ライフサイエンスコーパス: aminobenzoic acid

1 d poly(3,4-ethylenedioxythiopene) and poly(p-aminobenzoic acid).

2 henyl ring whose 5-substituent is N-methyl-p-aminobenzoic acid).

3 d new insights into the crystallization of m-aminobenzoic acid.

4 ite production required the presence of para-aminobenzoic acid.

5 ased mapping approach using stable isotope 2-aminobenzoic acid (2-AA) for rapid "high-level" glycan s

6 A, (Tyrc A) was substituted with the d-Phe-2-aminobenzoic acid (2-Abz) motif in a synthetic analogue

7 Anthranilic acid (2-aminobenzoic acid, 2-AA) has the remarkable property of

8 the fluorescent compound anthranilic acid (2-aminobenzoic acid; 2-AA) to label oligosaccharides prior

9 the virtue of unique anthranilic acid (AA, 2-aminobenzoic acid [2AA]) chemistry for labeling carbohyd

10 rotein G was covalently immobilized onto a 4-aminobenzoic acid (4-ABA) film grafted on the disposable

11 antibody was covalently immobilized onto a 4-aminobenzoic acid (4-ABA) film grafted on the disposable

12 With [3H]benzidine, p-aminobenzoic acid, a NAT1-specific substrate, increased

13 pabB contributes to the biosynthesis of para-aminobenzoic acid, a precursor of both tetrahydrofolate

14 e, KLTFGTVK(Abz)PVQAIAGY(NO2)EWL, in which 2-aminobenzoic acid (Abz) and 3-nitrotyrosine (Y(NO2)) wer

15 FRET peptides containing 2-aminobenzoic acid (Abz) and N-(2,4-dinitrophenyl)ethylen

16 protease (PR) assay was developed in which 2-aminobenzoic acid (Abz) and p-nitrophenylalanine (F(NO2)

17 commercially available anthranilic acids and aminobenzoic acids act as superior catalysts for hydrazo

18 compared undergo reductive amination with 2-aminobenzoic acid and 2-(13)[C6]-aminobenzoic acid, resp

19 ics of N-glycans reductively aminated with 2-aminobenzoic acid and 2-aminobenzamide were compared.

20 ly-Phe-Met-Gln-EDDnp+ ++; where Abz is ortho-aminobenzoic acid and EDDnp is N-(2, 4-dinitrophenyl)eth

21 After derivatisation with p-aminobenzoic acid and sodium cyanoborohydride, the sampl

22 man NAT1 acetylates the sunscreen additive p-aminobenzoic acid and tobacco smoke carcinogen 4-aminobi

23 conditions for an in situ transformation of aminobenzoic acids and their heterocyclic analogues into

24 mmobilized with the carboxyl group of poly(p-aminobenzoic acid) and served as the probe, a target DNA

25 trices, alpha-4-hydroxycyanocinnamic acid, 3-aminobenzoic acid, and 2,5-dihydroxybenzoic acid.

26 nnulation of bis-silyl dienediolate 1 with 2-aminobenzoic acid- and 2-aminobenzamide-derived imines t

27 on of the most sensitive fluorescent label 2-aminobenzoic acid (anthranilic acid, AA) for characteriz

28 coproteins using PNGase F and labeled with 2-aminobenzoic acid (anthranilic acid, AA).

29 ethyl, phenyl, and p-nitrophenyl esters of 2-aminobenzoic acid at 50 degrees C in H(2)O.

30 p-Aminobenzoic acid beta-D-glucopyranosyl ester esterase a

31 aromatic competitors (benzoic acid and para-aminobenzoic acid), but not by nonaromatic LAAO inhibito

32 e ((PQQ)GDH) has been immobilized on [poly(3-aminobenzoic acid-co-2-methoxyaniline-5-sulfonic acid),

33 pho-alpha-D-ribosyl diphosphate (PRPP) and 4-aminobenzoic acid condense together to produce 4-(beta-D

34 The para-aminobenzoic acid-containing peptide albicidin is a path

35 Using 2-aryl-4-aminobenzoic acid derivatives as mimetics for the centra

36 htforward means for the preparation of ortho-aminobenzoic acid derivatives.

37 CNTs were functionalized by treatment with 4-aminobenzoic acid (HOOC-Phe) in the presence of isoamyln

38 In addition, co-administration of 4-aminobenzoic acid hydrazide (4-ABAH), an irreversible in

39 n (PLP), and mice were treated with either 4-aminobenzoic acid hydrazide (ABAH), 40 mg/kg injected in

40 The MPO inhibitor 4-aminobenzoic acid hydrazide reduced peroxidase activity

41 Moreover, a chemical inhibitor of MPO (aminobenzoic acid hydrazide) mimicked the effects of hLF

42 Methimazole, 4-aminobenzoic acid hydrazide, or azide inhibits the react

43 0 cells were incubated with methimazole or 4-aminobenzoic acid hydrazide, which are inhibitors of mye

44 cessfully used to functionalize the aromatic aminobenzoic acids in a chemoselective manner without im

45 and other nutrients (inositol, adenine, or p-aminobenzoic acid) in the transformation medium to devel

46 ctrochemical polymerization of aniline and 3-aminobenzoic acid, in the presence of a dispersion of go

47 re used to carry out a one-pot conversion of aminobenzoic acids into the corresponding amides.

48 procedure for the one-pot transformation of aminobenzoic acids into their amides.

49 mination reaction that takes place when para-aminobenzoic acid is used as a ring precursor of Q(6).

50 osphate, N-acetyl glucosamine, putrescine, p-aminobenzoic acid, L-cysteine and L-glutamine, and horse

51 s present only in the MALDI-CID spectra of 2-aminobenzoic acid-labeled oligosaccharides.

52 ylic acid were investigated for protonated m-aminobenzoic acid (MABAH(+)) with up to 15 water molecul

53 tonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methyl ester (PABAOMe) occurs at the c

54 Protonated 4-aminobenzoic acid molecules (4-ABA) generated by positiv

55 , MFA [mefenamic acid; 2-(2,3-dimethylphenyl)aminobenzoic acid], NFA [niflumic acid; 2-{[3-(trifluoro

56 that creates a specific binding pocket for p-aminobenzoic acid, one of the two DHPS substrates.

57 odified by adsorbing the diazonium salt of 4-aminobenzoic acid onto the PGC, followed by reduction of

58 assay medium, by predepositing N-biotinyl-p-aminobenzoic acid onto the standard sample collection pa

59 olate methanopterin is the condensation of p-aminobenzoic acid (pAB) and 5-phospho-alpha-D-ribosyl-1-

60 ad of an N-riboside in the condensation of p-aminobenzoic acid (pABA) and 5-phospho-alpha-D-ribosyl-1

61 Protonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methyl

62 dent behavior of the zwitterionic molecule p-aminobenzoic acid (PABA) at a Ag(111) electrode surface.

63 he matrix of whole blood and cleaved to para-aminobenzoic acid (pABA) by acid hydrolysis in the prese

64 the observation that exogenously supplied p-aminobenzoic acid (PABA) can antagonize the action of an

65 smodia species, unlike humans, can utilize p-aminobenzoic acid (PABA) for the de novo generation of f

66 Saccharomyces cerevisiae is able to use para-aminobenzoic acid (pABA) in addition to 4-hydroxybenzoic

67 arter unit p-nitrobenzoic acid (pNBA) from p-aminobenzoic acid (pABA) in the biosynthesis of antibiot

68 hromatography are close to those of the para-aminobenzoic acid (pABA) isotopomers; second, substituti

69 .22 nM, indicating that replacement of the p-aminobenzoic acid (pABA) moiety does not diminish cytoto

70 hesis of aromatic amino acids (AroAAs) and p-aminobenzoic acid (PABA) was demonstrated in M. maripalu

71 se (DHPS) catalyzes the condensation of para-aminobenzoic acid (pABA) with 6-hydroxymethyl-7, 8-dihyd

72 Here we show that para-aminobenzoic acid (pABA), a well known precursor of fola

73 tural analog and competitive antagonist to p-aminobenzoic acid (PABA), which is a precursor of folate

74 monstrating selective bacterial uptake: para-aminobenzoic acid (PABA), with uptake in all representat

75 ally active v-tPA, which in turn cleaves a p-aminobenzoic acid (PABA)-peptide adduct to release free

76 tion a conductive polymer poly-(aniline-co-3-aminobenzoic acid) (PANABA) then we immobilized anti-2,4

77 uniqueness among these four compounds, whose aminobenzoic acid precursors differ structurally only in

78 tion with 2-aminobenzoic acid and 2-(13)[C6]-aminobenzoic acid, respectively.

79 electron withdrawing ortho-substituents on 2-aminobenzoic acid resulted in the production of benzoxaz

80 We have inserted beta, gamma and delta -aminobenzoic acid separately into an amyloidogenic pepti

81 e amino acids, tocopherols, pyridoxine and 4-aminobenzoic acid show intense emissions.

82 Studies revealed that PABA/NO's N-methyl-p-aminobenzoic acid substituent is bound to the dinitroben

83 ives of folate, methotrexate (MTX), and para-aminobenzoic acid substrates and a marked preference for

84 ides, including a compound that features a p-aminobenzoic acid subunit.

85 Benzocaine, the ethyl ester of para-aminobenzoic acid that finds an application as a local a

86 re, OCN(-) in aqueous solution reacts with 2-aminobenzoic acid to produce a highly fluorescent deriva

87 obtained for 3'-sialyllactose labeled with 2-aminobenzoic acid using neuraminidase from Clostridium p

88 1.71 g S/d) and 0.17-0.27 g inorganic S/d; p-aminobenzoic acid-validated 24-h urine samples (n = 47)

89 orresponding amides derived from p-(N-methyl)aminobenzoic acid with 2,4-diamino-6-(bromomethyl)pterid

90 biosynthesis, namely, the condensation of p-aminobenzoic acid with phosphoribosylpyrophosphate to fo