)
35 nds related in structure to flufenamate, all anthranilic acid derivatives, as potential inhibitors of
37 rticularly promising set of analogues is the anthranilic acid esters 63-66 in which the phenyl ring i
38 , followed by N-(9-fluorenylmethoxycarbonyl)-anthranilic acid (Fmoc-anthranilic acid) with an IC(50)
39 sosome-related organelles (gut granules), as anthranilic acid glucosyl esters--not, as previously sur
42 somerism of appropriately substituted N-aryl anthranilic acids has been investigated in the solid sta
47 oceed in 14 steps from protected tryptophan, anthranilic acid, leucine, and alanine in 7% overall yie
48 r X-ray complex structures of representative anthranilic acid ligands bound to AcpS are described in
49 ence of BBA5 were synthesized to include the anthranilic acid/nitrotyrosine fluorescence quenching pa
50 stered tranilast, N-(3,4-dimethoxycinnamoyl) anthranilic acid, on histologic and histomorphometric ch
51 een the indole-nitrogen of tryptophan and an anthranilic acid residue, and a high yielding macrolacta
52 e synthetic derivative of the Trp metabolite anthranilic acid, reversed paralysis in mice with experi
53 are also important interaction sites for the anthranilic acid S0100176 (N-benzyl-N-pyridin-3-ylmethyl
55 rally active class of MetAP2 inhibitors, the anthranilic acid sulfonamides exemplified by A-800141, w
56 reversible inhibitors of MetAP2, a series of anthranilic acid sulfonamides with micromolar affinities
57 econd step (microwave-assisted reaction with anthranilic acid) takes approximately 14 h in total to c
60 serum levels of kynurenine, kynurenic acid, anthranilic acid, tryptophan, nicotinamide and N1-methyl
61 s can be reacted with commercially available anthranilic acids under microwave irradiation conditions
63 oxyanthranilic acid, and 3-hydroxykynurenine:anthranilic acid were significant discriminating variabl
64 Higher concentrations of nicotinamide and anthranilic acid were, however, associated with a lower
65 metabolites: kynurenine, kynurenic acid, and anthranilic acid, were substantially, but differentially
66 also inhibited by ACA, ONO-RS-082, and Fmoc-anthranilic acid, whereas the Na(+)/citrate transporter
68 renylmethoxycarbonyl)-anthranilic acid (Fmoc-anthranilic acid) with an IC(50) value of approximately
69 ng PLP, kynurenine, HK, kynurenic acid (KA), anthranilic acid, xanthurenic acid (XA), and 3-hydroxyan
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