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Chemical structure of carbamates. In organic chemistry, a carbamate is a category of organic compounds with the general formula R 2 NC(O)OR and structure >N−C(=O)−O−, which are formally derived from carbamic acid (NH 2 COOH).
American Chemical Society - biochemistry - chemistry - computer-assisted drug design - computational chemistry - dependent variable - environmental chemistry - experiment - geochemistry - hypothesis - independent variable - inorganic chemistry - law - matter - medicinal chemistry - organic chemistry - pharmacology - pharmacognosy - physical ...
Galenic formulation deals with the principles of preparing and compounding medicines in order to optimize their absorption.Galenic formulation is named after Claudius Galen, a 2nd Century AD Greek physician, who codified the preparation of drugs using multiple ingredients.
Medicinal or pharmaceutical chemistry is a scientific discipline at the intersection of chemistry and pharmacy involved with designing and developing pharmaceutical drugs. Medicinal chemistry involves the identification, synthesis and development of new chemical entities suitable for therapeutic use.
The 2H-1,2,3-triazole tautomer is the major form in aqueous solution. [6] It is a surprisingly stable structure compared to other organic compounds with three adjacent nitrogen atoms. However, flash vacuum pyrolysis at 500 °C leads to loss of molecular nitrogen (N 2) leaving a three-member aziridine ring.
Peptide therapeutics are peptides or polypeptides (oligomers or short polymers of amino acids) which are used to for the treatment of diseases.Naturally occurring peptides may serve as hormones, growth factors, neurotransmitters, ion channel ligands, and anti-infectives; peptide therapeutics mimic such functions.
A drug class is a group of medications and other compounds that share similar chemical structures, act through the same mechanism of action (i.e., binding to the same biological target), have similar modes of action, and/or are used to treat similar diseases.
Louis Pasteur - pioneering stereochemist. Chirality can be traced back to 1812, when physicist Jean-Baptiste Biot found out about a phenomenon called "optical activity." [10] Louis Pasteur, a famous student of Biot's, made a series of observations that led him to suggest that the optical activity of some substances is caused by their molecular asymmetry, which makes nonsuperimposable mirror ...