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1 s the 1,2-dihydroxylation of anthranilate (2-aminobenzoate).
2 he Marshall-Bratton reaction to quantitate p-aminobenzoate.
3 the cross-linker N-succinimidyl(4-iodoacetyl)aminobenzoate.
4 fold condensation of 3,4-bis(alkoxy)phenyl 4-aminobenzoates/3,4,5-tris(alkoxy) phenyl 4-aminobenzoate
5 tional enzyme involved in the synthesis of p-aminobenzoate, a central component part of folate cofact
6                  Kinetic analyses indicate 4-aminobenzoate and 4-hydroxybenzoate are preferred acyl s
7 BS3 favors 4-substituted benzoates such as 4-aminobenzoate and 4-hydroxybenzoate, with moderate activ
8  4-amino-4-deoxychorismate, a precursor of p-aminobenzoate and folate in microorganisms.
9  4-amino-4-deoxychorismate, a precursor of p-aminobenzoate and folic acid in microorganisms.
10 esis precursors: pABAGlu was hydrolysed to p-aminobenzoate and glutamate, and dihydropterin-6-aldehyd
11 functionalization protocols to access aryl 2-aminobenzoates and 2-substituted benzoxazinone derivativ
12 rismate in the biosynthesis of tryptophan, p-aminobenzoate, and enterobactin, respectively, and are e
13 ith pyranoradine tetraphosphate, potassium p-aminobenzoate, and escin as compared with vehicle contro
14  nonheme di-iron oxygenase, AurF, converts p-aminobenzoate (Ar-NH(2), where Ar = 4-carboxyphenyl) to
15 on also resulted from a normally avirulent p-aminobenzoate auxotroph.
16 s of abgT and medium-copy levels of abgAB, p-aminobenzoate auxotrophs grew on 50 nM p-aminobenzoyl-gl
17  structural protein enabling the growth of p-aminobenzoate auxotrophs on exogenous p-aminobenzoyl-glu
18 o the medium-copy-number plasmid pACYC184; p-aminobenzoate auxotrophs transformed with the clone enco
19            In a portion of IJs grown on para-aminobenzoate auxotrophs, X. nematophila does not exhibi
20 bstituted benzotriazepinones from 4-acetyl-3-aminobenzoate based on aza-amino acid chemistry and diff
21 , p-hydroxybenzoate, and substrate analog, p-aminobenzoate, binding to p-hydroxybenzoate hydroxylase
22 ulosis and leprosy, and an inhibitor of para-aminobenzoate biosynthesis.
23 benzoyl-glutamate, followed by cleavage to p-aminobenzoate by a protein composed of subunits encoded
24 nteraction with Tyr63 at the end of the para-aminobenzoate channel.
25 ntitate lipoic acid released from lipoyl-N-p-aminobenzoate correlated excellently with results obtain
26                                      Butyl 4-aminobenzoate derivatives of Glc(4) and the internal sta
27        A HPLC method associated with butyl-p-aminobenzoate derivatization has been developed for the
28                                        The 2-aminobenzoate esters hydrolyze with similar rate constan
29             The addition of nonradioactive p-aminobenzoate has no effect.
30 e self-condensation of N-benzylated phenyl p-aminobenzoates in the presence of LiHMDS to yield three-
31                              Anthranilate (2-aminobenzoate) is an important intermediate in tryptopha
32                                        For p-aminobenzoate, its three most intense Raman features, du
33 ), a maleimidocaproyl-valine-citrulline-para-aminobenzoate linker, and the antimicrotubule cytotoxin
34            However, despite a vast number of aminobenzoate metal complexes having been reported, and
35                                          The aminobenzoate moiety stacks on a guanine base, whereas t
36                                            p-Aminobenzoate N-oxygenase (AurF) from Streptomyces thiol
37         In both organisms, the addition of p-aminobenzoate or 5-formyltetrahydrofolate in the externa
38                             Plants produce p-aminobenzoate (pABA) in chloroplasts and use it for fola
39                          Plants synthesize p-aminobenzoate (pABA) in chloroplasts and use it for fola
40      Dihydropteroate synthase incorporates p-aminobenzoate (pABA) into dihydropteroate, the precursor
41  plants, the last step in the synthesis of p-aminobenzoate (PABA) moiety of folate remains to be eluc
42  It is not known how plants synthesize the p-aminobenzoate (PABA) moiety of folates.
43 us catalyzes the six-electron oxidation of p-aminobenzoate (pABA) to p-nitrobenzoate (pNBA).
44 ADD) is involved in the biosynthesis of para-aminobenzoate (pABA), an essential component of the fola
45   Plants synthesize folate from pteridine, p-aminobenzoate (PABA), and glutamate moieties.
46    Folates are synthesized from pteridine, p-aminobenzoate (PABA), and glutamate precursors.
47 A key precursor for folate synthesis is para-aminobenzoate (pABA).
48 um tuberculosis by mimicking the substrate p-aminobenzoate (PABA).
49            Here we show that streptococcal 4-aminobenzoate/para-amino benzoic acid (pABA) is required
50 ropoxy, s-butoxy, and t-butoxy groups on a p-aminobenzoate peptidyl carrier protein thioester interme
51    X. nematophila mutants defective for para-aminobenzoate, pyridoxine or l-threonine biosynthesis ex
52 tant PHBH, with bound p-hydroxybenzoate or p-aminobenzoate, reveal a chain of proton donors and accep
53 n in the NADH complex to stack against the p-aminobenzoate ring of the folate.
54 I) or Ir(III) complexes with mesalazine or 3-aminobenzoate Schiff bases of the general formulas [Ru(p
55  chip wells via N-succinimidyl (4-iodoacetyl)aminobenzoate (SIAB) chemistry.
56 ence quenching study indicates that phenyl 2-aminobenzoate specifically detects Fe(II) ions, exhibiti
57 so devised a green method for synthesizing 2-aminobenzoate-subtituted paracetamol through a decarboxy
58    An Escherichia coli strain deficient in p-aminobenzoate synthesis was mutagenized, and derivatives
59 1-(RS)-carboxy-3-phenylpropyl]-Ala-Ala-Tyr-p-aminobenzoate, the binding of which we have shown to be
60 constitute the CysS-catalyzed reaction, on p-aminobenzoate thioester substrates, and demonstrate that
61 us catalyzes the six-electron oxidation of p-aminobenzoate to p-nitrobenzoate and contains the EX2HX6
62         This enzyme converts anthranilate (2-aminobenzoate) to catechol with insertion of both atoms
63 viding either shikimate or a mixture of para-aminobenzoate, tryptophan, tyrosine, and phenylalanine,
64 cture of l-amino acid oxidase complexed with aminobenzoate, Tyr372 hydrogen bonds with the carboxylat
65  whereas [(3)H]folate synthesis from p-[(3)H]aminobenzoate was extensive.
66 anium oxo cluster, Ti6O6(OCH3)6(AB)6 (AB = 4-aminobenzoate), which was linked with benzene-1,4-dialde
67  step in the conversion of chorismate into p-aminobenzoate, which is incorporated into folic acid.
68  falciparum was reversed by treatment with p-aminobenzoate, which suggests that the shikimate pathway
69 4-aminobenzoates/3,4,5-tris(alkoxy) phenyl 4-aminobenzoates with 1,3,5-triformylphloroglucinol and ch