Results 171 to 180 of about 7,278 (228)

Impact of loading dose β-lactam therapy on outcomes of KPC-producing Klebsiella pneumoniae bloodstream infections in non-ICU patients: a real world study. [PDF]

J Antimicrob Chemother
Frallonardo L, Guido G, De Gennaro N, De Iaco G, Signorile F, Cibelli M, De Luca A, Ritacco AI, Stolfa S, Di Gennaro F, Saracino A.   +10 more
europepmc   +1 more source

医薬品化学薬化学研究室 [PDF]

, 1997
小泉 徹, 斎藤 慎一, 武田 敬
core   +3 more sources

STOUT V2.0: SMILES to IUPAC name conversion using transformer models. [PDF]

J Cheminform
Rajan K, Zielesny A, Steinbeck C.
europepmc   +1 more source

Ceftazidime-Avibactam Pharmacokinetic Comparative In Vivo/In Vitro Study in a Critically Ill Children Under High-Volume Continuous Venovenous Hemodiafiltration. [PDF]

Pharmacol Res Perspect
Thy M, Debs A, Lui G, Froelicher-Bournaud L, Tréluyer JM, Oualha M.   +5 more
europepmc   +1 more source

[Studies on 1-azabicyclo compounds. IX. Condensation reaction of 3,4,6,7,8,9-hexahydro-2H-quinolizine with RNH 2 derivatives].

Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 1972
Y, Arata, S, Yoshifuji, T, Shioda
openaire   +1 more source

High-dose aztreonam potentiates the combined antimicrobial activity of ceftazidime-avibactam against extensively drug-resistant New Delhi metallo-β-lactamase positive <i>Pseudomonas aeruginosa</i> in severe pneumonia treatment: the first global case report. [PDF]

Front Cell Infect Microbiol
Liu Y, Mo C, Li M.
europepmc   +1 more source

New compounds: Preparation of Oxime Esters from 1-Azabicyclo[4.4.0]decane-4-one

Journal of Pharmaceutical Sciences, 1971
The synthesis of two new oxime esters is described. Preliminary results of pharmacological tests are also reported.
R. V. SAENZ, R. A. CROCHET
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Azabicyclo[3.1.0]hexane-1-ols as frameworks for the asymmetric synthesis of biologically active compounds

Tetrahedron Letters, 2007
Azabicyclo[3.1.0]hexane-1-ols, easily obtained by Ti(IV)-mediated cyclopropanation of amino acid derivatives, constitute versatile, and unprecedented intermediates for the asymmetric synthesis of pharmacologically active products. Indeed, through selective rearrangement, these compounds undergo unusual ring cleavage to lead to pyrrolidinones.
Mouhamad Jida, Régis Guillot, Jean Ollivier   +2 more
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ChemInform Abstract: STUDIES ON 1‐AZABICYCLO COMPOUNDS. XXVIII. SYNTHESIS OF 1‐METHYL‐PERHYDROAZOCIN‐5‐ONE FROM PYRROLIZIDINE

Chemischer Informationsdienst, 1979
AbstractDas aus (I) zugängliche N‐Oxid (II) ergibt mit Eisen(III)‐ nitrat/Weinsäure beim Erhitzen das Dehydropyrrolizidin (III), das auch durch Cyclisierung von (IV) und anschließende Spaltung von (V) über (VI) zugänglich ist.
Yoshio Arata, K. TANAKA, S. YOSHIFUJI, S. KANATOMO   +3 more
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Intramolecular, Metallacyclic Organoaluminium, ‐gallium and ‐indium Addition Compounds Crystal Structure of 1‐Galla‐5‐azabicyclo[3.3.3]undecane

Chemische Berichte, 1991
AbstractIntramolecularly base‐stabilized four‐coordinated metallacyclic organoaluminium, ‐gallium, and ‐indium compounds C5H10‐Al(CH2)3NMe2 (4), C4H8Ga(CH2)3NMe2 (5), C5H10Ga(CH2)3N‐Me2 (6), C5H10GaCH2CH(Me)CH2NMe2 (7), C4H8Ga(CH2)4NMe2 (8), C5H10Ga(CH2)4NMe2 (9), EtAl[(CH2)3]2NMe (10), MeGa‐[(CH2)3]2NMe (11), EtGa[(CH2)3]2NMe (12), MeIn[(CH2)3]2NMe ...
Herbert Schuman, Uwe Hartman, Wilfried Wassermann, Oliver Just, Andreas Dietrich, Ludwig Pohl, M. Hostalek, M. Lokai   +7 more
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