Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: CAS:142-82-5 (heptane)
 3,094 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A number of 3-bromo-, 3-nitro-, and 3-ethoxycarbonyl-5,7-dialkylpyrazolo[1,5-a]pyrimidines were synthesized and screened as in vitro cAMP phosphodiesterase inhibitors. The condensation of 3-aminopyrazole with symmetrical beta-diketones (acetylacetone, heptane-3,5-dione, etc.) afforded symmetrical dialkylpyrazolo[1,5-a]pyrimidines (5). The reaction of 3-aminopyrazole with unsymmetrical beta-diketones (hexane-2,4-dione, heptane-3,5-dione, etc.) gave a mixture of 5-methyl-7-alkylpyrazolo[1,5-a]pyrimidine (3) and 5-alkyl-7-methylpyrazolo[1,5-a]pyrimidines (4). The technique for the separation of 3 from 4 is described. The inhibition constants, alpha (the ratio of the molar I50 of theophylline to the molar I50 of the test compounds), were subjected to a Hansch correlation analysis. The results indicated that PDE isolated from beef heart tissue was most sensitive to changes in the length of the alkyl group in the 5 position of the pyrazolo[1,5-a]pyrimidine ring, whereas the PDE isolated from rabbit lung tissue was more sensitive to changes in the length of the 7-alkyl group. Experimentally and theoretically, the n-propyl group was found to approximate the ideal size for the alkyl group in both the 5 and 7 positions;5,7-di-n-propyl-3-ethoxycarbonylpyrazolo[1,5-a]pyrimidine (5e) was the most potent inhibitor of both lung and heart PDE.
 ...
PMID:Adenosine cyclic 3',5',-monophosphate phosphodiesterasr inhibitors. 2.3-Substituted 5,7-dialkylpyrazolo [1,5-a]pyrimidines. 16 80

The results of the determination of oil content depend on the method and on the solvent used. Extractions by the Twisselmann method give increasing yields in the order n-pentane, hexane, and n-heptane. Using the Soxhlet extraction, much lower yields were obtained with n-heptane than with the other two solvents. In both methods, the phospholipid content in the extracts depends only on the solvent and not on the method used. The yield and composition of the mixture of phospholipids vary in the different methods of extraction.
 ...
PMID:[Solubility of phospholipids in oilseeds depending on the extraction conditions (author's transl)]. 70 8

Temporal and voltage-induced changes of reflectivity (R), the optical phase difference in transmitted polarized light, of tension and total capacity of bilayer lipid membrane (BLM) were studied. The membranes were mainly formed from total brain phospholipids (TP) in n-alkanes. 1) Reflectivity of "black" regions of films made of TP in decane and hexadecane decreases by several percent with a time constant (tauR) of about 30 min, whereas that of membranes with hexane and heptane does not depend on time (with an accuracy up to 1--2%). The BLM tension decreases appreciably in the course of time and reaches its steady-state value in tens of minutes after complete blackening of the membrane. 2) Under prolonged (up to tens of minutes) action of voltage (V) no R changes of BLMs with hexane, heptane, and hexadecane were revealed at a noise level of 0.2%. Blms with decane usually respond to voltage application, first by a rapid (jump-like) and then by a slow decrease of R with a value spread from 0.2% to 3%. 3) With higher amplitude and temporal resolutions of the signal (signal averaging method) it can be seen that after voltage jump R decreases down to a new steady-state value: at V = 100 mV, deltaR/R = -(2--4) . 10(-4) and tauR approximately 0.1 msec for BLMs from TP in heptane, and deltaR/R = -(3--6) . 10(-2) and tauR approximately 2 msec for BLMs from oxidized cholesterol in decane. It is shown in the latter case that the great value of deltaR/R is due to the contribution of invisible microlenses. In all the cases deltaR approximately V2. 4) It is concluded that at voltage jump a bilayer first becomes thinner due to volumic compression of its hydrocarbon core; then it spreads with a time constant of the order of 0.1 msec, getting thinner until a new equilibrium state is reached. Complete change of bilayer thickness is detah/h approximately -10(-4) at 100 mV.
 ...
PMID:Voltage-induced reflectivity relaxation of bilayer lipid membranes: on changes of bilayer thickness. 71 12

High-pressure liquid chromatographic (HPLC) systems were developed to separate quantitatively delta 9-tetrahydrocannabinol from heptane-extractable lipoidal and other endogenous substances in biological fluids. These substances interfered with the quantitation by flame-ionization GLC of the unmodified compound and by electron-capture GLC of the pentafluorobenzoyl derivative. Reversed-phase HPLC elution, with 47% acetonitrile in water, and normal-phase HPLC with 25% chloroform in heptane separated delta 9-tetrahydrocannabinol from 11-hydroxy-delta 9-tetrahydrocannabinol and other monohydroxylated tetrahydrocannabinols. These systems also purified stock solutions of delta 9-tetrahydrocannabinol from accompanying contaminants. The various monohydroxylated tetrahydrocannabinols were resolved from each other in the normal phase, 80% chloroform in heptane. The delta 8- and delta 9-tetrahydrocannabinols were separable in the normal phase with 5% tetrahydrofuran in hexane. The GLC analysis of pentafluorobenzoylated delta 9-tetrahydrocannabinol had a sensitivity of 1 ng/ml of plasma, with an estimated 5% standard error with the developed extraction and GLC procedures. Radiochemical analysis of the HPLC-separated fraction had a sensitivity of 0.2 ng/ml of plasma, with an estimated 2% standard error. There was no significant difference between the liquid scintillation and electron-capture GLC assays of the HPLC-separated delta 9-tetrahydrocannabinol obtained from the plasma of dogs administered the drug. Radiolabeled compounds can be added to plasma samples as internal standards to determine the recovery efficiencies of the several procedures in the analysis of unlabeled tetrahydrocannabinol.
 ...
PMID:Separation and analysis of delta 9-tetrahydrocannabinol in biological fluids by high-pressure liquid chromatography and GLC. 83 37

The dissolution of a solid immersed in a solvent was considered as a consecutive process, consisting of a primary surface interaction leading to the production of a new surface at the solid-liquid interface, solvation of the solid at the interface, and transfer of the solvated solid into the bulk of the solution. The energy changes involved in each step were studied for the dissolution of m-tolylacetamide in hexane and heptane. An energy diagram was constructed according to the proposed dissolution mechanism. The heats of dissolution determined from the energy diagram agreed well with those obtained experimentally.
 ...
PMID:Determination of energy change associated with dissolution of a solid. 88 59

Experiments were carried out to use thin-layer chromatography to determine pure substances of the organic phosphorous insecticides forat and phenothion. Three sorbents were employed to establish the most appropriate conditions for the application of a fast, readily applicably and highly sensitive method--silica gel G, DG and Kiselgur "Merk", as well as 14 mobile phases--monocompound (n-hexane, n-heptane, acetone benzol and toluol), double combinations (hexane-acetone 4:1, hexane-acetone 9:1, hexane-benzol 1:1, hexane-benzol 4:1, heptane-acetone 7:1, benzol-hexane 4:1, benzol-acetone 9:1, and petrolium ether-tetrachlormethane) and triple combinations (acetone-toluol-hexane 1:15 and 5 developers (a diazosalt, bromine vapours + diazosalt, palladium bichloride, bromphenol blue, and silver nitrate, sodium hydroxide, ammonia gas). Established was the fact that the best results are obtained with the use of silica gel G, the mobile phase heptan-acetone 7:1, and the developer of 0.2% solution of palladium bichloride in 0.5 per cent solution of hydrochloric acid. In chromatogrammes the forat compound appears as a tile red portion with a darker peripheral part and Rf = 0.61, and phenothion--in yellow, with a brownish halo and Rf = 0.41. The method is highly sensitive--for forat 0.5 microgram, and for phenothion 0.5 microgram. In determining these insecticides it is possible to use as a sorbent silica gel "Merk" 1:1 with the same degree of sensitivity, but with higher Rf values.
 ...
PMID:[Comparative thin-layer chromatographic studies for determining phorate and fenthion]. 90 7

HPLC systems were developed to permit quantitative separation of delta9-tetrahydrocannabinol from many of the heptane extractable lipoidal and other endogenous substances in biological fluids. These substances interfered with the quantification by flame ionization GLC of unmodified compound and by electron capture GLC of pentafluorobenzoylated compound. Reverse phase HPLC elution, with 47% acetonitrile in water, and normal phase HPLC with 25% chloroform in heptane, separated tetrahydrocannabinol from 11-hydroxy-delta9-tetrahydrocannabinol and other monohydroxylated tetrahydrocannabinols. These systems also purified stock solutions of tetrahydrocannabinol from accompanying contaminants. The various monohydroxylated tetrahydrocannabinols were resolved from each other in normal phase, 80% chloroform in heptane. The delta8 and delta9-tetrahydrocannabinols were separable in normal phase with 5% tetrahydrofuran in hexane. The GLC analysis of pentafluorobenzoylated tetrahydrocannabinol had a sensitivity of 1 ng/ml of plasma with an estimated 5% standard error of an assay with the extraction and GLC procedures given herein. Radiochemical analysis of the HPLC separated fraction had s sensitivity of 0.2 ng/ml of plasma with an estimated 2% standard error of an assay. There was no significant difference between the liquid scintillation and electron capture GLC assays of the HPLC separated delta9-tetrahydrocannabinol obtained from the plasma of dogs administered the drug. Radiolabelled compounds can be added to plasma samples as internal standards to determine the recovery efficiencies of the several procedures in the analysis of unlabelled tetrahydrocannabinol.
 ...
PMID:Separation and sensitive assay of THC in biological fluids by HPLC and GLC. 96 39

Glucose transport in Cladosporium resinae was studies with the aid of the non-metabolizable glucose analogue 3-O-methyl-D-glucose (3-O-MG). 3-O-MG, transported as a free sugar without phosphorylation, was found to inhibit glucose uptake competitively. Conversely, glucose was a competitive inhibitor of 3-O-MG uptake. Moreover, both glucose and 3-O-MG were able to bring about rapid counterflow intracellular 3-O-MG. Thus, glucose and 3-O-MG share the same entry and exit systems. The transport of 3-O-MG is carrier mediated and energy dependent as shown by saturation kinetics, strong temperature dependence, accumulation of unaltered 3-O-MG against a concentration gradient, and inhibition of uptake by NaN3, NaCN, and 2,4-dinitrophenol. The glucose transport system appeared to be constitutive for glucose transport in cells grown on fructose, galactose, mannose, xylose, or glucose. There was no derepressible low-Km glucose transport system in C. resinae. n-Hexane and n-heptane were found to inhibit 3-O-MG uptake rapidly at temperatures above 20 C. Over 50% inhibition of the uptake rate occurred after only 10 min of incubation with n-hexane at 30 C. The percentage of inhibition in the presence of n-hexane, compared to controls in the absence of n-hexane, was found to increase with increasing temperature. Longer-chain n-alkanes (C8 to C18) had no significant effect on uptake. The efflux of intracellular 3-O-MG, which appeared to occur by facilitated diffusion, was not affected by any of the n-alkanes tested including n-hexane.
 ...
PMID:Glucose transport and its inhibition by short-chain n-alkanes in Cladosporium resinae. 117 Oct 91

The antidote efficacy of liquid paraffin in oral solvent intoxications was investigated in dogs. Groups of 3 to 4 animals each received 1 ml/kg of methylchloroform, 0.3 ml/kg of benzene, or 3 ml/kg of a synthetic gasoline mixture (hexane/heptane/octane, ratio 30:50:20) by gastric intubation. After a prolonged interval the same animals were given 5 ml/kg of liquid paraffin by a separate tube in addition to one of the above solvents. The solvent concentrations in the blood were determined by gas chromatography at appropriate intervals. Administration of liquid paraffin in conjunction with methylchloroform does not significantly affect the absorption process. In the case of benzene and the synthetic gasoline mixture, however, liquid paraffin produces a distinct reduction in the rate of absorption. It is thus concluded that in the therapy of oral solvent-intoxication, liquid paraffin exhibits favorable antidote properties which may however differ from one solvent to the other. In clinically relevant situations involving coadministration of purgatives, the antidote effect must be assessed as being of a higher order than in our animal experiments in which purgatives had to be omitted for external reasons.
 ...
PMID:Antidote effect of liquid paraffin in oral solvent intoxication. 117 55

A gas chromatographic-mass spectrometric method is described for the determination of plasma selegiline. Tetradeuteroselegiline was synthesized and served as the internal standard. Human plasma samples (1 ml) containing 1-6 ng of selegiline were acidified, washed with diethyl ether-hexane, then alkalinized and extracted with heptane-isoamyl alcohol. Analytical separations were performed on a dimethylsilicone capillary column. Detection was by selected ion monitoring of the electron impact generated m/z 96 and 100 alpha-cleavage fragments of drug and internal standard, respectively.
 ...
PMID:Gas chromatographic-mass spectrometric determination of plasma selegiline using a deuterated internal standard. 147 90


1 2 3 4 5 6 7 8 9 10 Next >>