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1 stitutes of Health (NIH) Clinical Collection small molecule library.
2 eestatin using a high-throughput screen of a small molecule library.
3 h pocket was identified and screened using a small molecule library.
4 omers through high-throughput screening of a small-molecule library.
5 hat was recently isolated from a DNA-encoded small-molecule library.
6 s platform to screen the 300,000+ member NIH small-molecule library.
7 activity, we screened 114,752 compounds of a small-molecule library.
8 robust and flexible biologically synthesized small-molecule library.
9 ter plates and treated with compounds from a small-molecule library.
10 n, and structure-activity relationships of a small molecules library.
11 y used in drug discovery, using a variety of small molecule libraries.
12 p75NTR was applied to in silico screening of small molecule libraries.
13  of an OBOC combinatorial peptidomimetic and small molecule libraries.
14 s of food contaminants and drug screening of small-molecule libraries.
15 oric model for searching new drug leads from small-molecule libraries.
16 nable direct in vivo phenotypic screening of small-molecule libraries.
17 eactions starting from a large collection of small-molecule libraries.
18  screening of a diverse set of mixture-based small-molecule libraries.
19 s can be identified through the screening of small-molecule libraries.
20 fication of DNA sequences encoding synthetic small-molecule libraries.
21  synthesis of much larger (>10,000-membered) small-molecule libraries.
22 to assess the quality of large DNA-templated small-molecule libraries.
23 ully exploit the power of OBOC combinatorial small molecule libraries, a robust and high throughput e
24 dy serves as a cautionary tale for screening small molecule libraries and provides insights into the
25         Using this model system, we screened small-molecule libraries and identified a compound that
26   We screened RIP1 against GSK's DNA-encoded small-molecule libraries and identified a novel highly p
27 ategy in the construction and selection of a small molecule library, and successfully identified inhi
28  and effectors of biological reactions using small molecule libraries are often hampered by interfere
29                When combinatorial protein or small-molecule libraries are studied, large numbers of b
30 n the combinatorial synthesis of peptide and small-molecule libraries, as catalyst and reagent suppor
31  a cell-based high-throughput screening of a small-molecule library based on TLR3-mediated NF-kappaB
32 h the creation of a natural product-inspired small-molecule library bearing protein-reactive elements
33                              Specifically, a small molecule library biased for binding RNA was probed
34 s identified by virtual screening from a NCI small molecule library, but no data were available about
35  method to screen an epigenetically targeted small molecule library by evaluating regions of aberrant
36 synthesis minimizes the effort to synthesize small-molecule libraries by labelling the molecules rath
37 , two on the RNA and one on the S15 protein, small-molecule libraries can be screened for potential i
38  Ebola proteins with human proteins and with small-molecule libraries, computational modeling of the
39 ry against the entire druggable genome and a small-molecule library consisting of 691,200 compounds u
40 ed by the synthesis and screening of a model small molecule library containing 84 672 member compound
41               We synthesized several focused small-molecule libraries, each composed of a variable ar
42                                  We screened small molecule libraries for compounds inhibiting growth
43                                  We screened small molecule libraries for compounds that directly int
44                         Rational assembly of small molecule libraries for purposes of drug discovery
45 te that cell-based high-content screening of small molecule libraries for their ability to block bind
46 mal and malignant T lymphoblasts to screen a small molecule library for activity against immature T c
47 idate the method by successfully screening a small molecule library for compounds capable of inhibiti
48 ssible therapeutic agents, we have assayed a small molecule library for in vitro inhibition of Cdc25.
49 hological settings, we previously screened a small molecule library for novel autophagy-enhancing fac
50 c domain (MUC1-CD) was established to screen small-molecule libraries for compounds that block its di
51                                    Screening small-molecule libraries for compounds that induce a phe
52 toring protease activity in the screening of small-molecule libraries for protease inhibitors.
53 an HDAC inhibitor as an enhancer to screen a small-molecule library for compounds inducing neuroblast
54 ilding on this foundation, we interrogated a small-molecule library for compounds that prevent DEPTOR
55                               In screening a small-molecule library for inhibitors of platelet activa
56 ospho-specific flow cytometry, we screened a small-molecule library for inhibitors of T cell-receptor
57 has allowed rapid screening of a 1990-member small-molecule library for inhibitors.
58 aign was conducted to interrogate a 380,000+ small-molecule library for novel D2 dopamine receptor mo
59                          A pilot screen of a small molecule library from the National Cancer Institut
60                  The increasing diversity of small molecule libraries has been an important source fo
61 ation method for construction of DNA-encoded small-molecule libraries has been developed.
62   Advances in the synthesis and screening of small-molecule libraries have accelerated the discovery
63                                A screen of a small molecule library identified two compounds that all
64                                 Screening of small-molecule libraries in this readout system revealed
65  uracil recognition mechanism to build large small-molecule libraries in which uracil is tethered via
66 f one bead-one compound (OBOC) combinatorial small molecule libraries is described here, whereby libr
67 ombine and create "de novo" kinase inhibitor small molecule libraries is described.
68                                 Screening of small-molecule libraries is an important aspect of probe
69 high-throughput screening of 39,000-compound small molecule libraries, leading to identification of f
70                             The screening of small molecule libraries led to the identification of co
71               High-throughput screening of a small molecule library led to the identification of an a
72         High-throughput screening (HTS) of a small molecule library led to the identification of aryl
73 vae to in vivo high-throughput screenings of small molecule libraries makes these models a valuable t
74 proach, we identified several molecules in a small molecule library of 10 000 compounds that could in
75 , we performed phenotypic screens on a NINDS small molecule library of 1040 drugs.
76 lecular model was used to virtually screen a small molecule library of 13 000 compounds.
77                                       Here a small molecule library of 500,000 small molecule compoun
78 luciferase complementation assay to screen a small molecule library of kinase inhibitors against the
79 ds were obtained from commercially available small-molecule libraries (Prestwick and Chembridge).
80 interest, while high-throughput screening of small molecule libraries provides potential inducers.
81 cal approach by synthesizing and screening a small molecule library, reminiscent of the polycyclic in
82 differentiation assay was screened against a small molecule library resulting in a 1,4-dihydropyridin
83  failed to reveal any druggable targets, the small-molecule library screen identified a class of alky
84 acetate HIF-1 inhibitors identified from the small-molecule library screen were also found to target
85 K-3alpha) in AML by performing 2 independent small-molecule library screens and an shRNA screen for p
86  translation of DNA sequences into synthetic small-molecule libraries suitable for in vitro selection
87  by high-throughput screening of fluorescent small-molecule libraries synthesized with a diversity-or
88                                            A small-molecule library, synthesized using this reaction,
89 imetic library as an integral component of a small-molecule library targeting protein-protein interac
90 turn mimetic library as a key component of a small-molecule library targeting the major recognition m
91 fficient construction of performance-diverse small-molecule libraries that are enriched in bioactives
92 SC668036) from the National Cancer Institute small-molecule library that can bind to the Dvl PDZ doma
93 oughput screening of synthetic combinatorial small molecule libraries to identify inhibitors of arena
94 rformed structure-based virtual screening of small-molecule libraries to seek inhibitors of the Pfn1-
95            We performed virtual docking of a small-molecule library to a site on Gbetagamma subunits
96 he virus life cycle and enables screening of small-molecule libraries under biosafety containment lev
97  identify AML1-ETO modulators, we screened a small molecule library using a chemical genomic approach
98                         We screened a 30,355 small-molecule library using a multilayered multiple mye
99                                            A small molecule library was screened for inhibition of Lc
100 MR-based screening approach on a preselected small-molecule library, we identified several compounds
101 e database and seven computationally derived small molecule libraries were used to evaluate this appr
102 een of the National Cancer Institute 140,000 small-molecule library were tested in a 96-well plate EL
103                    It has evolved to provide small molecule libraries, which, with the concomittant u
104 challenge by creating a fully functionalized small-molecule library whose membership is endowed with:
105   To validate this methodology, a model OBOC small molecule library with 12,288 members was synthesiz
106         A high-throughput screen of multiple small molecule libraries yielded several hits that marke

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