ライフサイエンスコーパス: p-aminobenzoic acid

1 ophenyl ring whose 5-substituent is N-methyl-p-aminobenzoic acid).

2 zed poly(3,4-ethylenedioxythiopene) and poly(p-aminobenzoic acid).

3 This study evaluates 2-[18F]F-p-aminobenzoic acid (2-[18F]F-PABA), a bacteria-specific

4 With [3H]benzidine, p-aminobenzoic acid, a NAT1-specific substrate, increase

5 After derivatisation with p-aminobenzoic acid and sodium cyanoborohydride, the sam

6 human NAT1 acetylates the sunscreen additive p-aminobenzoic acid and tobacco smoke carcinogen 4-amino

7 immobilized with the carboxyl group of poly(p-aminobenzoic acid) and served as the probe, a target D

8 p-Aminobenzoic acid beta-D-glucopyranosyl ester esterase

9 to be a direct precursor in the synthesis of p-aminobenzoic acid (folate biosynthesis), p-hydroxybenz

10 s and other nutrients (inositol, adenine, or p-aminobenzoic acid) in the transformation medium to dev

11 phosphate, N-acetyl glucosamine, putrescine, p-aminobenzoic acid, L-cysteine and L-glutamine, and hor

12 rotonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methyl ester (PABAOMe) occurs at the

13 novel binding pocket for the CHO-H(4)folate p-aminobenzoic acid moiety directly affects how bent the

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

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

16 ) covalently immobilized onto electrografted p-aminobenzoic acid (p-ABA).

17 sing a glassy carbon electrode modified with p-aminobenzoic acid, p-aminothiophenol and gold nanopart

18 folate methanopterin is the condensation of p-aminobenzoic acid (pAB) and 5-phospho-alpha-D-ribosyl-

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

20 Protonation of p-aminobenzoic acid (PABA) and p-aminobenzoic acid methy

21 endent behavior of the zwitterionic molecule p-aminobenzoic acid (PABA) at a Ag(111) electrode surfac

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

23 lasmodia species, unlike humans, can utilize p-aminobenzoic acid (PABA) for the de novo generation of

24 starter unit p-nitrobenzoic acid (pNBA) from p-aminobenzoic acid (pABA) in the biosynthesis of antibi

25 0.22 nM, indicating that replacement of the p-aminobenzoic acid (pABA) moiety does not diminish cyto

26 nthesis of aromatic amino acids (AroAAs) and p-aminobenzoic acid (PABA) was demonstrated in M. maripa

27 uctural analog and competitive antagonist to p-aminobenzoic acid (PABA), which is a precursor of fola

28 rst members of a new class of broad-spectrum p-aminobenzoic acid (PABA)-based antibiotics.

29 ically active v-tPA, which in turn cleaves a p-aminobenzoic acid (PABA)-peptide adduct to release fre

30 Tapcin is a mixed p-aminobenzoic acid (PABA)-thiazole with a rare tri-thia

31 fied, and only eight were not bioaccessible (p-aminobenzoic acid, sinapic acid, pinobanksin, isorhamn

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

33 osides, including a compound that features a p-aminobenzoic acid subunit.

34 3-1.71 g S/d) and 0.17-0.27 g inorganic S/d; p-aminobenzoic acid-validated 24-h urine samples (n = 47

35 in biosynthesis, namely, the condensation of p-aminobenzoic acid with phosphoribosylpyrophosphate to