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Results: 1-7 |
Results: 7
SYNTHETIC MODIFICATIONS OF ASCOMYCIN .2. A SIMPLE AND EFFICIENT WAY TO MODIFIED ISO-ASCOMYCIN DERIVATIVES
Authors: ZIMMER R GRASSBERGER MA BAUMANN K HORVATH A SCHULZ G HAIDL E
Citation: R. Zimmer et al., SYNTHETIC MODIFICATIONS OF ASCOMYCIN .2. A SIMPLE AND EFFICIENT WAY TO MODIFIED ISO-ASCOMYCIN DERIVATIVES, Tetrahedron letters, 36(42), 1995, pp. 7635-7638
SYNTHESIS AND OXIDATIVE CLEAVAGE OF THE MAJOR EQUILIBRIUM PRODUCTS OFASCOMYCIN AND FK-506
Authors: BAUMANN K OBERHAUSER B GRASSBERGER MA HAIDL G SCHULZ G
Citation: K. Baumann et al., SYNTHESIS AND OXIDATIVE CLEAVAGE OF THE MAJOR EQUILIBRIUM PRODUCTS OFASCOMYCIN AND FK-506, Tetrahedron letters, 36(13), 1995, pp. 2231-2234
SYNTHETIC MODIFICATIONS OF ASCOMYCIN-I - A CHEMOSELECTIVE REMOVAL OF THE CYCLOHEXYL RESIDUE OF ASCOMYCIN
Authors: ZIMMER R GRASSBERGER MA BAUMANN K SCHULZ G HAIDL E
Citation: R. Zimmer et al., SYNTHETIC MODIFICATIONS OF ASCOMYCIN-I - A CHEMOSELECTIVE REMOVAL OF THE CYCLOHEXYL RESIDUE OF ASCOMYCIN, Tetrahedron, 50(48), 1994, pp. 13655-13670
DERIVATIVES OF A NOVEL CYCLOPEPTOLIDE .1. SYNTHESIS, ANTIFUNGAL ACTIVITY, AND STRUCTURE-ACTIVITY-RELATIONSHIPS
Authors: EMMER G GRASSBERGER MA MEINGASSNER JG SCHULZ G SCHAUDE M
Citation: G. Emmer et al., DERIVATIVES OF A NOVEL CYCLOPEPTOLIDE .1. SYNTHESIS, ANTIFUNGAL ACTIVITY, AND STRUCTURE-ACTIVITY-RELATIONSHIPS, Journal of medicinal chemistry, 37(13), 1994, pp. 1908-1917
DERIVATIVES OF A NOVEL CYCLOPEPTOLIDE .2. SYNTHESIS, ACTIVITY AGAINSTMULTIDRUG-RESISTANCE IN CHO AND KB CELLS IN-VITRO, AND STRUCTURE-ACTIVITY-RELATIONSHIPS
Authors: EMMER G GRASSBERGER MA SCHULZ G BOESCH D GAVERIAUX C LOOR F
Citation: G. Emmer et al., DERIVATIVES OF A NOVEL CYCLOPEPTOLIDE .2. SYNTHESIS, ACTIVITY AGAINSTMULTIDRUG-RESISTANCE IN CHO AND KB CELLS IN-VITRO, AND STRUCTURE-ACTIVITY-RELATIONSHIPS, Journal of medicinal chemistry, 37(13), 1994, pp. 1918-1928
REVERSION OF THE P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCE OF CANCER-CELLS BY FK-506 DERIVATIVES
Authors: JACHEZ B BOESCH D GRASSBERGER MA LOOR F
Citation: B. Jachez et al., REVERSION OF THE P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCE OF CANCER-CELLS BY FK-506 DERIVATIVES, Anti-cancer drugs, 4(2), 1993, pp. 223-229
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PHENYL-SUBSTITUTED BENZYLAMINE ANTIMYCOTICS - A NOVEL BENZYLBENZYLAMINE ANTIFUNGAL AGENT FOR SYSTEMIC TREATMENT
Authors: NUSSBAUMER P DORFSTATTER G GRASSBERGER MA LEITNER I MEINGASSNER JG THIRRING K STUTZ A
Citation: P. Nussbaumer et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF PHENYL-SUBSTITUTED BENZYLAMINE ANTIMYCOTICS - A NOVEL BENZYLBENZYLAMINE ANTIFUNGAL AGENT FOR SYSTEMIC TREATMENT, Journal of medicinal chemistry, 36(15), 1993, pp. 2115-2120
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