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1 attributed to isomerism of the methoxy-based chelates.
2 IRT) in addition to Fe(III)-phytosiderophore chelates.
3  macrocyclic GBCA chelates in lieu of linear chelates.
4 ept for such in vivo evaluation, here of the chelates (52)Mn-DOTA and (64)Cu-DOTA.
5 ate (DDC), a strong (64)Cu ligand, which can chelate (64)CuCl2 from the following injection to form t
6  active site, Asn211 is observed to directly chelate a hydrated divalent metal ion and Arg124, on the
7 central channel of the trimeric Dut where it chelates a divalent ion.
8 ation of the highly conserved Gln-758, which chelates a nucleotide-associated Mg(2+) ion, eliminated
9 lgranulin B oligomer, MRP-8/MRP-14 oligomer) chelates a number of first-row transition metals, includ
10                                    The metal chelating abilities (34.92-57.38mgEDTA/g) and in vitro a
11 ical scavenging, reduction of metal ions and chelating abilities against ferrous ions.
12 ) radical scavenging activities, ferrous ion chelating abilities and reducing power results showed th
13              All these polyanils showed good chelating abilities toward trivalent boron fragments suc
14 al scavenging capacity (50.18-86.79%), metal chelating ability (0.21-8.15%), ferric ion reducing powe
15  assay (67.66%), ABTS assay (78.81%), Fe(2+) chelating ability (51.20%), hydroxyl assay (60.95%) and
16 ical, ABTS radical, hydroxyl radical, Fe(2+) chelating ability and reducing power.
17 ty measurements, i.e. the reducing power and chelating ability measurements, for appropriate comparis
18                                       Cu(2+)-chelating ability was significantly correlated to FRAP,
19 0.05) correlations were obtained with Fe(2+)-chelating ability.
20 ckness, and the results demonstrate that the chelating action and dispersing effect of EDTA is critic
21 ylhydrazyl radical inhibiting and Fe(2+) ion chelating activities (IC50 25.05 and 350.7muM, respectiv
22 radical scavenging, reducing ferric ions and chelating activities.
23 ing activities (p<0.05), but limited ferrous chelating activities.
24 hing inhibition (91.75 +/- 0.22%) and Cu(2+)-chelating activity (74.53 +/- 0.58%).
25  activity (IC50=39.33 +/- 3.2 mug/mL), metal chelating activity (IC50=56.51 +/- 3.6 mug/mL) and inhib
26 were analyzed for antioxidant activity, Iron chelating activity and total phenolic content.
27         In contrast, reducing power and iron chelating activity seemed to be caused by peptides.
28 s showed significantly (p 0.05) higher metal chelating activity than other fractions.
29 hocyanin content and 16.6-43.2% higher metal chelating activity than the cultivars grown in plains (9
30         All sub-fractions showed high Fe(2+) chelating activity.
31 scavenging activity, reducing power and iron chelating activity.
32 assay showed 71.3% inhibition and 65.8% Iron chelating activity.
33 eds are good source of antioxidants and Iron chelating activity.
34                 WF possessed moderate copper chelating activity.
35                                   Gadolinium chelate administration is not necessary for accurate dia
36 other electrochemical sensors based on metal-chelate affinity complexes.
37       Mononickel catalysts bearing related N chelates afford comparatively low cyclopropane yields (<
38            Treating infant formulas with the chelating agent diethylene triamine pentaacetic acid (DT
39  been developed using the incorporation of a chelating agent in a common organic solvent, dimethyl su
40 or precursor cadmium complex that works as a chelating agent in order to increase optical and electri
41  suggests the importance of the alkali metal chelating agent in the reversibility of dinitrogen bindi
42 uman growth hormone, rhGH) modified with the chelating agent S-2-(4-isothiocyanatobenzyl)-1,4,7-triaz
43               Furthermore, the amount of the chelating agent used also affects the phase purity and e
44 stability increased to a great extent when a chelating agent was added.
45 ma mandarin fruits was extracted to obtain a chelating agent-soluble pectin fraction (ChSS), a dilute
46 e, a target interaction element, and a metal chelating agent.
47  with deferoxamine, a clinically useful iron-chelating agent.
48                                              Chelating agents (EDTA formulations) reduced E. coli CFU
49 ubstantially surpassing conventional Gd(III) chelating agents (r1 approximately 3 mM(-1)s(-1) at 4.7
50 ical "braking" system was achieved by adding chelating agents capable of sequestering the metal ion e
51                      Treatment of DHHC3 with chelating agents in vitro replicated both the specific s
52  this system being less influenced by pH and chelating agents present in the extracts.
53                                   Currently, chelating agents used in (68)Ga radiopharmaceuticals do
54  to the disease itself, iron overload or the chelating agents used.
55                        Rather than using the chelating agents which are commonly used in CPE to form
56  application of UV-Fenton processes with two chelating agents, nitrilotriacetic acid (NTA) and [S,S]-
57 ic acid, citrate, into the soil rhizosphere, chelating Al(3+) ions and thereby imparting Al-resistanc
58 re in rapid equilibrium with ethylene-opened chelates, (alpha-diimine)Ni(R)(C2H4)(+) complexes, the s
59 s how the new and rapidly expanding class of chelating ancillary ligands bearing 2,2'-bipyridyl, 1,10
60     Most bacteria have evolved mechanisms to chelate and transport ferric iron (Fe(3+)) via sideropho
61 nslocation velocities across a Cu(2+) HisTag-chelated and collagen-bound A1 single domain and A1A2A3
62 R contrast agents that contain three Gd(III) chelates and an IR-783 dye moiety.
63  To synthesize two low-molecular-weight iron chelates and compare their T1 contrast effects with thos
64 interactions of multiple unstable lanthanide chelates and nonantenna ligands with sample leading to a
65 C sensitization was only observed from metal-chelates and QDs.
66 interactions of multiple unstable lanthanide chelates and selected chemicals within the sample leadin
67  donor classes including organic dyes, metal chelates and semiconductor quantum dots (QDs).
68                                              Chelating and free radicals scavenging activities of ext
69 ers using three model systems (DPPH, ferrous chelating and reducing power).
70                                     Both the chelating and the indicating nanospheres showed good sel
71 ting the rearrangement via a lithium enolate chelate, and (3) imparting its influence on consecutive
72 ate that holomycin is an intracellular metal-chelating antibiotic that inhibits a subset of metalloen
73  6-pyrazolyl-2-phenoxylpyridine chromophoric chelate are synthesized.
74                                        These chelates are rapidly opened with ethylene forming alkyl
75                                         Such chelates are the major catalyst resting states but are i
76 e installation of other donors as the fourth chelating arm, while avoiding the formation of stereoiso
77 g a new class of planar tetradentate Mn(III) chelates assembled from a 1,2-phenylenediamido (PDA) bac
78 ntial for antimalarial activity supporting a chelate-based quinone methide mechanism involving metal
79 f photophysical titrations show this Eu(III) chelate behaves as an "on-off" luminescent switching pro
80         These styrenes are precursors to the chelating benzylidene moiety in a proposed series of nov
81 yclobutadiene complex through a multidentate chelate binding mode.
82 most preferred route begins with a bidentate chelate binding of deprotonated substrate to the Ni.
83                                    The first chelating bis(N-heterocyclic silylene)xanthene ligand [S
84 I) metal complexes possessing two tridentate chelates (bis-tridentate) are known to be more robust co
85  been prepared from carboxylate ions and the chelating/bridging ligand alpha-methyl-2-pyridine-methan
86  into strands through silver ions, which are chelated by the amine functions of one open cage and bou
87 ctahedral ammine complexes that are kappa(2)-chelated by the conjugate base.
88                                      When we chelated Ca(2+) ions and raised the pH, we observed a gr
89                           In live zebrafish, chelating calcium after the first wave, but before the s
90                     In cultured DRG neurons, chelating calcium early in the process of WD did not alt
91 rocess of WD did not alter degeneration, but chelating calcium late in WD delayed fragmentation.
92 system resulted in high levels of dispersed "chelated" calcium; conversely, disodium phosphate additi
93 n spectroscopy (AAS) was used to verify iron chelating capability of nanogels.
94 tal complex stability, we evaluated the zinc-chelating capacity and stability of zinc complexes of wh
95  pectin (>/=58%), probably due to its higher chelating capacity of pro-oxidative metal ions (Fe(2+)),
96 c-binding amino acids but showed higher zinc-chelating capacity than WPH-Pap.
97 and peroxyl radicals, the reducing power and chelating capacity were, in general, in the decreasing o
98 d in Escherichia coli and purified by Nichel-chelating chromatography.
99 als of Y. luopingensis indicates that simple chelate claspers in males are plesiomorphic for horsesho
100 0 000 administrations compared with the same chelate classification without protein binding, at 5.2 (
101 he two chiral twisted-boat conformers of the chelated COD included in the already chiral cavity of th
102  the two cyclochiral conformers of the Ir(I) chelated COD was 5 kcal mol(-1) higher as an included or
103  stereoinduction by a well-defined metal O,O-chelate complex of the 3-acyltetramic acid moiety.
104 s they facilitate a mononuclear six-membered chelate complex via the displacement of two hydroxo/aquo
105  method is based on the formation of anionic chelate complexes of Al(III) and Cr(VI) with o-hydroxy a
106 wed a significant decrease in the gadolinium chelate concentration in amniotic fluid compared with th
107 ted imaging; and-before and after gadolinium chelate contrast enhancement-T1-weighted 3-dimensional s
108 pieces were connected via a highly efficient chelate-controlled addition of a vinyl zincate to an alp
109  (allosteric) cooperativity, intramolecular (chelate) cooperativity and interannular cooperativity an
110 ted within the macrocycle cavity are able to chelate copper(I) endotopically.
111                                DPM-1001 also chelates copper, which enhanced its potency as a PTP1B i
112   This system is evaluated in batch mode via chelating copper at the active site of tyrosinase and in
113 f detection: 0.019microM and 0.008microM for chelating copper at the active site of tyrosinase and th
114 onverting enzyme inhibitor that operates via chelating copper at the active site of tyrosinase and th
115 ,6-iPr2C6H3)}2](n) (n = 0 to -4), (dadi)(n), chelates Cr and Fe to give [(dadi)M] ([1Cr(thf)] and [1F
116                                          Mbn chelates Cu with high affinity, and the Cu-loaded form (
117 leptic complexes of the Fe(II) d(6) ion with chelating diimine ligands.
118 3))-H activation, including requirements for chelating directing groups and high reaction temperature
119 of non-exchangeable protons from macrocyclic chelates (e.g., DOTP(8-)) complexed with paramagnetic th
120 rmed in solution, by taking advantage of the chelate effect.
121 ooperative inductive, mesomeric, steric, and chelate effects are discussed.
122             (18)F-FDG avidity and gadolinium chelate enhancement were concordant in 30 of the 36 pati
123 nce between (18)F-FDG avidity and gadolinium chelate enhancement.
124 stable than the internally hydrogen-bonded ("chelated enol") conformer (CE).
125                               The hemilabile chelate facilitates conversion of a principally ligand-b
126 erimental protocols to assess the ability to chelate Fe(2+) and Cu(2+) using 96-well microplates, we
127 ssess the ability of plant-based extracts to chelate Fe(2+) and Cu(2+)in vitro.
128 e further show that ICDH-Coumarin is able to chelate Fe(3+) to switch off RssAB signaling, triggering
129 ulate matter such as biomass burning aerosol chelate Fe(II), but the effect on ROS formation in the p
130 sults suggest that siderophores could partly chelate Fe(III) in cloud waters and thus potentially imp
131 n combination with a colorimetric screen for chelated Fe(III)-NTA reduction with NADH as electron don
132 te the PSMA ligand MIP1404, which contains a chelate for (99m)Tc/rhenium.
133 e starting to question the use of gadolinium chelates for clinical magnetic resonance (MR) imaging.
134                                              Chelate formation and coordination of the Ni center to t
135  propose that the active reductant is an N,O chelate formed between SmI2 and 2 equiv of TEU(-).
136     These materials can degrade into smaller chelating fragments at rates proportional to the level o
137 ochemistry from classic approaches to modern chelate-free or intrinsic methods.
138 allenge have generated a range of innovative chelate-free radiolabeling methods that exploit intrinsi
139  TdTs facilitate utilization of iron or iron chelates from host-derived proteins, including transferr
140  phyla of the tested strains and the type of chelating functional groups (i.e., hydroxamate, catechol
141                          The nonionic linear chelate gadodiamide had the lowest rate of reactions, at
142 on in a hexadentate fashion using a new iron-chelating gamma-amino acid.
143 al labelled with SPIONs and gadolinium-based chelates (GdDTPA).
144 t herein a novel allysine-binding gadolinium chelate (GdOA), that can non-invasively detect and quant
145 erately higher concentrations, however, iron chelates generated similar contrast effects at T1-weight
146    Radiotracer design modifications included chelate, glycosylation, and radiometal.
147  extrapolated to substrates bearing a single chelating group, providing further insight into the reac
148        Hydroxamic acids are outstanding zinc chelating groups that can be used to design potent and s
149 s as ligands that combine two distinct metal-chelating groups, lipoic acid and imidazole, for the sur
150 lution, but evidence of a stable oxidized Bk chelate has so far remained elusive.
151                                        Metal-chelating heteroaryl small molecules have found widespre
152                               The Gadolinium-chelated HPMA copolymers also showed significant enhance
153                                      The two chelating IL systems (one with a pendent polyether chain
154                        Amounts of gadolinium chelate in the fetal tissues and amniotic fluid were min
155  time points, the distribution of gadolinium chelate in the fetus was comparable to that expected in
156 ntrations of multiple linear and macrocyclic chelates in a rat model to better understand the scope a
157 sequences of the bite angle of five-membered chelates in cubic tetramers and resulting solvation numb
158 following administration of macrocyclic GBCA chelates in lieu of linear chelates.
159 and the color evolution of anthocyanin-metal chelates in pH 3-8.
160 xpression and stability of Al(3+) and Fe(3+) chelates in pH 6-7 were evaluated by spectrophotometry (
161 demonstrating that the pharmacophores of the chelating inhibitors (S)-10a, (R)-10a, and 10b were bind
162 ult in formation of observable five-membered chelate intermediates.
163  the auxiliary, with the metal cation (K(+)) chelated into the malonate six-membered hole as a Z-enol
164 actin (MBT) and carboxymycobactin (cMBT), to chelate intracellular iron.
165     Molecular analysis revealed that Ent can chelate intracellular labile iron that is required for n
166                                              Chelating ionic liquids (ILs), in which polyether chains
167                                     EDTA can chelate iron and lead.
168 tor, deferiprone, is well tolerated, able to chelate iron from various brain regions and improve PD s
169 ly compromised the ability of transferrin to chelate iron, as iron chelation combined with sodium bic
170 l polyphenol content and their capacities to chelate iron.
171 er than deferasirox, but rapidly donates the chelated iron to deferasirox, consistent with a shuttlin
172 perturb the electronic properties of the SAM-chelated iron-sulfur cluster.
173 actors linked to AD pathogenesis, namely by: chelating iron, copper and zinc; scavenging reactive oxy
174 valuate whether administration of gadolinium chelates is necessary for evaluation of pediatric tumors
175          The in vivo stability of radiometal chelates is widely debated but studies that mimic a real
176 nied by conformational changes in the Ni(II) chelate itself.
177 its two terminal aryls to afford a bidentate chelating ligand (CN(tBu)Ar3NC) that is able to stabiliz
178 o-Vanillidine-2-amino-p-cresol was used as a chelating ligand and 1-undecanol was selected as an extr
179 onalization based on judicious choice of N,O-chelating ligand and metal center.
180  of the phenyl ring of 2-phenylbenzimidazole chelating ligand of the ruthenium (3a-g) and iridium com
181 anism for homogeneous catalysts in which the chelating ligand plays a key role in facilitating the ca
182                                Addition of a chelating ligand that complexes free silver ions indicat
183 lvent, extraction time, concentration of the chelating ligand, salt effect, centrifugation time and s
184 rifluoromethylation of unprotected bidentate chelating ligand, xanthine alkaloids, nucleosides, and r
185 n fluorophores with heterobiaryl N,O- or N,N-chelate ligands were prepared and photophysically charac
186                                      1,3-N,O-Chelating ligands are ubiquitous in nature owing to thei
187                          A series of new P^P-chelating ligands constituted by a dicationic -[P(H2Im)2
188                                   Due to its chelating ligands, Cr(CN(tBu)Ar3NC)3 is more robust than
189 adding clustering agents, such as calcium or chelating ligands, favor the lateral cis adhesion of the
190 noline), O,O (diketonate), or S,S (dithione) chelating ligands, have been characterized by X-ray crys
191 dened spectra seen with enzymes and strongly chelating ligands.
192 , bears a long stout uniramous antenna and a chelate limb followed by two biramous appendages.
193 proton relaxitivities compared with other Gd-chelates, making them the promising contrast agents for
194                 cbl1 plants exudated less Al-chelating malate, accumulated more Al, and displayed a s
195 titution generally increased lambdamax of Cy chelates: malonic acid monoacylation<triglycosylated Cy<
196          While DPA displayed a propensity to chelate metal ions from NDM-1, 36 formed a stable NDM-1:
197 ns of the phosphonate group of the alpha-CNP chelate Mg(2+), mimicking the chelation by the beta- and
198  the CR3 I domain by direct contact with the chelated Mg(2+) ion.
199 nd synthesis of potent but nonselective zinc-chelating MMP inhibitors (e.g., 10a and 10b).
200                                           PP chelates Mn(III) produced by the enzyme and subsequently
201 extrin (beta-CD) and ferrocene (Fc) and iron chelating moieties composed of deferoxamine (DFO) into t
202     This work expands the repertoire of iron-chelating moieties in microbial siderophores.
203 ll-L-serine- (MAS3) and all-D-serine- (mas3) chelating moieties were evaluated in parallel, and a kit
204                                   Small iron-chelating molecules called siderophores were selected as
205  and 7 display rather high basicity, forming chelated monocations.
206 wo contrast agents: a clinically approved Gd chelate, Multihance((R)) (gadobenate dimeglumine), and a
207  of both Evans blue dye (EBD) and Gadolinium-chelated N-(2-hydroxypropyl)methacrylamide (HPMA) copoly
208 ll, renal clearable, silica based gadolinium chelated nanoparticles (SiGdNP) provide simultaneous MR
209 iotics and emphasizes the potential of metal-chelating natural products in antimicrobial therapy.
210                                    The metal-chelating noncanonical amino acid (2,2'-bipyridin-5yl)al
211 A-modified somatropins as well as to gallium chelated NOTA-functionalities (Ga-10:1 NOTA-somatropin);
212           Two previously described iron (Fe) chelates of pentetic acid (Fe-DTPA) and of trans-cyclohe
213 ypically rely on using traditional metal ion chelate or prosthetic group chemistries.
214 ants, such as betaine and polyols, and metal-chelating organic acids.
215              Besides, the detection of metal-chelating peptide is not sensitive enough by spectrophot
216 set up an original method of screening metal chelating peptides in a hydrolysate using Surface Plasmo
217                    For the first time, metal chelating peptides were screened in hydrolysates using S
218 t efficacy to selectively separate the metal-chelating peptides.
219 operation between iridium(III) and a 1,3-N,O-chelating phosphoramidate ligand has been used to develo
220 tage of time-resolved luminescence of Tb(3+)-chelated phosphotyrosine-containing peptides, which faci
221 s accomplished by using the metallic-complex chelating polymer Mix&Go.
222 ging activity, higher on green tea, and iron chelating potential, higher on L. algarvense.
223 ce; however, only the aspartic acid modified chelates produced an amide proton-based PARACEST signal.
224  strategy that enables to modulate the metal chelating properties of hydroxamic acid groups by bioort
225  activity in terms of radical scavenging and chelating properties.
226 ducing ferric ions and showed the best metal chelating properties.
227 athway with metabolic intermediates of metal-chelating properties.
228 s effect is fully related to its potent iron-chelating property in the organelle.
229  biological coordination chemistry of Ni(II)-chelating proteins in nature and provide a foundation fo
230                         Additionally, Cu(II) chelated PyED outcompetes DNA polymerase I to successful
231 ariety of strategies were explored to form a chelated radical intermediate en route to xiamycin A, in
232  (2H7), with the other arm of the FP an anti-chelated radiometal trap for a radiolabeled ligand (yttr
233 using 1-(2-Pyridylazo)-2-naphthol (PAN) as a chelating reagent and detection by electrothermal atomic
234 s using 2-thenoyltrifluoroacetone (TTA) as a chelating reagent by ETAAS.
235 rom the conjugate, in the presence of strong chelating reagent ethanedithiol.
236 rstly synthesized and characterized as a new chelating reagent for determination of some metals.
237          Diethyl dithiocarbamate was used as chelating reagent.
238 ice were incubated with excess Cu or with Cu-chelating reagents; effects on cell fat content and ATP7
239                                              Chelate rearrangement via beta-silyl elimination account
240 y leading to low chlorophyll but high ferric-chelate reductase activity and coumarin release.
241 of FRO2 transcript levels, as well as ferric chelate reductase activity, and is causal for a portion
242 d by an impaired ability to boost the ferric chelate reductase activity, which is an essential proces
243 through the analysis of expression of ferric chelate reductase, iron-regulated transporter, and putat
244 ed in iron-regulated transporter1 and ferric chelate reductase2 knockout mutants and was prioritized
245  higher reduction potential than most Eu(II) chelates reported to date.
246 ycidyl methacrylate (GMA) based terpolymeric chelating resin was synthesized for the separation and p
247                                         This chelating resin was used as a new adsorbent material for
248 , volume of the sample and eluent, amount of chelating resin, and interference of ions were examined.
249                                        A new chelating resin, poly [2-(4-methoxyphenylamino)-2-oxoeth
250                                        A new chelating resin, poly(N-cyclohexylacrylamide-co-divinylb
251 s and then boiled in the presence of a metal chelating resin.
252 nsertion pathways to yield 4- and 5-membered chelates, respectively.
253 conformers associated with the five membered chelate rings (lambda/delta), alignment modes of the C-C
254 ociated with each particular topology of the chelate rings formed.
255                                      Neither chelating salt produced high levels of soluble protein.
256 m citrate either alone or as part of a mixed chelating salt system resulted in high levels of dispers
257 pite its simplicity, was a good indicator of chelating salt-calcium interactions in rennet casein dis
258 tudy elucidates the critical role of calcium chelating salts in modulating casein hydration and dispe
259                                 Thus calcium chelating salts may play a more subtle role in modulatin
260 is study investigated the effects of calcium chelating salts on calcium-ion activity (ACa(++)), calci
261                    In the absence of calcium chelating salts, these concentrations were significantly
262 reased with increasing concentration of both chelating salts.
263 antly higher for matrices containing calcium chelating salts.
264 ferent in the presence or absence of calcium chelating salts.
265 nufacture of the matrices containing calcium chelating salts; with approximately 23% of total calcium
266 or each type of oxygen-donor present in such chelating (Section 1) or bridging (Section 2) hybrid lig
267 e structure of xanthan, which generates more chelating sites at pH 3.5 than at pH 5.5.
268 st-effective material with a high density of chelating sites designed for mercury capture and therefo
269 ude hierarchical porosity, a high density of chelating sites, and the material's robustness, which im
270  only those proton donors that coordinate or chelate strongly to Sm(II) promote anthracene reduction
271 he feasibility of highly selective non-metal chelating, substrate-competitive inhibitors of the JmjC
272 antitatively displace DMEA, affording doubly chelated symmetric dimers.
273 lent attachment of a paramagnetic lanthanoid chelating tag to the ligand of interest.
274 coiled-coil peptides bearing unnatural metal-chelating terpyridine moieties.
275  (oxygen nanosensors) and a pH sensitive BF2-chelated tetraarylazadipyrromethene dye (aza-BODIPY) was
276 nsing materials are based on fluorescent BF2-chelated tetraarylazadipyrromethene dyes (aza-BODIPYs) d
277 xiliary [4Fe-4S] cluster of HydG and further chelates the dangler Fe.
278 he aryl chromophore and the appended arsenic chelate: the fluorescence is rotamer-restricted.
279 cal trials evaluating the usefulness of iron-chelating therapy in critical illness and sepsis.
280 emokine with CXCR1 (1-350) containing Mn(2+) chelated to an unnatural amino acid assists in the chara
281  in which imine acts as a directing group by chelating to the metal center, affords a potential route
282  the catalytically active Zn(2+) ion without chelating to the metal.
283 obust compared to those with three bidentate chelates (tris-bidentate).
284 very generally entails chemotypes capable of chelating two divalent metal ions in the RNase H active
285                                   The diaryl chelate unit has a significant impact on J-aggregates an
286                  Spiro-BODIPYs with a diaryl chelate unit have been found to form J-aggregates in met
287 on the length of linker connecting the metal chelating unit to the hydroxyl group.
288 ng within the MMP-13 active site, the Zn(2+) chelating unit was replaced with nonchelating polar resi
289 contrast agent with a single gadolinium (Gd) chelate using a quantitative MRI T1 mapping technique in
290 re used as donors, and a luminescent Eu(III)-chelate was used as an acceptor.
291          The dynamic contrast effects of the chelates were compared by performing DCE MR imaging with
292           The T1 contrast effects of the two chelates were compared with those of gadopentetate dimeg
293 dified to form a bifunctional chelator and 4 chelates were conjugated to a fibrin-specific peptide to
294 cts of hydroxycinnamic acids on cyanidin and chelates were investigated by addition of the acids to t
295 ls, readily participates in the formation of chelates when embedded into such a scaffold.
296  H2 binding enthalpy of 5 linkers which were chelated with 11 different transition metals (Tm), inclu
297 C inhibitors contain hydroxamate moiety that chelates with zinc ion to become the cofactor of HDAC en
298 activity primarily because of its ability to chelate zinc and manganese.
299 reductively activated, and reduced holomycin chelates zinc with high affinity.
300 rotein that exerts antimicrobial activity by chelating zinc and manganese.

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