Hydrolysis of 2-hydroxy-4-(methylthio)butanoic acid (HMB) dimer was observed in two model systems that were designed to emulate in vivo conditions. A physiologically feasible rate of hydrolysis of this methionine precursor has not previously been demonstrated in vivo. In the first model, simulated intestinal fluid (SIF) was used, and in the second model, sections of chick small intestine were incubated in vitro with the compound under study. When HMB dimer was incubated with SIF, hydrolysis was very rapid until half of the dimer was hydrolyzed. Subsequent hydrolysis was negligible in that model system. In contrast, hydrolysis neared completion when sections of small intestine were incubated with HMB dimer. These results indicate that studies of HMB dimer cleavage must include consideration of enzymatic hydrolysis factors.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.3382/ps.0651749 | DOI Listing |
Inorg Chem
February 2018
Department of Chemistry, Shahid Beheshti University, Evin, Tehran 19839-69411, Iran.
Reaction of [Pt(κ-C,N-ppy)(dmso)Cl], 1 (Hppy = 2-phenylpyridine), with Na[HB(mb)] (Hmb = 2-mercapto-benzimidazole) smoothly afforded the complex {[(κ-S,B,S-HB(mb)]Pt(κ-C,N-ppy)H}, 2, featuring a strong reverse-dative Pt → B σ interaction in the solid state. When dissolved in thf (or acetone) solution, 2 undergoes a reversible Pt-H bond activation, establishing an equilibrium between the hexacoordinated 2 and the tetracoordinate complex {[(κ-S,S-HB(mb)]Pt(κ-C,N-ppy)}, 3, as ascertained by multinuclear NMR. Hydrolysis of the B-N bond in 2/3 resulted ultimately in the formation of a dimeric half-lantern platinum(II,II) complex [{Pt(κ-C,N-ppy)(μ-κ-N,S-mb)}], 4.
View Article and Find Full Text PDFFront Chem
October 2017
The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC, Australia.
Antisense oligonucleotide (ASO)-based drug development is gaining significant momentum following the recent FDA approval of Eteplirsen (an ASO based on phosphorodiamidate morpholino) and Spinraza (2'--methoxyethyl-phosphorothioate) in late 2016. Their attractiveness is mainly due to the backbone modifications which have improved the characteristics of oligonucleotide drugs. Another class of ASO, based on peptide nucleic acid (PNA) chemistry, is also gaining popularity as a platform for development of gene-specific therapy for various disorders.
View Article and Find Full Text PDFChemistry
March 2014
School of Science and Technology, Chemistry Section, University of Camerino, S. Agostino 1, 62032 Camerino MC (Italy).
[RuCl(arene)(μ-Cl)]2 dimers were treated in a 1:2 molar ratio with sodium or thallium salts of bis- and tris(pyrazolyl)borate ligands [Na(Bp(Br3))], [Tl(Tp(Br3))], and [Tl(Tp(iPr, 4Br))]. Mononuclear neutral complexes [RuCl(arene)(κ(2)-Bp(Br3))] (1: arene=p-cymene (cym); 2: arene=hexamethylbenzene (hmb); 3: arene=benzene (bz)), [RuCl(arene)(κ(2)-Tp(Br3))] (4: arene=cym; 6: arene=bz), and [RuCl(arene)(κ(2)-Tp(iPr, 4Br))] (7: arene=cym, 8: arene=hmb, 9: arene=bz) have been always obtained with the exception of the ionic [Ru2 (hmb)2-(μ-Cl)3][Tp(Br3)] (5'), which formed independently of the ratio of reactants and reaction conditions employed. The ionic [Ru-(CH3OH)(cym)(κ(2)-Bp(Br3))][X] (10: X=PF6, 12: X=O3SCF3) and the neutral [Ru(O2CCF3)(cym)(κ(2)-Bp(Br3))] (11) have been obtained by a metathesis reaction with corresponding silver salts.
View Article and Find Full Text PDFDalton Trans
November 2012
Department of Chemistry, University of Ottawa, 10 Marie-Curie, Ottawa, ON K1N 6N5, Canada.
A mononuclear as well as dinuclear Dy(III) complexes of general formula [Dy(hmb)(NO(3))(2)(DMF)(2)] (1) and [Dy(2)(hmt)(NO(3))(4)(DMF)(4)]·DMF (2), where Hhmb: (N'-(2-hydroxy-3-methoxybenzylidene)benzohydrazide and H(2)hmt: (N(1),N(4))-N'(1),N'(4)-bis(2-hydroxy-3-methoxybenzylidene)terephthalohydrazide were obtained using a synthetic strategy involving a polytopic Schiff base ligand. Single-crystal X-ray analysis reveals the Dy(III) ion is in a distorted pentagonal interpenetrating tetrahedral arrangement. The two symmetrical Dy(III) ions in complex 2 exhibit the same geometry and are well-isolated in the molecule by an hmt(2-) ligand.
View Article and Find Full Text PDFInorg Chem
June 2010
School of Chemistry, Monash University, Victoria, Clayton 3800, Australia.
5-Hydroxy-1,3-diketonate ligands have been found to stabilize dimeric complexes and tetrameric lanthanoid clusters dependent on the degree of steric bulk provided by the presence or absence of a methoxy group. Treatment of (R/S,Z)-1'-hydroxy-3-(hydroxy(phenyl)methylene)bi(cyclopentan)-2-one (Hhpb) and the p-methoxyphenyl derivative (Hhmb) with [LnCl(2)(H(2)O)(6)]Cl yields clusters of composition [Ln(4)(Cl)(2)(O)(hpb)(6)]Cl(2) (Ln = Nd (1), Ho (2), Tb (3), and Er (4)) and [Ln(2)(hmb)(5)]Cl (Ln = La (5), Nd (6), Tb (7), Dy (8), and Er (9)). Single crystal X-ray analysis of the tetranuclear cluster has revealed the lanthanoid core to be in a tetrahedral arrangement around a central mu(4)-oxygen, bridged by symmetrical chlorides and shrouded in six bridging hpb ligands.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!