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1  AFs accumulation in stored maize, replacing synthetic compounds.
2 , validated, and used to screen a library of synthetic compounds.
3 ably with experimental results found for the synthetic compounds.
4 on in response to a diversity of natural and synthetic compounds.
5  metabolites, signaling molecules, and other synthetic compounds.
6 have been reported of SF-1 in complexes with synthetic compounds.
7 ntibiotic drugs and even diverse natural and synthetic compounds.
8 herry-picked from all commercially available synthetic compounds.
9 ne the allosteric regulation of myosins with synthetic compounds.
10 fied by screening our in-house collection of synthetic compounds.
11 ermine the absolution configurations of such synthetic compounds.
12 resent in a broad range of other natural and synthetic compounds.
13  of the substrates used to assay cytGSTs are synthetic compounds.
14 ely used building blocks in both natural and synthetic compounds.
15 , mandelalides E-L (5-12), and the supply of synthetic compounds 1 and 12, as well as seco-mandelalid
16 thocholic acid, oleanolic acid [OA], and two synthetic compounds), (2) a novel TGR5 antagonist (m-tol
17                           Here we describe a synthetic compound, 2-fluoro-1-methoxy-4-pentafluorophen
18 ram around an identified hit resulted in new synthetic compound 26 [UCM-1306, 2-(fluoromethoxy)-4'-(S
19                       We report that EF24, a synthetic compound 3,5-bis(2-flurobenzylidene)piperidin-
20                               By contrast, a synthetic compound, 3-(1H-imidazol-1-ylmethyl)-2phenyl-1
21 y for new anticancer agents and identified a synthetic compound, 5-(2,4-dihydroxybenzylidene)-2-(phen
22 te MAIT cells but compete with bacterial and synthetic compounds activating MAIT cells, providing the
23 rived natural product, ikarugamycin; and the synthetic compound, alexidine dihydrochloride, which is
24                        Retinoic acid and its synthetic compound AM80 play roles in immunoregulation b
25 s) of the various cytokines showed that each synthetic compound and E. coli 055:B5 LPS induced simila
26 this simple infection system to screen 6,000 synthetic compounds and 1,136 natural product extracts.
27              When placed in field traps, the synthetic compounds and a queen-equivalent mixture rapid
28 harma industry uses, as replacements for the synthetic compounds and also in the valorisation of plan
29  of biologically active natural products and synthetic compounds and can be accessed using mild react
30 he evolution of MGs from natural products to synthetic compounds and discuss integration of emerging
31  particular molecular properties compared to synthetic compounds and drugs.
32        Mouse macrophages were exposed to the synthetic compounds and E. coli 055:B5 LPS, and the resu
33                These modulators include both synthetic compounds and endogenous modulators, such as c
34 date this technique, we prepared mixtures of synthetic compounds and extracts from Arabidopsis thalia
35 and female D. suzukii olfactory responses to synthetic compounds and fruit juices as sources of attra
36                 Biological evaluation of the synthetic compounds and intermediates against a panel of
37 ntiate distributions of natural products and synthetic compounds and is applicable in the analysis of
38 creening of substantially greater numbers of synthetic compounds and natural products, we are not rou
39 were compared with several other natural and synthetic compounds and related to glutathione and ascor
40                    Phthalates are ubiquitous synthetic compounds and therefore difficult to measure i
41                                   SHU9119 (a synthetic compound) and AGRP (an endogenous peptide) are
42 al scaffolds encountered in both natural and synthetic compounds, and their biological activity often
43               The physical properties of the synthetic compound are somewhat different from those rep
44 m this laboratory indicates that a number of synthetic compounds are high affinity transport inhibito
45                  Biomolecules and high-value synthetic compounds are rarely isotropic, highly-symmetr
46  in numerous biologically active natural and synthetic compounds, are efficiently prepared by a Rh(I)
47   In this study, we aimed to develop a small synthetic compound as a UL141 antagonist.
48 re, we examined the ability of TFA-12, a new synthetic compound belonging to tocopherol long-chain fa
49 and designed DNA fragments indicate that the synthetic compounds bind at AT sequences in the minor gr
50       We have shown previously that EM011, a synthetic compound, binds tubulin with a higher affinity
51  the sigma-1 receptor binds a vast number of synthetic compounds but does not bind opioid peptides; i
52                           The replacement of synthetic compounds by essential oils for inhibition of
53 d synthase (FAS) inhibitors (cerulenin and a synthetic compound C75) led to inhibition of feeding and
54  the natural product cerulenin and the novel synthetic compound c75, are selective inhibitors of tumo
55                                However, some synthetic compounds can fall outside the upper boundary
56                       We have found that the synthetic compound CC-5079 potently inhibits cancer cell
57 sense a broad spectrum of ligands, including synthetic compounds, chemokines, mitogens, fatty acids,
58 gineered G-protein coupled receptor with the synthetic compound clozapine-N-oxide (CNO) evoked a shor
59                                        These synthetic compounds contain sequences that are active si
60                                          The synthetic compounds contained pentyl, hexyl, or hexanoyl
61 t a substantial fraction (~20%) of cytotoxic synthetic compounds containing Michael acceptor groups i
62 on of 7 and 8 along with several related key synthetic compounds containing the core residue 4 amidin
63                    Nine structurally related synthetic compounds, containing aromatic or other hydrop
64 d MS/MS fragmentation pattern and, using the synthetic compound, demonstrate that it has bioactivity.
65                             PM534 is a novel synthetic compound derived from the Structure-Activity-R
66                                            A synthetic compound designed to bind in this pocket, and
67                                     ZIP is a synthetic compound designed to inhibit the atypical PKC,
68 ychoactive substances (NPSs) which are small synthetic compounds designed to mimic the effects of oth
69                          The NMR data of the synthetic compound did not conform to the reported natur
70                           In each assay, the synthetic compounds displayed comparable activity to the
71 actions could be efficiently disrupted using synthetic compounds either mimicking or masking this car
72                       A racemic blend of the synthetic compound elicited behavioral and electrophysio
73 mer therefore represents an innovative fully synthetic compound for the treatment of lung inflammator
74 was proposed for use in screening natural or synthetic compounds for cell cycle-dependent (particular
75 ing of a 50000-member library of natural and synthetic compounds for sensitizers of RCC cells to TRAI
76 tionship (QSAR) of a group of endogenous and synthetic compounds for the androgen receptor (AR) using
77 talline materials has prompted the design of synthetic compounds for the regulation of crystal growth
78                            Evaluation of the synthetic compounds for their ability to act as microbe-
79 hroughput whole-cell-based screening of 5000 synthetic compounds from the AnalytiCon NATx library hel
80                     In addition, a number of synthetic compounds have been developed that also target
81          Many categories of both natural and synthetic compounds have been reported to have neuroprot
82                                  A number of synthetic compounds have been shown to block the process
83 way-specific screens of natural products and synthetic compounds have recently provided a number of s
84                                      The new synthetic compounds have two aromatic-amidine groups for
85 ystem for throughput screening of natural or synthetic compounds highly effective on blocking of PRRS
86       We herein report the first examples of synthetic compound-I and activated compound-II species t
87                               Carba-NAD is a synthetic compound identical to NAD except for one subst
88                                          The synthetic compounds identified in these assays should se
89 me may have evolved the ability to hydrolyze synthetic compounds in bacteria under selective pressure
90 the mechanism of stimulation mediated by the synthetic compounds in comparison with natural lipoprote
91  here the efficacies of several of these new synthetic compounds in regulating two types of protein d
92 ar activities remain unexplored, and diverse synthetic compounds including insecticides exert JH-like
93 unctional analyses using highly purified and synthetic compounds indicate that the core structure rec
94 , and further examination revealed that this synthetic compound induced expression of an AP-1 target
95 nrelated small-molecule natural products and synthetic compounds inhibit Sec61 with differential effe
96                                          The synthetic compound ink derived from the dissolution of t
97              Novel AIT preparations, such as synthetic compounds, innovative carrier systems and adju
98 aromatic substances when the amount of added synthetic compound is in tens of percent.
99                         Remediation of these synthetic compounds is difficult and an enormous logisti
100                           A series of chiral synthetic compounds is reported that shows intricate but
101                              SU5416, a novel synthetic compound, is a potent and selective inhibitor
102  PPARs are the targets for the hypolipidemic synthetic compounds known as peroxisome proliferators, a
103 ocessing of compound lesions by human cells, synthetic compound lesions containing UV photoproducts o
104 tration barrier makes screening conventional synthetic compound libraries largely impractical, and ac
105 search for inhibitors in natural product and synthetic compound libraries.
106 ural products for drug discovery in favor of synthetic compound libraries.
107                                        These synthetic compounds made it possible to establish relati
108 gands include a diverse array of natural and synthetic compounds, many of which are toxins.
109                                          The synthetic compounds matched the physical and biological
110                                        These synthetic compounds model peptide-nucleic acid heterocon
111                                          Our synthetic compounds modulated significantly both platele
112                In this report, we describe a synthetic compound of the pyrido[2,3-d]pyrimidine class,
113 oiety found in a large number of natural and synthetic compounds of medicinal significance.
114 l groups comprise a large set of natural and synthetic compounds, often with potent biological activi
115                             These agents are synthetic compounds or natural products and their analog
116  Retinoids are a large family of natural and synthetic compounds related to vitamin A that have pleio
117               A referenced tabulation of the synthetic compounds reported to date is provided.
118                           The degradation of synthetic compounds requires bacteria to recruit and ada
119                                  Analysis of synthetic compounds revealed stereoselectivity of the DA
120 , as well as the use of purified natural and synthetic compounds, showed that this process involved p
121 f the family of flavones and isoflavones and synthetic compounds such as the tyrphostins.
122 , and erysolin) and one of which was a novel synthetic compound termed MARPIN.
123 osophila suzukii to foliage- and fruit-based synthetic compounds tested alone and in association with
124 vated receptor (PPAR) gamma, we identified a synthetic compound that binds to this receptor.
125  or an estradiol-dendrimer conjugate, each a synthetic compound that stimulates kinase-mediated ER ac
126 e-disrupting chemicals (EDCs) are natural or synthetic compounds that are ubiquitous in the environme
127        Perfluoroalkyl substances (PFASs) are synthetic compounds that are widely used in industry and
128  and exciting target for the design of novel synthetic compounds that can act as anti-proliferative a
129            We have identified two classes of synthetic compounds that differentially modulate BAR act
130 s a key skeletal unit in several natural and synthetic compounds that exhibit diverse biological prop
131                       Here we describe novel synthetic compounds that have a unique mode of binding t
132   Lack of efficient access to collections of synthetic compounds that have skeletal diversity is a ke
133  be discovered using a diverse collection of synthetic compounds that have three-dimensional features
134 r screening process was designed to identify synthetic compounds that increase the total amount of fu
135 racterization of transcriptional regulators, synthetic compounds that inhibit transcription, or other
136                       A key feature found in synthetic compounds that is rare in nature is the use of
137 fact, the serum of mice immunized with fully synthetic compounds that mimic cell-surface tumour antig
138                            Xenoestrogens are synthetic compounds that mimic endogenous estrogens by b
139 cidations, and rationally designed bioactive synthetic compounds that were accomplished because of co
140          Amino acid-derived isoindolines are synthetic compounds that were created with the idea of i
141                               The assays use synthetic compounds that were designed to mimic the natu
142 ttention was drawn to certain, predominantly synthetic, compounds that are responsible for disproport
143        Despite the prevalence of fluorine in synthetic compounds, the known biological scope is limit
144 c agents, and it is the first non-polyamide, synthetic compound to specifically recognize a DNA seque
145 interactions involved in the binding of this synthetic compound to the 80S ribosome.
146 he receptor are inferred from the ability of synthetic compounds to affect channel function without i
147  hepatocytes and are among the first totally synthetic compounds to approach the activity of adenopho
148 n difficult, in part due to the tendency for synthetic compounds to bind unpredictably within the lip
149                  The work reported here uses synthetic compounds to evaluate the extent of NN weakeni
150                               Application of synthetic compounds to inhibit potato sprouting is a maj
151 xidants can be used in egg powder instead of synthetic compounds to reduce malonaldehyde production d
152                   The ability of natural and synthetic compounds to stimulate transforming growth fac
153                                         Many synthetic compounds to which we attribute specific activ
154 mimicked reproductive cheaters by applying a synthetic compound typical of fertile individuals on non
155 e methyl siloxanes (VMS) are high-production synthetic compounds, ubiquitously found in the environme
156 h-throughput screen of approximately 200,000 synthetic compounds using Per2lucSV reporter fibroblast
157 natural products, drugs, cosmetics and other synthetic compounds) using a limited number of pre-defin
158                                         Each synthetic compound was reacted under anaerobic condition
159 Proton, (13)C NMR, and molecular mass of the synthetic compound were identical with vesperlysine A, a
160                                          The synthetic compounds were employed to uncover immunodomin
161                                          The synthetic compounds were evaluated for antibacterial act
162                                          The synthetic compounds were evaluated for in vitro antivira
163 a significant portion of biologically active synthetic compounds were found to be pseudo-natural prod
164                                  Indeed, all synthetic compounds were found to bind to the target RNA
165                                          The synthetic compounds were used to examine binding propert
166                            Structures of the synthetic compounds were verified by NMR spectroscopy us
167                        The drug is a totally synthetic compound, which lessens the likelihood of natu
168 ening of a chemical library, we identified a synthetic compound whose inducing ability significantly
169 r- and polyfluoroalkyl substances (PFAS) are synthetic compounds widely employed in society due to th
170                               Imiquimod is a synthetic compound with antitumor properties; a 5% cream
171 this study, we employed virtual screening of synthetic compounds with a natural product scaffold in c
172        Naphthoquinones (NQs) are natural and synthetic compounds with a wide range of biological acti
173  Hence, screening and identifying natural or synthetic compounds with anti-cancer activity via p53-in
174 represent a class of naturally occurring and synthetic compounds with demonstrated antitumor activity
175 f normal reproductive functions, natural and synthetic compounds with estrogen-like activities can fu
176 luoroalkyl substances (PFAS) are over 14 000 synthetic compounds with exceptional environmental persi
177  target and to inform the development of new synthetic compounds with improved potency and reduced cy
178                                       Simple synthetic compounds with only S and C donors offer a lig
179 us antioxidant mechanisms and neutralized by synthetic compounds with peroxynitrite-scavenging capaci
180 occur as constituents of various natural and synthetic compounds with potentially useful bioactivitie
181 f cell migration data for this and two other synthetic compounds with published data on cortistatin A
182     In this case, the evaluation of just six synthetic compounds with seven riboswitch mutants led to
183 th the NMR data and specific rotation of the synthetic compounds with that of the reported data.
184         Furthermore, analyses of four of the synthetic compounds with two important purified resistan
185 of nucleic acid libraries into corresponding synthetic compounds would enable selection and amplifica
186 ion of cytochromes P4501A1/2 (CYP1A1/2) by a synthetic compound YH439 was studied in rodents as well

 
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