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1 d with the specific protease inhibitor bis(5-amidino-2-benzimidazo-lyl)methane (BABIM) markedly atten
2  protease (dMCP)-3, i.e., aprotinin or bis(5-amidino-2-benzimidazolyl) methane (BABIM), did not.
3 dazolyl)methane ketone, and hemi-BABIM is (5-amidino-2-benzimidazolyl)(2-benzimidazolyl)methane), and
4                  One such inhibitor is bis(5-amidino-2-benzimidazolyl)methane (BABIM), standing out a
5 n a manner similar to that reported by bis(5-amidino-2-benzimidazolyl)methane (BABIM).(1) Alternative
6 -benzimidazolyl)methane, keto-BABIM is bis(5-amidino-2-benzimidazolyl)methane ketone, and hemi-BABIM
7 a potential metalloprotease inhibitor, bis(5-amidino-2-benzimidazolyl)methane, and provide snapshots
8 , and -hemi-BABIM-Zn2+ (where BABIM is bis(5-amidino-2-benzimidazolyl)methane, keto-BABIM is bis(5-am
9 stal structures with nafamostat, '157, and 6-amidino-2-naphthol.
10 roadly acting pancreatic enzyme inhibitor (6-amidino-2-naphthyl p-guanidinobenzoate dimethanesulfate,
11 emic mixture of inhibitor FX-2212, (2RS)-(3'-amidino-3-biphenylyl)-5-(4-pyridylamino)pentanoic acid,
12 el series of fXa inhibitors incorporating an amidino 6,5-fused bicyclic moiety at the P1 position has
13 rence for linear aliphatic polyamines as the amidino acceptor substrate, especially for spermidine an
14 ng HAuCl4 with a CO2-responsive monomer N-(3-amidino)-aniline (NAAN).
15 sent a new CO2-responsive polymer, poly(N-(3-amidino)-aniline) (PNAAN), coated gold NPs (AuNPs) synth
16 r, unlike previously described guanidino- or amidino-based inhibitors which have pK(a) values greater
17                   Several 5-guanidino- and 5-amidino-based oseltamivir derivatives were synthesized a
18  and synthesized a series of symmetric bis-6-amidino-benzothiazole derivatives with aliphatic central
19 inobenzylidene)cycloheptanone, and 2,8-bis(4-amidino- benzylidene)cyclooctanone.
20 alent bond formation between the inhibitor's amidino carbon and the active-site Cys274, and solution
21                                          The amidino compounds L-N6-(1-iminoethyl)lysine, L-N5-(1-imi
22                                Additionally, amidino derivative 3a (Cbz-l-Leu-l-Phe-CONH-d-CH[C(NH)NH
23 dom copolymer poly(dimethyl acrylamide-co-(N-amidino)ethyl acrylamide), or P(DMA-co-NAEAA), containin
24 inked to the positively charged guanidino or amidino functionalities.
25 s enhanced van der Waals interactions in the amidino furan-DNA complex.
26 creening dose of 10 micromol/kg, 4 of the 12 amidino furans described here are more active than the p
27 of creatine biosynthesis: the transfer of an amidino group from arginine to glycine to form ornithine
28 chemical moiety other than a guanidino or an amidino group.
29  lifetime is attributed to distortion of the amidino groups in this complex, resulting in less effici
30 rays contain 6-12 carboxylic acid groups, 12 amidino groups, 6 thiol groups, or 6 thiol groups and 6
31         The most promising compounds were (4-amidino)-L-phenylalanine-containing inhibitors, which re
32        Substitution of an alkyl group of the amidino nitrogen, except for in 9, 13, and 15, resulted
33 stem in the absence of a substitution of the amidino nitrogens resulted in higher affinity for DNA th
34                                          The amidino P1 residue D,L-(4-AmPhGly)P(OPh)2 was utilized i
35  to gp120 residues 421-431 with a C-terminal amidino phosphonate diester mimetic of the Lys(432)-Ala(
36 by formation of covalent adducts of a hapten amidino phosphonate diester was attributed to micro and
37 iles has been used to generate over 50 novel amidino-rocaglate (ADR) and amino-rocaglate derivatives.