ライフサイエンスコーパス: hydrolysable

1 The addition of a non-hydrolysable 2'-deoxycytosine-5'-[(alpha,beta)-methyleno

2 nolics, extractable (8855.50mg GAE/100g) and hydrolysable (7005.51mg GAE/100g), than the other variet

3 ly added topo II in a manner that depends on hydrolysable adenosine triphosphate (ATP), whereas an in

4 The non-hydrolysable ADP analogue, ADPbetaS, acting at P2Y1 rece

5 ion to ATP, a diminished response to its non-hydrolysable analog alphabetaMeATP, and a reduced contra

6 ty does not occur in the presence of the non-hydrolysable analog ATP-gammaS.

7 des, ADP, and adenylyl-imidodiphosphate (non-hydrolysable analog of ATP).

8 '-[(beta,gamma)-imido]triphosphate, a poorly hydrolysable analog of GTP.

9 AMP and hydrolysable analogs of cAMP inhibited TbTOR4 expression

10 by either adenosine (100 microM) or its non-hydrolysable analogue 2-chloroadenosine (CADO; 0.1-5.0 m

11 However, in the presence of ATP, or the non-hydrolysable analogue 5'-adenylyl beta,gamma-imidodiphos

12 as the effect of ATP was mimicked by the non-hydrolysable analogue 5'-adenylylimidodiphosphate (AMP-P

13 It was found that AMP, ADP and the non-hydrolysable analogue adenylyl imidodiphosphate (AMP-PNP

14 In the presence of non-hydrolysable analogue beta,gamma-imidoadenosine 5'-triph

15 n with Rac bound to either GDP or the slowly hydrolysable analogue GMPPNP show that the switch region

16 to NaV1.9, is upregulated by GTP and its non-hydrolysable analogue GTP-gamma-S, but not by GDP.

17 Upon binding of ADPNP (non-hydrolysable analogue of ATP), by PcrA, a conformational

18 Intracellular dialysis with the non-hydrolysable analogue of ATP, 5'-adenylylimidodiphosphat

19 te both in the presence and absence of a non-hydrolysable analogue of ATP, ADPNP.

20 The non-hydrolysable analogue of ATP, AMP-PNP, did not substitut

21 vator, forskolin, and the cell-permeable non-hydrolysable analogue of cyclic adenosine monophosphate

22 lso form in the presence of ATPgammaS, a non-hydrolysable analogue of the ATP required for translocat

23 The presence of ATP or a non-hydrolysable analogue, ADPNP, during limited proteolysis

24 h adenylyl imidodiphosphate (AMP-PNP), a non-hydrolysable analogue.

25 cells internally perfused with cAMP and non-hydrolysable analogues of cAMP.

26 Introducing non-hydrolysable analogues of GTP into the cytosolic compart

27 in the presence or absence of ATP and of non-hydrolysable analogues.

28 A total of 120 compounds, including hydrolysable and condensed tannins, flavonoids and pheno

29 A wide range of different hydrolysable and poorly hydrolysable nucleoside triphosp

30 tor latrunculin, even in the presence of non-hydrolysable ATP (AMP-PNP).

31 e annealing activity is inhibited by the non-hydrolysable ATP analog (adenosine 5'-O-(thiotriphosphat

32 d GQ unfolding by BLM in the presence of non-hydrolysable ATP analogs, which has implications for the

33 nduced by the combination of peptide and non-hydrolysable ATP analogs.

34 , a G-protein activator (GTPgammaS) or a non-hydrolysable ATP analogue (AMPPcP).

35 The inability of the non-hydrolysable ATP analogue 5'-adenylylimidodiphosphate (A

36 trated that, following dialysis with the non-hydrolysable ATP analogue 5'-adenylylimidodiphosphate (A

37 The non-hydrolysable ATP analogue adenylylimidodiphosphate (AMP(

38 amp in the closed conformation using the non-hydrolysable ATP analogue ADPNP (5'-adenylyl beta,gamma-

39 of ATP, or in the presence of ADP or the non-hydrolysable ATP analogue AMP-PNP, the interaction with

40 B glutamate (i.e. E1371) or by using the non-hydrolysable ATP analogue AMP-PNP.

41 edly inhibited response to AMP-PNP, a poorly hydrolysable ATP analogue that can nearly lock open the

42 g can be achieved in the presence of the non-hydrolysable ATP analogue, 5'-adenylyl beta,gamma-imidod

43 opyrum pernix in complexes with ADP or a non-hydrolysable ATP analogue, ADPNP.

44 resent the structure of EHD2, bound to a non-hydrolysable ATP analogue, and provide evidence consiste

45 mediated dissociation was abrogated by a non-hydrolysable ATP analogue, indicating that chaperone act

46 y adenylyl imidodiphosphate (AMP-PNP), a non-hydrolysable ATP analogue, is markedly diminished in K46

47 DNA substrates either with or without a non-hydrolysable ATP analogue.

48 form tubulin rings in the presence of a non-hydrolysable ATP analogue.

49 which was increased by the presence of a non-hydrolysable ATP analogue.

50 atch pipette or when substituted for the non-hydrolysable ATP analogues 5'-adenylylimidodiphosphate,

51 Previous studies using non-hydrolysable ATP analogues and hydrolysis-deficient cyst

52 ic depletion of eATP or competition with non-hydrolysable ATP analogues induced pathogenesis-related

53 These movements are driven by binding of non-hydrolysable ATP analogues to a monomer of SecA in assoc

54 ame ring, formed with either ATP, ADP or non-hydrolysable ATP analogues, suggesting that the specific

55 anion selectivity sequence, requirement for hydrolysable ATP) in Pgp-expressing cells were different

56 currents from inhibition needs intracellular hydrolysable ATP, presumably for PIP(2) resynthesis.

57 One such factor has been identified as hydrolysable ATP-Mg although the mechanism for ATP funct

58 ing, while formation of the DH also requires hydrolysable ATP.

59 o bind RNA, and RNA binding was prevented by hydrolysable ATP.

60 re beta,gamma-complex in the presence of non-hydrolysable ATPgammaS, indicating that an intact RecA f

61 phosphate (Ins 2,4,5-P3) is known to be less hydrolysable by the InsP3-5-phosphatase than is Ins 1,4,

62 The high soil acid-hydrolysable C to total organic C ratio at bamboo planta

63 amboo increased microbial C and N, soil acid-hydrolysable C, recalcitrant C, and soluble organic C of

64 of ICa to cAMP could be reversed by the non-hydrolysable cAMP analogue 8-Br-cAMP or the phosphodiest

65 tylmethylxanthine (IBMX; 10 microM), the non-hydrolysable cAMP analogue 8-bromo-cAMP (1 mM), or the a

66 Thus, carnosine, or non-hydrolysable carnosine analogs, may represent a new clas

67 light, or by dialysing the cells with a non-hydrolysable cGMP analogue.

68 focussed on the integration of more or less hydrolysable components to modulate degradation rates.

69 Hydrolysable ester conjugates of PEG(1)(0)(0)(0), PEG(2)

70 In the absence of a hydrolysable form of ATP, the distance across the subuni

71 nosine, or intracellular infusion of the non-hydrolysable GTP analog 5'-guanylylimidodiphosphate (Gpp

72 A cold-stable tubulin polymer with the non-hydrolysable GTP analogue GMPCPP, containing semi-conser

73 e crystal structure of Cdc42Hs, with the non-hydrolysable GTP analogue GMPPNP, in complex with the GA

74 rhoGAP, in which Cdc42Hs is bound to the non-hydrolysable GTP analogue GMPPNP.

75 man gamma-tubulin bound to GTP-gammaS (a non-hydrolysable GTP analogue).

76 orm a continuous surface stabilized by a non-hydrolysable GTP analogue, and Sar1 has rearranged from

77 otriphosphate (GTPgammaS, 100 microM), a non-hydrolysable GTP analogue, mimicked the FMRFamide inhibi

78 2-Ran x GppNHp complex where GppNHp is a non-hydrolysable GTP analogue.

79 produced by intracellular dialysis with non-hydrolysable GTPgammaS.

80 Non-hydrolysable guanine nucleotide analogues (GDP-beta-S an

81 gs made with an electrode containing the non-hydrolysable guanosine triphosphate analogue, guanosine

82 lly related analogues that are poorly or non-hydrolysable is sufficient to induce opening.

83 e range of different hydrolysable and poorly hydrolysable nucleoside triphosphates were used to eluci

84 import could no longer be inhibited with non-hydrolysable nucleotide analogues, indicating that no Ra

85 loenzymes, but only when the activator and a hydrolysable nucleotide was added and the DNA was opened

86 Although non-hydrolysable nucleotides are sufficient for channel func

87 urve, different concentrations of the poorly hydrolysable nucleotides, ATPgammaS and ADPbetaS, could

88 with minimal effect upon the addition of non-hydrolysable nucleotides.

89 This study is the first to demonstrate hydrolysable PEG drug ester conjugates are a promising a

90 than 15% to total antioxidant activity, and hydrolysable polyphenols give a major contribution; carc

91 Pre-extraction of enzymatically-hydrolysable starch and xylan reduced the release of fur

92 e of the enzyme co-crystallised with the non-hydrolysable substrate analogue 2,6-diketo-nona-1,9-dioi

93 The positions of the inhibitor (the non-hydrolysable substrate analogue dUDP) and the metal ion

94 the C.jejuni dUTPase in complex with the non-hydrolysable substrate analogue dUpNHp allows us to defi

95 as been crystallized in complex with the non-hydrolysable substrate analogue S-(2-oxo)pentadecyl-CoA,

96 rmophilus elongation complex (EC) with a non-hydrolysable substrate analogue, adenosine-5'-[(alpha,be

97 For both high total phenolic, hydrolysable tannin and anthocyanins contents, as well a

98 ort that low dose of chebulagic acid (CA), a hydrolysable tannin found in myrobalan fruits can inhibi

99 Oenothein B, a dimeric hydrolysable tannin, dose-dependently induced a number o

100 the previously identified proanthocyanidin, hydrolysable tannin, flavonoid, and phenolic acid classe

101 enolic acids (13), monomeric flavonoids (8), hydrolysable tannins (12), proanthocyanidin (1) and anth

102 the contents of total phenolics (7.2-17.2%), hydrolysable tannins (16.7-59.5%) and anthocyanins (11.7

103 identification of up to 39 chemicals, being hydrolysable tannins and anthocyanins the predominant st

104 Hydrolysable tannins and ellagic acid were identified as

105 entified were from the quercetin family, the hydrolysable tannins and fatty acids and their derivativ

106 noids, phenolic acids and related compounds, hydrolysable tannins and related compounds, and other ph

107 te a sizeable fraction of phenolic acids and hydrolysable tannins in the whole fruit.

108 punicalagin and alpha-punicalagin (the major hydrolysable tannins) against clarification were similar

109 itosan and xanthan gum)] on total phenolics, hydrolysable tannins, anthocyanins and antioxidant activ

110 a key intermediate in the synthesis of plant hydrolysable tannins, is also a primary anti-inflammator

111 -d-glucose, a precursor for the synthesis of hydrolysable tannins.