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1 d with the specific protease inhibitor bis(5-amidino-2-benzimidazo-lyl)methane (BABIM) markedly atten
3 dazolyl)methane ketone, and hemi-BABIM is (5-amidino-2-benzimidazolyl)(2-benzimidazolyl)methane), and
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
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
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
18 and synthesized a series of symmetric bis-6-amidino-benzothiazole derivatives with aliphatic central
20 alent bond formation between the inhibitor's amidino carbon and the active-site Cys274, and solution
23 dom copolymer poly(dimethyl acrylamide-co-(N-amidino)ethyl acrylamide), or P(DMA-co-NAEAA), containin
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
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
33 stem in the absence of a substitution of the amidino nitrogens resulted in higher affinity for DNA th
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.