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

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