Synthesis of 5′-benzoyl-2′-hydroxychalcones and related flavonoid compounds

Summary 5 -Benzoyl-2 -hydroxychalcones were synthesized by the condensation of 5 -benzoyl-2 -hydroxyacetophenone with aromatic aldehydes in presence of an ethanolic solution of potassium hydroxide. Derivatives of 6-benzoylflavonoids were prepared from chalcones.     

Semicarbazone and thiosemicarbazone chromium(III) complexes

Summary Chromium(III) complexes, [Cr(ligand)₂]Cl, containing the semicarbazones and thiosemicarbazones of 2-hydroxyacetophenone and 2-hydroxynaphthaldehyde, and [Cr(ligand)₂Cl₂]Cl, formed from 4-hydroxyacetophenone semicarbazone and thiosemicarbazone, have been synthesized. The complexes were characterized by elemental analysis, conductance, magnetic moment, i.r., electronic and e.s.r. spectral studies. On the basis of physicochemical investigations tetragonal geometries are assigned to the complexes.     

Thermal Investigations of nBABAs

The phase transitions occurring in nBABAs (n = 1 to 5), especially those involving the nematic phase, have been studied by DSC. Schemes of transition are presented and the chain length (n) dependences of the the transition temperatures and entropies are discussed.     

Stereospecific Synthesis of Endo-6-Aryl-2-Oxobicyclo [3.3.1]Nonanes

Two alternate synthetic routes to endo-6-aryl-2-oxobicyclo 3.3.1 nonan [3a-d] by sterespecific catalytic hydrogenetion of the easily accessible 6-arylbicyclo 3.3.1 nona-3,6-dien-2-ones [2a-d], and regioselective oomologation of endo-2-aryl-6-oxobicycle 3.2.1 octanes [4a-d] are described.     

N,N,N′-Tri­methyl­ethyl­enediammonium dichloride

The title compound, C₅H₁₆N₂²⁺·2Cl⁻, was isolated as a by-product from the reaction between trimethylethyl­enedi­amine and germanium tetrachloride in the presence of triethyl­amine. The asymmetric unit contains two cations, one in the gauche and the other in the trans conformation; these conformations are stabilized by hydrogen-bonding interactions between the N—H moieties and the chloride anions.     

Effect of peptide-based captopril analogues on angiotensin converting enzyme activity and peroxynitrite-mediated tyrosine nitration

Angiotensin converting enzyme (ACE) regulates the blood pressure by converting angiotensin I to angiotensin II and bradykinin to bradykinin 1-7. These two reactions elevate the blood pressure as angiotensin II and bradykinin are vasoconstrictory and vasodilatory hormones, respectively. Therefore, inhibition of ACE is an important strategy for the treatment of hypertension. The natural substrates of ACE, i.e., angiotensin II and bradykinin, contain a Pro-Phe motif near the site of hydrolysis. Therefore, there may be a Pro-Phe binding pocket at the active site of ACE, which may facilitate the substrate binding. In view of this, we have synthesized a series of thiol- and selenol-containing dipeptides and captopril analogues and studied their ACE inhibition activities. This study reveals that both the selenol or thiol moiety and proline residues are essential for ACE inhibition. Although the introduction of a Phe residue to captopril and its selenium analogue considerably reduces the inhibitory effect, there appears to be a Phe binding pocket at the active site of ACE.     

Pd(II)-mediated assembly of porphyrin channels in bilayer membranes

A membrane-spanning bis(meso-3-pyridyl) porphyrin 1 has been synthesized, embedded in EYPC vesicles, and upon Pd(II) addition has been shown to form ionophores that allow the passage of anionic 5/6-carboxyfluorescein through membranes. The geometric matching of bis(meso-3-pyridyl) porphyrin 1 and trans-Pd(II) was designed to give a cyclic porphyrin trimer [PdCl(2)(1)](3). However, solution-phase studies showed that PdCl(2)(PhCN)(2) cross linked 1 into linear oligomers at porphyrin concentrations above 10 mM, although the formation of cyclic species was inferred from studies at concentrations below 2 μM. Fluorescence titrations showed that embedding porphyrin 1 in bilayers greatly reduced its affinity for Pd(II), but the combination of porphyrin 1 and Pd(II) gave an ionophoric species that increased the rate of 5/6-carboxyfluorescein (5/6-CF) transit through the phospholipid bilayer 12-fold. A maximum in the 5/6-CF release rate was observed at a Pd(II) concentration of 4 μM, and the application of a solution-phase binding model to the membrane phase showed that this peak in ionophoric activity corresponded to the greatest extent of porphyrin oligomerization. Further studies suggested these Pd(II)/porphyrin oligomers transported 5/6-CF via a channel mechanism.     

Study of the effect of SHI irradiation on nanocrystalline vacancy doped (La,Sr)(Mn,Fe)O system and its comparison with hydrostatic pressure using Mössbauer spectroscopy

The swift heavy ion irradiated La_0.9Mn_0.8Fe_0.2O₃ (La-deficient) system with 200 Mev Ag^16?+? ion beam at fluence 5 × 10¹² ions/cm² was studied with X-ray diffraction (XRD) and Mössbauer spectroscopic measurements. Comparison of Mössbauer parameters with those of unirradiated sample showed an increase in line width on irradiation which may be due to reduction in particle size as well as due to creation of defects. An increase in quadrupole splitting with no appreciable change in isomer shift showed ion-induced structural disorder in the material after irradiation. An attempt is made to compare the effect of fluence with the hydrostatic pressure on the sample.