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

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

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

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

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

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

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

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

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

14 Phenylacetic acids and benzoic acids are suitable substr

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

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

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

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

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

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

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

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

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

24 oketones from readily available, inexpensive phenylacetic acid derivatives.

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

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

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

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

29 3,5-dichloro-4-(4-hydroxy-3-isopropylphenoxy)phenylacetic acid (KB-141) on the expression of TR agoni

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

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

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

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

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

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

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

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

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

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

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

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

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

43 Free phenylacetic acids were also allylated utilizing similar

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

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

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