ライフサイエンスコーパス: phenylacetic acid

1 rs such as dopamine and dopac (3,4-dihydroxy-phenylacetic acid).

2 e+furaneol, eugenol, gamma-dodecalactone and phenylacetic acid.

3 operationally simple protocol for assembling phenylacetic acids.

4 s observed in incubations with n-caproic and phenylacetic acids.

5 ate (0.63), furan-2-carbaldehyde (0.33), and phenylacetic acid (0.49), while yeasts displayed correla

6 cetaldehyde (0.37), ethyl hexanoate (-0.59), phenylacetic acid (-0.50), and furan-2-carbaldehyde (-0.

7 hydroxyphenyl)-valeric acid (26.2mug/ml) and phenylacetic acid (19.5mug/ml) reached the highest conce

8 tors >/=16) were beta-damascenone, furaneol, phenylacetic acid, 2-phenylethanol, 4-vinylguaiacol, sot

9 ed the test compound 2-(3-chlorophenylamino) phenylacetic acid (23CPPA) by oral gavage for 26 weeks,

10 Phenylacetic acid 6 is formed in some cases but under th

11 (5-formylfuran-2-yl)methyl acetate (68%), 2-phenylacetic acid (69%) and 4-hydroxy-3-methoxybenzaldeh

12 e with the dilithium enediolate derived from phenylacetic acid affords a tetralithio aggregate compri

13 (II)-catalyzed C-H olefination reaction with phenylacetic acid and 3-phenylpropionic acid substrates,

14 icillin (penicillin G) side-chain to produce phenylacetic acid and 6-aminopenicillanic acid (6-APA).

15 tep sequence starting from readily available phenylacetic acid and pivalic acid through sequential fu

16 cid, pantolactone+furaneol, p-vinylguaiacol, phenylacetic acid and vanillin were the most important a

17 Arabidopsis CYP79A2 mutants that overproduce phenylacetic acid and was lost in knockout mutants of UD

18 offers a catalytic route to ortho-deuterated phenylacetic acids and benzoic acids and demonstrates th

19 Phenylacetic acids and benzoic acids are suitable substr

20 also found for the acidities of substituted phenylacetic acids and benzoic acids.

21 A new approach to the synthesis of phenylacetic acids and esters has been developed via the

22 oside; we found derivatives of benzoic acid, phenylacetic acid, and phenyl propionic acid in the ceca

23 sulfate, cresol, glycine, P-cresol sulfate, phenylacetic acid, and stearoylcarnitine).

24 ydroxycinnamic acids, phenylpropionic acids, phenylacetic acids, and simple phenols were identified.

25 Benzoate and phenylacetic acid are competitive inhibitors, with Kis v

26 osylglycerol, with one metabolite containing phenylacetic acid as the acyl component of the ester.

27 nd was secondary to an impaired A. baumannii phenylacetic acid catabolism pathway, which led to accum

28 n a shunt product from aerobic CoA-dependent phenylacetic acid catabolism that is salvaged by the ded

29 entration dependences (zero order in o-CF(3)-phenylacetic acid concentration, zero order in oxygen pr

30 meta-C-H olefination of phenylacetic acid derivatives has been achieved using a

31 xtensive study of the binding of a series of phenylacetic acid derivatives has been carried out.

32 for the direct carboxylation of benzoic and phenylacetic acid derivatives to form dicarboxylic acids

33 ation-assisted ortho C-H bond olefination of phenylacetic acid derivatives with unactivated, aliphati

34 oketones from readily available, inexpensive phenylacetic acid derivatives.

35 dopamine (DA) and its metabolite dihydroxy-O-phenylacetic acid (DOPAC) were extracted from medial pre

36 A new convenient and scalable synthesis of phenylacetic acids has been developed via the iodide cat

37 lbenzyl)-(2,2-diphenylethyl)amino]propyloxy] phenylacetic acid hydrochloride (GW3965)].

38 nd that toluene can react with CO(2) to form phenylacetic acid in one step without any catalyst with

39 A series of phenylacetic acids, including mandelic acid and phenylgl

40 er, the catalytic thermal decarboxylation of phenylacetic acids is presented.

41 3,5-dichloro-4-(4-hydroxy-3-isopropylphenoxy)phenylacetic acid (KB-141) on the expression of TR agoni

42 g with dimethylmalate or its inhibition with phenylacetic acid led to proportional changes in insulin

43 Inhibition of PC by 5 mm phenylacetic acid markedly lowered glucose-induced insul

44 l oxide, 2-ethyl hexanol, phenylethanol, and phenylacetic acid may be important contributors to the f

45 and para with either (S)-alpha-methoxy-alpha-phenylacetic acid (MPA) or (S)-phenylglycine methyl este

46 Two natural auxins, phenylacetic acid (PAA) and indole-3-acetic acid (IAA),

47 lly described and includes the natural auxin phenylacetic acid (PAA) and the potential SA precursor b

48 oup play roles in metabolic pathways such as phenylacetic acid (PAA) catabolism, the Hut system, the

49 ent metabolism of dietary phenylalanine into phenylacetic acid (PAA) is critical in phenylacetylgluta

50 athway leading to a less well studied auxin, phenylacetic acid (PAA), remains unclear.

51 espond to fenofibric acid and a novel potent phenylacetic acid peroxisome proliferator-activated rece

52 Mcl-1 inhibitors featuring an alpha-hydroxy phenylacetic acid pharmacophore or bioisostere.

53 ized with or without the methyl group on the phenylacetic acid ring and with various substitutions on

54 es demonstrated that the methyl group on the phenylacetic acid ring is required for COX-2 selectivity

55 (dopamine metabolite neurotransmitter), and phenylacetic acid (sodium salt form; treatment of urea c

56 ctron interactions are not possible with the phenylacetic acids, this indicates that the acidities ar

57 Oxidations of phenylacetic acid to benzaldehyde, benzyl alcohol to ben

58 ed the elaboration of commercial fluorinated phenylacetic acids to 2-(fluoroaryl)glutaric acids with

59 n) into hydroxybenzoic, phenylpropanoic, and phenylacetic acids upon digestion (35.54 ug/mg DW).

60 Phenylacetic acid was associated with length for age z s

61 The meta-C-H arylation of free phenylacetic acid was realized using 2-carbomethoxynorbo

62 Free phenylacetic acids were also allylated utilizing similar

63 d(II)-catalyzed C-H olefination reactions of phenylacetic acids when mono-N-protected amino acids are

64 One of the peaks was shown to represent phenylacetic acid, which has implications for the mechan

65 gen excretion via combination of PBA-derived phenylacetic acid with glutamine to form phenylactylglut

66 ydroxylation of a broad range of benzoic and phenylacetic acids with an industry-compatible oxidant,

67 itates dietary phenylalanine conversion into phenylacetic acid, with subsequent host generation of PA