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1  which BMP4 inhibits Tolloid enzyme activity noncompetitively.
2 e receptor's regulatory site and inhibits it noncompetitively.
3 of STR, suppressed both the peak and SS IGly noncompetitively.
4 ferin, whereas myristyl alcohol inhibited it noncompetitively.
5 mma and G(t betagamma) bind to G(t alpha)GDP noncompetitively.
6 g., G protein) and inhibit agonist responses noncompetitively.
7 s reveal that the molecules inhibit Pol beta noncompetitively.
8  the apical and C-terminal regions of AgI/II noncompetitively adhere.
9 (rho-TIA) was shown previously to antagonize noncompetitively alpha(1B)-adrenergic receptors (ARs).
10                           Despite inhibiting noncompetitively, an AsnEDA inhibitor binds the active s
11 duct inhibition studies, thymidine inhibited noncompetitively and inorganic phosphate inhibited compe
12 of endocytosis, the actin cytoskeleton, acts noncompetitively as a modulator of clathrin function.
13 ribed by a model in which MMOR and MMOB bind noncompetitively at distinct interacting sites on the hy
14                                     Ibogaine noncompetitively blocked (IC50 approximately 20 nM) 22Na
15 uggest that CL-20 initiated neurotoxicity by noncompetitively blocking the ligand-gated GABA(A) recep
16 hese compounds inhibit the alpha3beta4 nAChR noncompetitively, but do not act as channel blockers, su
17 ntrations to sustain transport, is inhibited noncompetitively by 5-HT, and is more sensitive to SERT
18  complexes, regulate this enzymatic activity noncompetitively by binding at a site distinct from the
19 trans-Dimethyldiazene reduction is inhibited noncompetitively by CO and C2H2 with Ki values of ca. 0.
20 ties, inhibited serotonin transporter (SERT) noncompetitively by decreasing V(max) with little change
21 olipid hydroperoxide substrate was inhibited noncompetitively by mercaptosuccinate with K(i) 4 miroM.
22 it proteolytic activities of gamma-secretase noncompetitively by unknown mechanisms.
23 ulators (NAMs) targeting secondary sites may noncompetitively downregulate muOR activation.
24 ocking of the receptor with transferrin (Tf) noncompetitively, i.e., independently of receptor occupa
25 epopulating function either competitively or noncompetitively in irradiated hosts.
26                         PK11195 and CSA bind noncompetitively in Pgp-expressing cells, indicating tha
27                              Compound 1 acts noncompetitively in Schild analysis.
28 hown to inhibit serotonin transporter (SERT) noncompetitively, in contrast to all other known inhibit
29  one selected peptide specifically binds and noncompetitively inactivates DNA-PKcs, a protein kinase
30 ythroidine inhibits morantel-evoked currents noncompetitively, indicating that morantel does not bind
31 ntifungal drugs are the echinocandins, which noncompetitively inhibit beta-glucan synthase, a membran
32 physiological concentrations of nicotinamide noncompetitively inhibit both Sir2 and SIRT1 in vitro.
33 lpha1A- and alpha1B-adrenergic receptors and noncompetitively inhibit receptor activation by the endo
34  conditions, it can competetively inhibit or noncompetitively inhibit the enzyme.
35 asures of S1P(1) activation by CYM-5442 were noncompetitively inhibited by a specific S1P(1) antagoni
36                                     PlsY was noncompetitively inhibited by palmitoyl-CoA.
37 mology experiments verify that the enzyme is noncompetitively inhibited by resorufin.
38 [(3)H]PN200 binding to skeletal membranes is noncompetitively inhibited by TCS in the same concentrat
39 nt competitively inhibited MgATP binding and noncompetitively inhibited Fru-6-P binding.
40  peptide containing residues 311-325 (VP311) noncompetitively inhibited prothrombin activation by fac
41 ch as GTP and GDP, as well as pyrophosphate, noncompetitively inhibited sAC.
42 zolo[ 4,5-c]pyridin-4(5H)-one (MMPIP), which noncompetitively inhibited the activity of orthosteric a
43                                          K31 noncompetitively inhibited the interaction between the p
44 ced by the methylation of catecholestrogens, noncompetitively inhibited the O-methylation of 2- and 4
45 ular assays to identify small molecules that noncompetitively inhibited the receptor without reducing
46                                          GFZ noncompetitively inhibited this L. pneumophila FabI homo
47                                     Ibogaine noncompetitively inhibited transport by both SERT and th
48 ubsequent VLDL/LDL secretion by directly and noncompetitively inhibiting hepatocyte diacylglycerol ac
49 inhibition in binding to beta-tubulin, while noncompetitively inhibiting the binding of vinblastine a
50 resembles most other antimitotic peptides in noncompetitively inhibiting the binding of vinblastine t
51                                 Thus rho-TIA noncompetitively inhibits alpha(1B)-ARs but competitivel
52 l potently (IC(50) ~360 nm), reversibly, and noncompetitively inhibits ATP turnover, actin binding du
53                  Addition of 10 microM MnCl2 noncompetitively inhibits DPC photooxidation at the high
54                                         TPSF noncompetitively inhibits estrogen-dependent ERalpha-med
55                   We further show that P-CoA noncompetitively inhibits mitochondrial ADP transport an
56 and norepinephrine reuptake transporters and noncompetitively inhibits nicotinic acetylcholine and se
57  a photoactivatable analogue of octanol that noncompetitively inhibits nicotinic acetylcholine recept
58                Overall, we conclude that DPA noncompetitively inhibits NMDA-induced current by a nove
59 uring C-lignin biosynthesis, caffeyl alcohol noncompetitively inhibits oxidation of coniferyl alcohol
60                        Mechanistically, TMAO noncompetitively inhibits S-adenosylhomocysteine hydrola
61  tricyclic antidepressant (TCA) clomipramine noncompetitively inhibits substrate uptake.
62 roglitazone directly interacts with NTCP and noncompetitively interferes with NTCP-mediated bile acid
63                             Individual cells noncompetitively internalize both stimulatory and suppre
64 t studies indicated that most inhibitors act noncompetitively or uncompetitively versus substrate in
65 peripheral nicotinic acetylcholine receptors noncompetitively, primarily via an open-channel block me
66 creening hits appear non-drug-like: they act noncompetitively, show little relationship between struc
67 ies revealed that these compounds inhibit RT noncompetitively, through a new mechanism via closing of
68 A and ribosomes are bound simultaneously and noncompetitively to a common set of inactive translocons
69 14, and REGN5715 bind with high affinity and noncompetitively to Bet v 1.
70 ow density lipoprotein (LDL) receptor (LDLR) noncompetitively to cucurbit[7]uril (CB[7]) to develop a
71 structurally diverse set of drugs, which act noncompetitively to perturb normal RT function.
72 etitively when paraoxon is the substrate and noncompetitively when VX is the substrate.
73                Aptamer xPSM-A9 inhibits PSMA noncompetitively with an average K(i) of 2.1 nM, whereas
74 of Cdc25A protein phosphatase reversibly and noncompetitively with an IC(50) value of 2.2 microM.
75 nesthetics inhibited it in millimeter ranges noncompetitively with luciferin.
76 trast, AMP weakly inhibits the basic isozyme noncompetitively with respect to all substrates.
77 f phytohemagglutinin (PHA) activated T cells noncompetitively with respect to cytokine by blocking th
78  previously characterized as inhibiting 3HNR noncompetitively with respect to its naphthol substrate.
79 tively with respect to ATP concentration and noncompetitively with respect to luciferase concentratio
80 ovel NS5B inhibitor that binds to the enzyme noncompetitively with respect to nucleotide substrates.
81 hydroxysteroids, 3beta-hydroxysteroids acted noncompetitively with respect to potentiating steroids a
82 ta5 complexes and Gbetagamma dimers interact noncompetitively with the intracellular domain of GIRK c
83     Mechanistically, PA inhibited the enzyme noncompetitively with the kinetics of a tight binding in
84                Cocaine inhibits the receptor noncompetitively, with an apparent KI of 84 and 26 micro