ライフサイエンスコーパス: photoreaction

1 sin and bacteriorhodopsin during the primary photoreaction.

2 reduced the extent of aggregation caused by photoreaction.

3 6 seen in L are not affected by the L --> L' photoreaction.

4 them from those residues not affected by the photoreaction.

5 0(2) mumol.m(2).s(-1)) is sufficient for the photoreaction.

6 l intermediate that was preferred during the photoreaction.

7 nd DMSO, leading to efficient intramolecular photoreaction.

8 Y8) pKa has a profound impact on the forward photoreaction.

9 nnected conformer in the repellent signaling photoreaction.

10 connected states in the attractant signaling photoreaction.

11 to electrochemically detect products of the photoreaction.

12 d in the development of new highly efficient photoreactions.

13 psoralen may be involved in protein-psoralen photoreactions.

14 o protons and the execution of multielectron photoreactions.

15 tion and fail to undergo the Norrish Type II photoreactions.

16 ted for their efficacy in hydrogen-producing photoreactions.

17 re bound by the host and were protected from photoreactions.

18 The initial byproduct of the photoreaction, 2-naphthoquinone-3-methide, reacts rapidl

19 The initial byproduct of the photoreaction, 4-hydroxyquinone-2-methide, undergoes rap

20 We found that the primary photoreaction and the formation of the K-like photo inte

21 e for hydrogen atom or proton abstraction in photoreactions and allows to assess the influence of exp

22 mplexation with SRI, i.e., for wild-type SRI photoreactions and attractant and 2-photon repellent pho

23 ze but also for studying processes including photoreactions and mass transport at the nanoscale, self

24 es can be employed to control and manipulate photoreactions and thereby serve as an efficient tool fo

25 1)O2) in dissolved organic matter-sensitized photoreactions, and identification of oxidative modifica

26 retinal bound to rhodopsin and its ultrafast photoreaction are active topics of research.

27 Relative nucleophilicities in the photoreactions are also similar to those of comparable b

28 nt from the changes observed in the BR --> K photoreaction at the same temperature, which does not sh

29 It has been found that above 1 GPa the photoreaction becomes inhibited.

30 nly organic reaction product observed in the photoreaction between (1R,2S,5R)-menthyl chloride and me

31 An efficient and environmentally friendly photoreaction between phenyl isocyanate or pentafluoroph

32 Short-range and long-range photoreactions between ethidium and DNA have been charac

33 tizer moiety, does not undergo any secondary photoreactions but selectively yields only triplet alkyl

34 The k(obs) for photoreaction by 20 microM AMPS-Succ-BP is decreased 10-

35 orientation and within a viable distance for photoreaction by electronically complementary interactio

36 The modulation of SRII photoreactions by HtrII indicates that SRII and HtrII ar

37 the primary magnetic field effect on flavin photoreactions can be amplified chemically by slow radic

38 Photoreaction caused SWCNTs to lose oxygen-containing fu

39 es as both the binding pharmacophore and the photoreaction center for this molecule.

40 ocks for assembly of the first O(2) evolving photoreaction center, most likely originating from green

41 New crystallographic data for the bacterial photoreaction centre have brought an intriguing insight

42 Nase P holoenzymes form specific products in photoreactions containing [4-thio]-uridine-labeled pre-t

43 two types proteorhodopsin during the initial photoreaction despite their similar chromophore structur

44 veral differences in the BPR and GPR primary photoreactions despite the similar structure of the reti

45 way to control the stereochemical course of photoreaction due to the orbital approaches required for

46 In contrast to aqu/nC60, the photoreaction efficiencies of the hydrophilic fullerene,

47 tive oxygen species via a complex process of photoreactions, ending up in photobleaching, the mechani

48 ed by a PBG that must undergo two sequential photoreactions for each molecule of base generated.

49 This new photoreaction has also been tested in the production of

50 nt of ethoxy and phosphinoyl radicals in the photoreaction has unequivocally been evidenced by EPR sp

51 capable of undergoing type II and/or type I photoreactions has been explored in isotropic solution a

52 e pairs closer to the orientation needed for photoreaction have higher crosslinking frequencies.

53 The quantum yields of the photoreactions have been determined with the N-(phenyl)f

54 The observed intramolecular photoreactions have proven to be a straightforward entry

55 energy photons for the primary and secondary photoreactions; (iii) it enhances the quantum yield of i

56 ne the structural changes during the primary photoreaction in blue-absorbing proteorhodopsin (BPR), a

57 We studied the back-photoreaction in both native SRI and its transducer free

58 as synthesized from a gemini monomer through photoreaction in the solid state.

59 The photoreactions in cyclopentane, 2-methyl-2-propanol, and

60 Comparative studies of the same photoreactions in micellar media demonstrate that dendri

61 Comparative studies of the same photoreactions in micelles formed from small molecule su

62 ns and kinetic parameters for the sensitized photoreactions increased as the spectral slope coefficie

63 The quantum yields of these photoreactions increased when electron-withdrawing group

64 Using photoreaction injection molding in poly(dimethylsiloxane

65 Using photoreaction injection molding, we were also able to ge

66 Our results suggest that the initial photoreaction involved in phytochrome conversion is rela

67 avoiding microscopic reversibility since the photoreaction involves an electronically excited state.

68 e SWCNTs is generally low; however, indirect photoreaction involving .OH may be significant in natura

69 erocyanine takes 1.6 ps whereas the reversed photoreaction is accomplished within 25 ps.

70 ime of the room-temperature rhodopsin (RhRT) photoreaction is measured for the first time using picos

71 It is probable that the primary photoreaction is mechanistically analogous to pyrimidine

72 Although the photoreaction itself is now well-characterized experimen

73 fects of natural organic matter (NOM) on the photoreaction kinetics of fullerenes (i.e., C60 and full

74 e analyzed within the framework of rhodopsin photoreaction kinetics.

75 Prototypical photoreactions, namely, photo-Fries reaction of (a) 1-na

76 is photoactive and enables an unprecedented photoreaction not observed in bulk solution.

77 Analogous photoreaction occurs with the O-tert-butyl ester (t)BuDT

78 ecular competition reactions were studied by photoreaction of 1 in C6F6 with benzene and another subs

79 et excited acetophenone, the main sensitized photoreaction of 7Z in benzene being deoxygenation.

80 Quenching constants for the photoreaction of aqu/nC60 correlated approximately with

81 M from several sources quenched (slowed) the photoreaction of C60 aggregates in water (aqu/nC60), but

82 Photoreaction of diazo Meldrum's acid (1) shows a unique

83 ter (aqu/nC60), but sensitized (accelerated) photoreaction of fullerenol.

84 es show that the rate of the initially rapid photoreaction of GO is insensitive to the dissolved oxyg

85 Photoreaction of methyl 4-O-azidocarbonyl-2,3,6-trideoxy

86 tal structures of three intermediates in the photoreaction of Pseudomonas aeruginosa bacteriophytochr

87 roducts of retro-1,3-dipolar addition during photoreaction of starting pyrazol-4-one is directly conf

88 These results indicated that photoreaction of the amorphous carbon was likely involve

89 The photoreaction of the bis-SorbPC-containing LUV yields cr

90 Here, we investigated the photoreaction of the PHR by time-resolved step-scan FT-I

91 kinetics, spectroscopy, and mechanism of the photoreaction of this molecule and its photoinduced inte

92 Photoreactions of 4-nitroanisole and the 2-halo-4-nitroa

93 However, comparison between the photoreactions of 9 and 11 does not show similar structu

94 The products of photoreactions of conjugated organic molecules may be al

95 tryptophan triad does not necessarily alter photoreactions of cryptochromes in vivo.

96 The photoreactions of halorhodopsin are complicated by the f

97 The results of this effort show that (1) photoreactions of N-trimethylsilylmethyl-substituted alp

98 The photoreactions of the Pr ground state of cyanobacterial

99 We studied the aqueous photoreactions of three phenols (phenol, guaiacol, and s

100 Photoreactions of trans-3,5-dihydro-3,5-dimethyl-3,5-dip

101 In these photoreactions oligomer I(A) appears to selectively form

102 erms of the molecular rearrangement during a photoreaction or a photophysical event is one of the mos

103 of a crown ether moiety allows changing the photoreaction parameters by means of complexation with M

104 magnetic compass; however, the cryptochrome photoreaction pathway is not fully resolved yet.

105 at protonation of acidic group(s) alters the photoreaction pathway that leads normally to all-trans -

106 our findings on A. thaliana cryptochrome to photoreaction pathways in animal cryptochromes.

107 iven dynamic response that is common to both photoreaction pathways.

108 e reaction partners for this three-component photoreaction (Porta-type process) which also provides a

109 ctural changes that occur during the primary photoreaction (PR --> K) of wild-type pigment and two mu

110 ges by scanning the temperature at which the photoreaction proceeded.

111 ve the same crystal orientation and that the photoreaction proceeds in a crystal-to-crystal manner.

112 In the present work, the resveratrol photoreaction products were analyzed by HPLC, and one of

113 The photoreaction quantum yield of rhodopsin is wavelength d

114 nd that Au particle size does not affect the photoreaction rate over the 3-12 nm range.

115 Only one intermediate of this back-photoreaction, S(b)(510), is known.

116 Thus, in any photoreaction scheme at least four species have to be ac

117 ein, we describe a picomole-scale, real-time photoreaction screening platform in which a handheld las

118 ic channel both upfield and downfield from a photoreaction site formed by high-numerical-aperture opt

119 The porphyrin cation photoreaction specifically modifies G18, G20, and G34 in

120 The isoxazole photoreaction starts to occur upon irradiation at lambda

121 emical and quantum yields observed for these photoreactions suggests that these esters can be used as

122 In this report we describe a porphyrin ion photoreaction that enables one to monitor RNA stacking i

123 socyanates, are produced in good yields in a photoreaction that is apparently governed by the acidic

124 ction is not part of the insect cryptochrome photoreaction that results in proteolytic degradation of

125 that Tlr0924 undergoes an unprecedented long photoreaction that spans from picoseconds to seconds.

126 By exhaustive search analysis, two photoreaction time constants of (4.7 +/- 1.4) and (30 +/

127 s an alternative fragmentation-translocation photoreaction to afford angular tricycle 6.

128 Based on comparison of SRII photoreactions to those of sensory rhodopsin I and bacte

129 n of Avena sativa, both before and after the photoreaction, to answer this question.

130 e removal of amorphous carbon after indirect photoreaction was confirmed with thermogravimetric analy

131 Each photoreaction was cytocompatible and tunable, rendering

132 on the forward (dark- to light-adapted form) photoreaction was observed, the change in Y21 pKa led to

133 d and taken up in each step of the rhodopsin photoreaction, we concluded that two forms of Meta-II ar

134 Photoreactions were carried out at low temperature in th

135 These photoreactions were efficient under inert atmosphere and

136 rface waters (direct photolysis and indirect photoreactions) were studied for EMIM, to assess its per

137 intermediates before the second step of the photoreaction where the reaction pathways diverge, the l

138 The photoreaction, which occurs by release of bromine radica

139 e directly in functioning mitochondria after photoreaction with a rhodium intercalator that penetrate

140 amage to authentic mitochondrial DNA through photoreactions with a rhodium intercalator.

141 them from quantum yield measurements for the photoreactions with CCl(4) (a metal-radical trap) as a f

142 precession and thus recombination rates and photoreaction yields, giving rise to a range of magneto-