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1 enerator, AAPH (2,2'-azobis(2-amidinopropane)dihydrochloride).
2 he mitochondria-targeting compound alexidine dihydrochloride.
3 rosslinking and functionalized by cysteamine dihydrochloride.
4 ro-5-(4-puridinyl)imidazo(2, 1-beta)thiazole dihydrochloride.
5 de, in comparison with original mitoxantrone dihydrochloride.
6 g imatinib, mycophenolic acid and quinacrine dihydrochloride.
7 etection of 2.9 x 10(-12) M for mitoxantrone dihydrochloride.
8 er-the-counter antihistamine drug cetirizine dihydrochloride.
9 -[4-(2-piperidinylethoxy)phenol]-1H-pyrazole dihydrochloride.
10  were blocked by N-(1-naphtyl)ethylendiamine dihydrochloride.
11  available (2S)-piperazine-2-carboxylic acid dihydrochloride.
12 ed to beta,beta-difluorohistamine (2) as the dihydrochloride.
13 roup provide beta-fluorohistamine (1) as the dihydrochloride.
14 yl arginine and L-N(6)-(1-iminoethyl) lysine dihydrochloride.
15            Amisulpride (400 mg), pramipexole dihydrochloride (0.5 mg), or placebo were administered i
16 nel blockers NiCl2 (50 microM) or mibefradil dihydrochloride (10 microM) affected the amplitude of ex
17 1 receptor agonist 2-(2-aminoethyl) thiazole dihydrochloride (10 microM) and blocked by the H1 antago
18 agonists N-(3-aminomethyl) benzylacetamidine dihydrochloride (1400W) and aminoguanidine (AG) and a no
19 hibitor N-(3-(aminomethyl)benzyl)acetamidine dihydrochloride (1400W) and the specific guanylyl cyclas
20 -4-yloxy)phenyl]-2-(morpholin-4-yl)acetamide dihydrochloride (17v, SUVN-G3031) as a clinical candidat
21                  N-(1-naphtyl)ethylendiamine dihydrochloride (5 microM), a specific iNOS inhibitor, l
22 ly with a BN or PL with 10mg/ml of histamine dihydrochloride, 50% glycerosaline control, and JCP extr
23 nding and 3-(2(S)-azetidinylmethoxy)pyridine dihydrochloride (A85380)-resistant [125I]epibatidine-bin
24 ted with 2,2'-azobis(2-methylpropionamidine) dihydrochloride (AAPH) and thermal pasteurization was ca
25  the mAbs with 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) in formulations containing l-meth
26 rating system, 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) led to increases of 2% or 30% in
27 ogical model as 2,2'-azobis (2-aminopropane) dihydrochloride (AAPH) or Fe(+3)/Ascorbic acid (Fe(+3)/A
28 ), and 2,2'-azobis-2-methyl-propanimidamide, dihydrochloride (AAPH) radicals and nitric oxide (NO).
29 ) oxidation by 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) resulted in a loss of high-affini
30 cal initiator, 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH).
31 treatment with 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH).
32 nerator 2,2'-azobis(2-methyl propionamidine) dihydrochloride (AAPH).
33 ical initiator (2,2'-azobis(2-amidinopropane)dihydrochloride; AAPH), pointing toward a mechanism, whe
34 dation catalyzed by azobis(2-amidinopropane).dihydrochloride (ABAP) or by copper.
35 olidin-2-yl]-1H-benzimidazole-4-carboxamide, dihydrochloride; Abbott Laboratories, Abbott Park, IL),
36 ethyl-3-(2-(S)-pyrrolindinylmethoxy)pyridine dihydrochloride (ABT-089), a clinically effective cognit
37 ,2,4]triazolo[3,4-f][1,6]naphthyri din-3-one;dihydrochloride; allosteric inhibitor) or with small int
38 (4)-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride), an inhibitor of SMOX, reduced gastric
39  Here, we show that treatment with alexidine dihydrochloride, an antibiotic and a selective inhibitor
40       Addition of N6-(1-iminoethyl)-L-lysine dihydrochloride, an iNOS inhibitor, significantly enhanc
41 n the presence of Phe-Arg-beta-naphthylamide dihydrochloride and 1-(1-naphthylmethyl)-piperazine indi
42 Azetidinylmethoxy]-3-pyridinyl]-5-hexyn-1-ol dihydrochloride and 4-(5-ethoxy-3-pyridinyl)-N-methyl-(3
43 en 2,5,6-triamino-3,4-dihydropyrimidin-4-one dihydrochloride and D-galactose phenylhydrazone to give
44 vity by spectrophotometry with o-dianisidine dihydrochloride and hydrogen peroxide at 460 nm.
45  agents (2,2'-azobis, 2-methylpropionamidine dihydrochloride and hydrogen peroxide).
46 otection, from 2,2'-azobis(2-amidinopropane) dihydrochloride and inhibited acetylcholinesterase activ
47 s evaluated by 4',6-diamidino-2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferas
48    Membrane fractions treated with alexidine dihydrochloride and thonzonium bromide fully retained co
49 a g)) with the Pyd substitutes, pyridoxamine dihydrochloride and vitamin B(6), which share the same c
50 noethyl) indolin-4-yl ethyl(methyl)carbamate dihydrochloride) and 94 (3-(3-methoxy-3-oxopropyl)-4-(((
51 y using DAPI (4',6-diamindino-2-phenylindole dihydrochloride) and Annexin V staining, along with acti
52 rophenyl)-1H-imidazol-5-yl]-2-pyrimidinamine dihydrochloride), and KNK437 (N-Formyl-3,4-methylenediox
53 dro-1H-imidazol-2-yl)amin o)phenyl)benzamide dihydrochloride] and 2 [N-(3-chloro-4-((4,5-dihydro-1H-i
54 arkethyl)phenyl]-2-thiophenecarbo ximidamide dihydrochloride (ARL 17477) on recombinant human neurona
55 fanilamide and N-(1-naphthyl)ethylenediamine dihydrochloride as color reagents where the samples thro
56 y was to assess the effect of oral azimilide dihydrochloride (AZ) 100 mg versus placebo on the onset,
57 his study evaluated the effects of azimilide dihydrochloride (AZ) on anti-tachycardia pacing (ATP) an
58 dentify an anti-cancer drug of bis-biguanide dihydrochloride (BBD) as potent anti-mycobacteria agent.
59 3,4-dichlorophenyl)ethyl]-4-methylpiperazine dihydrochloride (BD-1063) and haloperidol and by pertuss
60 nnamylamino)ethyl]-5-isoquinolinesulfonamide dihydrochloride but not by the cAMP exchange protein inh
61 idyl)-4-(1-aminoethyl)cyclohexanecarboxamide dihydrochloride)]} but not by an inhibitor of farnesyl-t
62 -(5-isoquinolinesulfonyl)-2-methylpiperazine dihydrochloride] but not by H8 [N- inverted question mar
63 -(CBZ-L-isoleucyl-L-prolyl-L-arginine amide) dihydrochloride (BZiPAR) was used to detect trypsinogen
64 uoromethyl -2-imidazolyl)phenoxy]-2-propanol dihydrochloride (CGP-20712A) prevented isoproterenol-ind
65  nuclear stain 4',6-diamidine-2-phenylindole dihydrochloride (DAPI) and imaged with a fluorescence mi
66 enumerated by 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI) staining, and phagosome-lysosome
67 SYPRO Ruby and 4',6-diamidino-2-phenylindole dihydrochloride (DAPI), to detect proteinaceous and micr
68 odide (PI) or 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI).
69                        The PKA inhibitor H89 dihydrochloride did not affect the average mIPSC amplitu
70 ppeastrine hydrobromide (HH) and amodiaquine dihydrochloride dihydrate (AQ) can inhibit ZIKV infectio
71 buryport, MA) that was labeled and sold as a dihydrochloride dihydrate was in fact the monohydrochlor
72 mine the crystal structure of Levocetirizine dihydrochloride directly from crystalline powders that w
73    3-[(2,4-dimethoxy)benzylidene]-anabaseine dihydrochloride (DMXBA; GTS-21), an Alzheimer's drug can
74                    Two inhibitors, alexidine dihydrochloride (EC(50) = 39 muM) and thonzonium bromide
75 logical restoration of Eepd1 with Retigabine dihydrochloride effectively mitigates obesity.
76 nd (4) 10 mm N(5)-(1-iminoethyl)-l-ornithine dihydrochloride [endothelial NOS (eNOS) inhibitor].
77 namyl-amino)ethyl]-5-isoquinolinesulfonamide dihydrochloride) enhanced the basal strength of coupling
78 at reacts with N-(1-naphthyl)ethylenediamine dihydrochloride forming an orange-colored product absorb
79 tyl-7-(O-[N-methylpiperazino]-gamma-butyryl)-dihydrochloride-forskolin (MPB-forskolin), we found that
80 lo[4,5-h][2,3]benzodazepin-5-yl)-benzenamine dihydrochloride (GYKI52466)] antagonists into the DMH.
81 5-isoquinolinylsulphonyl)-2-methylpiperazine dihydrochloride (H-7; 10 microM).
82 )amino)ethyl]-5-isoquinolinesulphonamide+ ++ dihydrochloride (H-89; 1 microM), and abolished by inclu
83 namyl-amino)ethyl]-5-isoquinolinesulfonamide dihydrochloride (H89), or with the Golgi-disturbing agen
84 yl-7-azabicyclo[2.2.1]heptano[2,3-c]pyridine dihydrochloride has been prepared enantiospecifically fr
85 hoxyphenthyl)]-4-(3-phenylpropyl)-piperazine dihydrochloride) in tumor and brain and to evaluate the
86 rted question mark-5-isoquinolinesulfonamide dihydrochloride], indomethacin, or nordihydroguaiaretic
87                                    Azimilide dihydrochloride is a class III antiarrhythmic drug posse
88 ynthase inhibitors S-methyl-L-thiocitrulline dihydrochloride (L-MIN) or 7-nitroindazole monosodium sa
89 cific inhibitor, N6-(1-iminoethyl)-L-lysine, dihydrochloride (L-NIL) solely restricts lung protein ni
90   The addition of N6-(1-iminoethyl)-l-lysine dihydrochloride (L-NIL), the iNOS inhibitor, significant
91 (4-fluorophenyl)methyl]-4-cinnamylpiperazine dihydrochloride (LDK1203) and 1-[bis(4-fluorophenyl)meth
92 eptor agonist, 1-(3-Chlorophenyl) piperazine dihydrochloride (m-CPP), for 1 week resulted in a decrea
93                                    Azimilide dihydrochloride may be a safe and effective drug for red
94 te nuclei with 4',6-diaminido-2-phenylindole dihydrochloride (Molecular Probes, Carlsband, CA) reveal
95  MS using the N-(1-naphthyl) ethylenediamine dihydrochloride (NEDC) matrix.
96    The screen identified nor-binaltorphimine dihydrochloride (nor-BNI) and dibutyryl-cAMP, sodium sal
97  selective KOR antagonist norbinaltorphimine dihydrochloride (nor-BNI) would attenuate the escalation
98  kappa-opioid antagonist nor-Binaltorphimine dihydrochloride (nor-BNI; 100 nM), and by high concentra
99 c) cells using 4',6-diamidino-2-phenylindole dihydrochloride nuclear staining.
100 ino]methyl}-4 -biphenylyl)methyl]propanamide dihydrochloride), on prepulse inhibition of the acoustic
101 ulfanilamide/N-(1-naphthyl)- ethylenediamine dihydrochloride or 2,2'-azinobis (3-ethylbenzthiazoline-
102 thyl-3-(2-(S)-pyrrolindinylmethoxy) pyridine dihydrochloride], or the alpha7 nAChR agonist A-582941 [
103 0-bis(4-pyridinylmethyl)-9(10H)-anthracenone dihydrochloride] produced 73% inhibition at 3 microM; ne
104 MV using DAPI (4',6-diamidino-2-phenylindole dihydrochloride), propidium iodide (3,8-diamino-5-[3-(di
105                                 Pyridoxamine dihydrochloride (Pyridorin, NephroGenex) inhibits format
106 carbaldehyde with 11b gave an azulisapphyrin dihydrochloride salt in 35% yield, and this also showed
107 ght-Giemsa and 4',6-diamidine-2-phenylindole-dihydrochloride staining, that As(2)O(3) blocked the cel
108 t to thonzonium bromide but not to alexidine dihydrochloride, suggesting that this conserved sequence
109  paraquat, or 2,2'-azobis-(2-amidinopropane) dihydrochloride treatment, the MsrA overexpressed strain
110 r, and meso-tetra(4-sulfonatophenyl)porphine dihydrochloride (TSPP) as receptor, for Zn(2+) detection
111 ial to V(1)V(0) complexes and that alexidine dihydrochloride uncouples the enzyme by a different mech
112 f the precursor, bis(3-aminopropyl)disulfide dihydrochloride, used to introduce this substituent into
113                                    Azimilide dihydrochloride was generally well tolerated and did not
114                                    Azimilide dihydrochloride was investigated as adjunctive treatment
115 bolite 5-ARU (5-amino-4-d-ribitylaminouracil dihydrochloride), which is a conserved compound that act
116 (7-chloroquinolin-4-yl)benzene-1,3-diamine) (dihydrochloride), which is active against Plasmodium ber
117 mycin; and the synthetic compound, alexidine dihydrochloride, which is known to act on a mitochondria
118 -(5-isoquinolinesulfonyl)-2-methylpiperazine dihydrochloride with DAMGO did not alter the tolerance t
119 0-bis(4-pyridinylmethyl)-9(10H)-anthracenone dihydrochloride (XE-991) and linopirdine.
120 0-bis(4-pyridinylmethyl)-9(10H)-anthracenone dihydrochloride (XE991) (40 mum), in both intact males a
121 idyl)-4-(1-aminoethyl)cyclohexanecarboxamide dihydrochloride (Y27632) also attenuated SDF-1-induced E

 
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