DERIVATIVES OF 6-AMINOPENICILLANIC ACID. V. SYNTHESIS OF 6-AMINOPENICILLANYL ALCOHOL AND CERTAIN DERIVATIVES. 1964

Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY

UI MeSH Term Description Entries
D010397 Penicillanic Acid A building block of penicillin, devoid of significant antibacterial activity. (From Merck Index, 11th ed) Acid, Penicillanic
D010406 Penicillins A group of antibiotics that contain 6-aminopenicillanic acid with a side chain attached to the 6-amino group. The penicillin nucleus is the chief structural requirement for biological activity. The side-chain structure determines many of the antibacterial and pharmacological characteristics. (Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p1065) Antibiotics, Penicillin,Penicillin,Penicillin Antibiotics
D010600 Pharmacology The study of the origin, nature, properties, and actions of drugs and their effects on living organisms. Pharmacologies
D012106 Research Critical and exhaustive investigation or experimentation, having for its aim the discovery of new facts and their correct interpretation, the revision of accepted conclusions, theories, or laws in the light of newly discovered facts, or the practical application of such new or revised conclusions, theories, or laws. (Webster, 3d ed) Research Priorities,Laboratory Research,Research Activities,Research and Development,Activities, Research,Activity, Research,Development and Research,Priorities, Research,Priority, Research,Research Activity,Research Priority,Research, Laboratory
D002626 Chemistry, Pharmaceutical Chemistry dealing with the composition and preparation of agents having PHARMACOLOGIC ACTIONS or diagnostic use. Medicinal Chemistry,Chemistry, Pharmaceutic,Pharmaceutic Chemistry,Pharmaceutical Chemistry,Chemistry, Medicinal
D000431 Ethanol A clear, colorless liquid rapidly absorbed from the gastrointestinal tract and distributed throughout the body. It has bactericidal activity and is used often as a topical disinfectant. It is widely used as a solvent and preservative in pharmaceutical preparations as well as serving as the primary ingredient in ALCOHOLIC BEVERAGES. Alcohol, Ethyl,Absolute Alcohol,Grain Alcohol,Alcohol, Absolute,Alcohol, Grain,Ethyl Alcohol
D000438 Alcohols Alkyl compounds containing a hydroxyl group. They are classified according to relation of the carbon atom: primary alcohols, R-CH2OH; secondary alcohols, R2-CHOH; tertiary alcohols, R3-COH. (From Grant & Hackh's Chemical Dictionary, 5th ed)
D013210 Staphylococcus A genus of gram-positive, facultatively anaerobic, coccoid bacteria. Its organisms occur singly, in pairs, and in tetrads and characteristically divide in more than one plane to form irregular clusters. Natural populations of Staphylococcus are found on the skin and mucous membranes of warm-blooded animals. Some species are opportunistic pathogens of humans and animals.

Related Publications

Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
May 1966, Chemistry & industry,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
January 1968, Antimicrobial agents and chemotherapy,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
November 1965, Journal of medicinal chemistry,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
March 1967, The Journal of antibiotics,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
August 1965, Yao xue xue bao = Acta pharmaceutica Sinica,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
January 1976, Polish journal of pharmacology and pharmacy,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
October 1965, Il Farmaco; edizione scientifica,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
July 1965, The Journal of antibiotics,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
August 1961, Proceedings of the Royal Society of London. Series B, Biological sciences,
Y G PERRON, and L B CRAST, and J M ESSERY, and R R FRASER, and J C GODFREY, and C T HOLDREGE, and W F MINOR, and M E NEUBERT, and R A PARTYKA, and L C CENEY
April 1968, The Journal of antibiotics,
Copied contents to your clipboard!