戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 mediated nucleophilic attack by water on the phosphoester.
2 prolactone, a cyclic carbonate, and a cyclic phosphoester.
3 18)O)(2)-ATP from ADP and the C25-((18)O)(2)-phosphoester.
4 d is not inhibited by Etn, choline, or their phosphoesters.
5 er than those of the six-membered monocyclic phosphoester, 2-ethoxy-1,3,2-dioxaphosphinane 2-oxide.
6 d subsequent deprotection of the cyano ethyl phosphoester afforded the target compounds in 16-21 % ov
7 J mol(-1) higher than that of standard sugar phosphoesters and even slightly greater than the B,y-pho
8 uctures and mechanistic requirements between phosphoesters and peptides during hydrolysis, the study
9                                              Phosphoesters and phosphonodiesters were synthesized and
10 ter oxygen, such that diverse aryl and alkyl phosphoesters are turned over with similar catalytic eff
11 eural network potentials (NNPs) to study the phosphoester bond formation in water.
12 nformational transition, nucleotide binding, phosphoester bond formation, and dissociation steps.
13 ine with the P(alpha)-O(5') bond to catalyse phosphoester bond hydrolysis.
14  be involved in metal-dependent catalysis of phosphoester bond hydrolysis.
15               Changing an oxygen atom of the phosphoester bond in phosphopeptides by a sulfur atom en
16 sphopantetheine swinging arm bound through a phosphoester bond to Ser(354) of the intermediate domain
17 redox-active prosthetic groups attached by a phosphoester bond to threonine residues in subunits NqrB
18 it cleaves a pyrophosphate bond instead of a phosphoester bond, and its substrate contains nucleoside
19 ecule to the phosphorus atom of the scissile phosphoester bond, with the attacking water being simult
20                                          DNA phosphoester bonds are exceedingly resistant to hydrolys
21 rotein kinases both catalyze the transfer of phosphoester bonds from nucleotides to proteins.
22 nzymatic activity in addition to cleavage of phosphoester bonds in RNA.
23  other biochemically important "high-energy" phosphoester bonds.
24 amolecular transesterification, we installed phosphoester breaking points with similar hydroxyethoxy
25  or a closely related analog to catalyze RNA phosphoester cleavage, producing a rate enhancement of a
26                UTP-gamma-aryl and cycloalkyl phosphoesters displayed only intermediate P2Y(6) recepto
27  Qualitatively, the outcome is determined by phosphoester elongation and siloxane contraction along t
28               LPA analogs including a cyclic phosphoester form and ether-linked forms of LPA activate
29 rithiamine interferes with cellular thiamine phosphoester homeostasis is not entirely clear.
30 ructures provide models for intermediates in phosphoester hydrolysis and suggest specific mechanistic
31 bitors toward the hydrolysis of the peptide, phosphoester hydrolysis by peptidases is thus not expect
32                            The mechanisms of phosphoester hydrolysis by these enzymes are beginning t
33 er of a large class of enzymes that catalyze phosphoester hydrolysis using a phosphoaspartate-enzyme
34 ously capable of catalyzing carboxyester and phosphoester hydrolysis.
35 d oximolysis rates for acetylthiocholine and phosphoester hydrolysis.
36 edominantly C2'-endo to C3'-endo when the 3'-phosphoester is replaced by a phosphoramidate group.
37 s B and C are bound to threonine residues by phosphoester linkages.
38 ing of small molecules with the 2',3' cyclic phosphoester linkages.
39                                       The -2 phosphoester or nucleotide is found to increase the reac
40 f the acyloxymethyl and isopropyloxycarbonyl phosphoester prodrugs of CDNs.
41 ecules in solution populate a wider range of phosphoester ring conformations than in R32 and P3 cryst
42 al modeling of the six-membered 3',5'-cyclic phosphoester ring derived from deoxyribose indicated str
43          The results imply a highly flexible phosphoester ring that may be relevant to the function o
44                      Our six-membered cyclic phosphoester ring-opening polymerization strategy is dem
45 se library of hyperbranched unsaturated poly(phosphoester)s that allow efficient scavenging of single
46             Both symmetric and antisymmetric phosphoester stretching modes are highly sensitive to P-
47 ns involving inorganic phosphate and organic phosphoesters such as phospholipids, phosphorylated prot
48 loyed as termini (versus prior phosphono- or phosphoester termini) in designs of trans-AB-porphyrins
49  at 821 cm-1is demonstrated as diagnostic of phosphoester torsions alpha and zeta in the gauche+ rang
50 ozyme promotes self-cleavage via an internal phosphoester transfer reaction involving the adjacent 2'
51 e in the active site pocket to carry out the phosphoester transfer reaction.
52 ng the 2'-hydroxyl to initiate the reaction (phosphoester transfer).
53 d in other antineoplastic agents influencing phosphoester transfer.
54 structures that promote cleavage by internal phosphoester transfer.
55 l transfer potential of tertiary steroid C25-phosphoesters, which is 20 kJ mol(-1) higher than that o
56 w DSPs accomplish similar reaction rates for phosphoesters, whose reactivity (i.e., pK(a) of the leav
57              Fascinatingly, even challenging phosphoesters with poor leaving groups, which were found