BIOMAT Database Logo BIOMAT Database Logo

The preparation and chemical properties of some glucuronyl esters of beta-glycyrrhetic acid (3 beta-hydroxy-11-oxo-olean-12-en-30-oic acid) and its derivatives. 1970

P Iveson, and D V Parke

UI MeSH Term Description Entries
D004952 Esters Compounds derived from organic or inorganic acids in which at least one hydroxyl group is replaced by an –O-alkyl or another organic group. They can be represented by the structure formula RCOOR’ and are usually formed by the reaction between an acid and an alcohol with elimination of water. Ester
D005965 Glucuronates Derivatives of GLUCURONIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that include the 6-carboxy glucose structure. Glucosiduronates,Glucuronic Acids,Acids, Glucuronic
D005988 Glyceric Acids Three-carbon SUGAR ACIDS with the formula HOCH2(CHOH)COOH. Acids, Glyceric
D006027 Glycosides Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed) Glycoside

Related Publications

P Iveson, and D V Parke
Triterpenoide. XIX. 3 beta-Hydroxy-11-oxo-18 alpha-olean-12-en-28-saure-methylester und 3,11-dioxo-18 alpha-olean-12-en-28-saure-methylester
April 2000, Acta crystallographica. Section C, Crystal structure communications,
P Iveson, and D V Parke
Synthesis and evaluation of nitrogen-containing derivatives of 3,11-dioxo-olean-12-en-30-oic acid against HIV-1 protease.
February 2024, Natural product research,
P Iveson, and D V Parke
Preparation of [3 alpha-3H]3 beta-hydroxy-18 beta- and 3 alpha-hydroxy-18(beta and alpha)-glycyrrhetic acid and radioimmunoassay of glycyrrhetic acid.
September 1988, Chemical & pharmaceutical bulletin,
P Iveson, and D V Parke
Propargylaminyl 3α-hy-droxy-11-oxo-18β-olean-12-en-29-oate.
November 2011, Acta crystallographica. Section E, Structure reports online,
P Iveson, and D V Parke
The preparation of some derivatives of glycyrrhetic acid and oleanolic acid.
October 1967, The Journal of pharmacy and pharmacology,
P Iveson, and D V Parke
Induction of laryngeal cancer cell death by Ent-11-hydroxy-15-oxo-kaur-16-en-19-oic acid.
November 2010, Head & neck,
P Iveson, and D V Parke
3alpha-hydroxy-5beta-chol-11 -en-24-oic acid, a new fungal metabolite.
January 1974, Journal of the Chemical Society. Perkin transactions 1,
P Iveson, and D V Parke
Spectrophotometric determination of lantadene A, 22 beta-angeloyloxy-3-oxoolean-12-en-28-oic acid.
February 1983, Analytical biochemistry,
P Iveson, and D V Parke
The preparation and properties of some beta-aminopropionic acid derivatives.
August 1946, Journal of the American Chemical Society,
P Iveson, and D V Parke
3-Cyano-11-oxo-3,4-seco-12a-aza-C-homoolean-4(23)-en-28-oic acid methyl ester.
February 2012, Acta crystallographica. Section E, Structure reports online,
Copied contents to your clipboard!