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Query: UMLS:C0027960 (mole)
 21,279 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Quinolinium compounds have been used as Cl-sensitive fluorescent indicators in cells and cell-free membrane fractions. To improve Cl sensitivity and for conjugation via nucleophilic reaction, the compounds 6-methoxy-N-(n-aminoalkyl)quinolinium bromide hydrochloride (AAQ) with alkyl chain lengths (n) of 2 (AEQ), 3 (APQ), and 4 (ABQ) were synthesized. AAQ was water soluble, fluorescent, and quenched by Cl. The Stern-Volmer constants (KCl) for quenching of protonated AEQ, APQ and ABQ by Cl were 354, 322, and 272 M-1, respectively, higher than KCl for 6-methoxy-N-(3-sulfopropyl)quinolinium (SPQ; 118 M-1). To eliminate pH-dependent fluorescence, 6-methoxy-N-(3-trimethylammoniumpropyl)quinolinium dibromide (TMAPQ) was synthesized (KCl, 310 M-1). To red shift fluorescence excitation and emission spectra, 6-phenyl-N-(3-trimethylammoniumpropyl)quinolinium dibromide (phenyl-TMAPQ) (emission 475 nm) and N-(3-trimethylammoniumpropyl)phenanthridinium dibromide (TMAPP) (excitation 380 nm) were synthesized. AEQ and ABQ were conjugated with neutral dextran activated by cyanogen bromide to give indicator-to-dextran mole ratios of 5 to 20. KCl values at pH 7.4 were 132 (AEQ-dextran) and 237 M-1 (ABQ-dextran). To construct a single molecule with Cl-sensitive and insensitive moieties, the bichromophores 6-methoxy-N-(n- dansylsulfonamidoalkyl)quinolinium with alkyl chains of two and four were synthesized. The new Cl-sensitive indicators were used for measurement of intracellular Cl activity and for the labeling of endocytic vesicles in 3T3 fibroblasts and T84 cells. Our results indicate that N-substitution of quinoline with positively charged moieties gives increased Cl sensitivity, and extension of ring conjugation gives indicators with red-shifted fluorescence spectra.
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PMID:Synthesis of cell-impermeable Cl-sensitive fluorescent indicators with improved sensitivity and optical properties. 137 Jul 43

Chlorophyllin (CHL), a copper/sodium salt of chlorophyll used in the treatment of geriatric patients, is an anti-mutagen that has been demonstrated to inhibit carcinogen--DNA binding in vivo. To study the mechanism of inhibition, the microsomal metabolism of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) and the kinetics of IQ--DNA binding were investigated in the presence and absence of CHL. In time-course studies, CHL produced greater than 80% inhibition of IQ--DNA binding and blocked the metabolism of IQ, such that 80% of the initial dose of carcinogen was recovered unmetabolized from the incubations after 1 h. Kinetic constants were determined for the in vitro DNA binding reaction, with the reaction rate measured as 'pmol IQ bound/mg DNA/min/mg microsomal protein'. Without altering V(max), the Km of the IQ--DNA binding reaction was increased by CHL, and the replot of Km/V(max) versus CHL concentration yielded a straight line with an inhibitor constant of 58.3 microM CHL. Spectrophotometric studies provided evidence in vitro for the formation of a non-covalent complex between CHL and IQ. The CHL--IQ complex had a stoichiometric ratio of 2:1 (mole ratio method) and an apparent dissociation constant from the Benesi-Hilderbrand plot of 1.41 x 10(-4)M at pH 7.4. These results are discussed in the context of a CHL inhibitory mechanism involving enzyme inhibition and molecular complex formation.
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PMID:Inhibition of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ)-DNA binding by chlorophyllin: studies of enzyme inhibition and molecular complex formation. 163 77

The steady-state flux of 33 substituted quinoline derivatives was determined in polydimethylsiloxane membranes using isopropyl alcohol as the receiver solvent. These diffusants constituted a diverse group of compounds possessing a wide range of hydrophobic, steric, and electronic characteristics. Various parameters representing these physicochemical properties such as cyclohexane-water fragmental constants, molar refractivity, Hammett's sigma constants, intramolecular hydrogen bonding ability, melting point, and mole fraction solubility were employed to develop empirical models capable of relating the rate of diffusion to these characteristics of either the substituent on the quinoline ring or the compound itself.
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PMID:The development of a predictive method for the estimation of flux through polydimethylsiloxane membranes. IV. Application to a series of substituted quinolines. 832 51

Chlorophyllin (CHL) is a water-soluble salt of chlorophyll that exhibits antimutagenic activity in short-term genotoxicity assays and inhibits carcinogen-DNA binding in vivo. The antimutagenic potency of CHL was studied against several structurally related heterocyclic amines using the Salmonella assay. The mutagens included 2-amino-3-methylimidazo[4,5,-f]-quinoline (IQ) and seven related IQ-type compounds, and 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2) and three additional non-IQ-type compounds. No relationship was observed between mutagenic potency (revertants/ng mutagen) and antimutagenic potency when expressed in terms of the CHL dose/plate-inhibiting mutagenicity by 50 percent (I50). However, a correlation was observed between mutagenic potency and the mole ratio of CHL to mutagen giving 50% inhibition (MR50), with most mutagens requiring several hundredfold to several thousandfold molar excess of CHL for inhibition. In spectrophotometric studies, CHL formed noncovalent molecular complexes with the heterocyclic amines, with binding constants in the range 3-13 x 10(3) M-1. Binding constants were inversely correlated with I50 and MR50 values, i.e., with increasing strength of complex formation less CHL/plate and a lower mole ratio of CHL to mutagen was required to inhibit mutagenicity. The results support an inhibitory mechanism in which chlorophylls operate as "interceptor molecules," interacting with carcinogens and mutagens directly and limiting their bioavailability.
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PMID:Antimutagenic potency of chlorophyllin in the Salmonella assay and its correlation with binding constants of mutagen-inhibitor complexes. 840 76

The interaction between DNA and a benzothiazole-quinoline cyanine dye with a trimethine bridge (TO-PRO-3) results in the formation of three noncovalent complexes. Unbound TO-PRO-3 has an absorption maximum (lambda(max)) of 632 nm, while the bound dyes (with calf thymus DNA) have electronic transitions with lambda(max) = 514 nm (complex I), 584 nm (complex II) and 642 nm (complex III). The blue shifts in the electronic transitions and the bisignate shape of the circular dichroism bands indicate that TO-PRO-3 aggregates with DNA. Complex I has a high dye:base pair stoichiometry, which does not depend on base sequence or base modifications. The bound dyes exhibit strong interdye coupling, based on studies with a short oligonucleotide and on enhanced resonance scattering. From thermal dissociation studies, the complex is weakly associated with DNA. Studies with poly(dGdC)2 and poly(dIdC)2 and competitive binding with distamycin demonstrate that complex II is bound in the minor groove. This complex stabilizes the helix against dissociation. For complex III, the slightly red-shifted electronic transition and the stoichiometry are most consistent with intercalation. Using poly(dAdT)2, the complexes have the following dye mole fractions (X(dye)): X(dye) = 0.65 (complex I), 0.425 (complex II) and 0.34 (complex III).
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PMID:Spectroscopic studies of the multiple binding modes of a trimethine-bridged cyanine dye with DNA. 1273 5

The cucurbit[7,8]urils (Q[7] and Q[8])-induced room temperature phosphorescence (RTP) of quinoline and its derivatives were firstly found in the cucurbit[n]urils chemistry. The luminophores (quinolines) and their RTP are affected by the concentration of different Q[n]s, heavy metal ions and amounts, and pH. The RTP lifetime of the luminophore has been investigated. In presence of Na2SO3, the cation Tl+ led to stronger Q[n]-induced RTP, while the RTP lifetimes of luminophore/Q[7 or 8]/KI were generally longer than that of luminophore/Q[7 or 8]/TlNO3, the RTP lifetimes of these systems were between 0.18 and 47.4 ms. Contrary to the stable 1:2 Q[8]:guest ternary inclusion complexes at lower pHs, as suggested by 1H NMR, electronic absorption and fluorescence spectroscopy, low Q[8]-induced room temperature phosphorescence was observed. However, at higher pHs, high intensity of cucurbit[n]urils-induced room temperature phosphorescence of these quinoline derivatives were observed, and a 1:1 Q[8]:guest inclusion complex was formed. Investigations of dependence of RTP intensity on concentration of Q[n] revealed that the highest intensity of the Q[n]-induced RTP was observed at a low mole ratio of host:guest, which is closed to 1:1. It was presumably resulted from the strong interaction of Q[n] and these guests due to the combined hydrophobic cavity interaction and the hydrophilic portal interaction of the cucurbit[n]urils with the nitrogen heterocycles guest.
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PMID:Cucurbit[n]urils-induced room temperature phosphorescence of quinoline derivatives. 1765 17

A procedure is described for the extractive spectrophotometric determination of nickel and palladium with quinoline-2-aldehyde thiosemicarbazone. At pH 7.5 nickel forms a 1:2 complex which is soluble in chloroform and has an absorption maximum at 460 nm. Palladium forms a 1:2 complex with maximum absorbance at 510 nm which can be extracted into MIBK from 1M HCl. Both complexes are stable and conform to Beer's law. The molar absorptivities for nickel and palladium are 1.58 x 10(4) and 2.6 x 10(3) 1.mole(-1). cm(-1) respectively. The proposed method is suitable for detection and determination of nickel and palladium in the presence of associated metal ions. The results of the analysis of synthetic mixtures and standard samples are reported.
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PMID:Quinoline-2-aldehyde thiosemicarbazone (QAT) as spectrophotometric reagent for palladium and nickel. 1896 96

A simple, rapid and selective procedure for spectrophotometric determination of cobalt has been developed. Cobalt(II) forms two water-soluble complexes with 2-[di-(2-pyridyl)methylidenehydrazino]quinoline, an orange-yellow complex (lambda(max) 510 nm) in the pH range 2-12 and a pink complex (lambda(max) 530 nm) in 0.1-6M perchloric acid medium. The molar absorptivities for the orange-yellow and pink complexes are 3.65 x 10(4) and 4.1 x 10(4) 1.mole(-1).cm(-1) and Beer's law is obeyed up to 1.84 and 2.0 ppm of cobalt(II) respectively. Cobalt(II) has also been determined in alloys.
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PMID:Spectrophotometric determination of cobalt(II) with 2-[di-(2-pyridyl)-methylidenehydrazino]quinoline. 1896 36

A simple, rapid and sensitive spectrophotometric method has been developed for the determination of platinum. 5-(4-Nitrophenylazo)-8-(p-toluenesulphonamido)quinoline (NPTSQ) reacts with platinum(II) almost instantaneously in alkaline solution to form a violet-red 1:2 complex with an absorption maximum at 640 nm. Beer's law is obeyed over the concentration range 0-1 mug/ml platinum. The molar absorptivity is 1.37 x 10(5) 1.mole(-1).cm(-1). The method has been used for the determination of microamounts of platinum in catalysts and anode slime.
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PMID:Colour reaction of platinum(II) with 5-(4-nitrophenylazo)-8-(p-toluenesulphonamido)-quinoline and its analytical applications. 1896 36

Carbonyl-modified proteins are considered markers of oxidative damage caused by oxidative stress, aging, and disease. Here we use a previously developed capillary electrophoretic method for detecting femtomole (10(-15) mole) carbonyl levels in mitochondrial proteins that are size separated and profiled. For protein labeling, carbonyls were tagged with Alexa 488 hydrazine and amine groups in proteins with 3-(2-furoyl)quinoline-2-carboxaldehyde. Total mitochondrial protein carbonyl levels were statistically higher in fast- than in slow-twitch muscle of young Fischer 344 rats, and statistically higher in old than in young slow-twitch muscle. Even when some statistical comparisons of the total protein carbonyl levels would not reveal differences, principal component analysis (PCA) classified the carbonyl profiles into four distinct sample groups of different age and muscle types. In addition, PCA was used to predict that most age-related or muscle-type-related changes in carbonyl levels occur in proteins with a molecular weight between 9.8 and 11.7 kD.
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PMID:Principal component analysis reveals age-related and muscle-type-related differences in protein carbonyl profiles of muscle mitochondria. 1912 40


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