Angehrn P - Search Results

1

Orally active 2-(alkyloxycarbonyl)-2-alkylideneethyl esters of cephalosporins.

Hubschwerlen C, Charnas R, Angehrn P, Furlenmeier A, Graser T, Montavon M. Hubschwerlen C, et al. Among authors: angehrn p. J Antibiot (Tokyo). 1992 Aug;45(8):1358-64. doi: 10.7164/antibiotics.45.1358. J Antibiot (Tokyo). 1992. PMID: 1399857 Free article.

2

Antibacterial properties of Ro 40-6890, a broad-spectrum cephalosporin, and its novel orally absorbable ester, Ro 41-3399.

Angehrn P, Hohl P, Hubschwerlen C, Page M, Then R. Angehrn P, et al. Antimicrob Agents Chemother. 1992 Dec;36(12):2825-34. doi: 10.1128/AAC.36.12.2825. Antimicrob Agents Chemother. 1992. PMID: 1482153 Free PMC article.

3

Synthesis and structure-activity relationship of (lactamylvinyl)cephalosporins exhibiting activity against staphylococci, pneumococci, and enterococci.

Heinze-Krauss I, Angehrn P, Guerry P, Hebeisen P, Hubschwerlen C, Kompis I, Page MG, Richter HG, Runtz V, Stalder H, Weiss U, Wei CC. Heinze-Krauss I, et al. Among authors: angehrn p. J Med Chem. 1996 Apr 26;39(9):1864-71. doi: 10.1021/jm950886v. J Med Chem. 1996. PMID: 8627610

4

Structure-based design of beta-lactamase inhibitors. 1. Synthesis and evaluation of bridged monobactams.

Heinze-Krauss I, Angehrn P, Charnas RL, Gubernator K, Gutknecht EM, Hubschwerlen C, Kania M, Oefner C, Page MG, Sogabe S, Specklin JL, Winkler F. Heinze-Krauss I, et al. Among authors: angehrn p. J Med Chem. 1998 Oct 8;41(21):3961-71. doi: 10.1021/jm980023c. J Med Chem. 1998. PMID: 9767633

5

Pyrimido[1,6-a]benzimidazoles: a new class of DNA gyrase inhibitors.

Hubschwerlen C, Pflieger P, Specklin JL, Gubernator K, Gmünder H, Angehrn P, Kompis I. Hubschwerlen C, et al. Among authors: angehrn p. J Med Chem. 1992 Apr 17;35(8):1385-92. doi: 10.1021/jm00086a006. J Med Chem. 1992. PMID: 1315393

6

Ro 13-9904/001, a novel potent and long-acting parenteral cephalosporin.

Reiner R, Weiss U, Brombacher U, Lanz P, Montavon M, Furlenmeier A, Angehrn P, Probst PJ. Reiner R, et al. Among authors: angehrn p. J Antibiot (Tokyo). 1980 Jul;33(7):783-6. doi: 10.7164/antibiotics.33.783. J Antibiot (Tokyo). 1980. PMID: 6967869 Free article.

7

Structure-based design of beta-lactamase inhibitors. 2. Synthesis and evaluation of bridged sulfactams and oxamazins.

Hubschwerlen C, Angehrn P, Gubernator K, Page MG, Specklin JL. Hubschwerlen C, et al. Among authors: angehrn p. J Med Chem. 1998 Oct 8;41(21):3972-5. doi: 10.1021/jm9800245. J Med Chem. 1998. PMID: 9767634

8

Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases.

Richter HG, Angehrn P, Hubschwerlen C, Kania M, Page MG, Specklin JL, Winkler FK. Richter HG, et al. Among authors: angehrn p. J Med Chem. 1996 Sep 13;39(19):3712-22. doi: 10.1021/jm9601967. J Med Chem. 1996. PMID: 8809160

9

(6R)-6-(substituted methyl)penicillanic acid sulfones: new potent beta-lactamase inhibitors.

Adam S, Then R, Angehrn P. Adam S, et al. Among authors: angehrn p. J Antibiot (Tokyo). 1993 Apr;46(4):641-6. doi: 10.7164/antibiotics.46.641. J Antibiot (Tokyo). 1993. PMID: 8388871 Free article.

10

Potential prodrugs of 6-acetylmethylenepenicillanic acid (Ro 15-1903).

Adam S, Then R, Angehrn P. Adam S, et al. Among authors: angehrn p. J Antibiot (Tokyo). 1986 Jun;39(6):833-8. doi: 10.7164/antibiotics.39.833. J Antibiot (Tokyo). 1986. PMID: 3015853 Free article.

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