BIOMAT Database Logo BIOMAT Database Logo

Stereoselective metabolism of the enantiomers of hexobarbital. 1969

R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008297 Male Males
D008748 Methylcholanthrene A carcinogen that is often used in experimental cancer studies. 20-Methylcholanthrene,3-Methylcholanthrene,20 Methylcholanthrene,3 Methylcholanthrene
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D010634 Phenobarbital A barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. Phenemal,Phenobarbitone,Phenylbarbital,Gardenal,Hysteps,Luminal,Phenobarbital Sodium,Phenobarbital, Monosodium Salt,Phenylethylbarbituric Acid,Acid, Phenylethylbarbituric,Monosodium Salt Phenobarbital,Sodium, Phenobarbital
D011335 Proadifen An inhibitor of drug metabolism and CYTOCHROME P-450 ENZYME SYSTEM activity. Propyladiphenin,Diethylaminoethyldiphenylpropyl Acetate,Proadifen Hydrochloride,SK&F-525-A,SK-525A,SKF-525-A,SKF-525A,Acetate, Diethylaminoethyldiphenylpropyl,Hydrochloride, Proadifen,SK 525A,SK&F 525 A,SK&F525A,SK525A,SKF 525 A,SKF525A
D005260 Female Females
D006591 Hexobarbital A barbiturate that is effective as a hypnotic and sedative. Evipan,Hexenal,Hexobarbitone,Sodium Hexobarbital,Hexobarbital, Sodium
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D012737 Sex Factors Maleness or femaleness as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or effect of a circumstance. It is used with human or animal concepts but should be differentiated from SEX CHARACTERISTICS, anatomical or physiological manifestations of sex, and from SEX DISTRIBUTION, the number of males and females in given circumstances. Factor, Sex,Factors, Sex,Sex Factor

Related Publications

R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective hydroxylation of hexobarbital enantiomers by rat liver microsomes.
January 1980, Drug metabolism and disposition: the biological fate of chemicals,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Age-associated stereoselective alterations in hexobarbital metabolism.
April 1988, Clinical pharmacology and therapeutics,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective formation of glucuronides in metabolism of hexobarbital enantiomers in vivo: isolation and quantitation of glucuronides in rabbit urine.
January 1981, Drug metabolism and disposition: the biological fate of chemicals,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Disposition of hexobarbital enantiomers in the rat.
January 1983, Drug metabolism and disposition: the biological fate of chemicals,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Influence of age on stereoselective pharmacokinetics and metabolism of hexobarbital in the rat.
September 1992, Mechanisms of ageing and development,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective excretion and first-pass metabolism of clausenamide enantiomers.
July 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective metabolism of tetrahydropalmatine enantiomers in rat liver microsomes.
May 2012, Chirality,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective metabolism of halothane enantiomers to trifluoroacetylated liver proteins.
January 1995, Drug metabolism reviews,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective metabolism of bisoprolol enantiomers in dogs and humans.
January 1998, Life sciences,
R L Furner, and J S McCarthy, and R E Stitzel, and M W Anders
Stereoselective metabolism and pharmacokinetics of disopyramide enantiomers in humans.
January 1988, Drug metabolism and disposition: the biological fate of chemicals,
Copied contents to your clipboard!