Authors:
Schmidtke, M
Schnittler, U
Jahn, B
Dahse, HM
Stelzner, A
Citation: M. Schmidtke et al., A rapid assay for evaluation of antiviral activity against coxsackie virusB3, influenza virus A, and herpes simplex virus type 1, J VIROL MET, 95(1-2), 2001, pp. 133-143
Authors:
Kleinwachter, P
Anh, N
Kiet, TT
Schlegel, B
Dahse, HM
Hartl, A
Grafe, U
Citation: P. Kleinwachter et al., Colossolactones, new triterpenoid metabolites from a Vietnamese mushroom Ganoderma colossum, J NAT PROD, 64(2), 2001, pp. 236-239
Citation: Hm. Dahse et al., Differentiation between inducers of apoptosis and nonspecific cytotoxic drugs by means of cell analyzer and immunoassay, PHARMAZIE, 56(6), 2001, pp. 489-491
Citation: P. Wissner et al., Structure activity relationship of antiproliferative N-acyl-aspartic acid dimethyl ester. 2. Variation of the aspartyl moiety, PHARMAZIE, 56(1), 2001, pp. 33-35
Authors:
Sakowski, J
Bohm, M
Sattler, I
Dahse, HM
Schlitzer, M
Citation: J. Sakowski et al., Synthesis, molecular modeling, and structure-activity relationship of benzophenone-based CAAX-peptidomimetic farnesyltransferase inhibitors, J MED CHEM, 44(18), 2001, pp. 2886-2899
Authors:
Fernekorn, U
Heinze, T
Schlegel, B
Dahse, HM
Grafe, U
Citation: U. Fernekorn et al., Synthesis of a new polycyclic quinone by reduction of a dihydrobenzo[a]naphthacenequinone, J ANTIBIOT, 54(2), 2001, pp. 191-192
Authors:
Schlitzer, M
Bohm, M
Sattler, I
Dahse, HM
Citation: M. Schlitzer et al., Design, synthesis and early structure-activity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate, BIO MED CH, 8(8), 2000, pp. 1991-2006
Citation: M. Schlitzer et Hm. Dahse, Structure activity relationship of antiproliferative N-acyl-beta-alanine amides, ANTICANC R, 20(6B), 2000, pp. 4431-4434
Authors:
Degenkolb, T
Heinze, S
Schlegel, B
Dornberger, K
Mollmann, U
Dahse, HM
Grafe, U
Citation: T. Degenkolb et al., Roseoferin, a new aminolipopeptide antibiotic complex from Mycogone rosea DSM 12973, structures and biological activities, J ANTIBIOT, 53(2), 2000, pp. 184-190
Citation: M. Schlitzer et al., Synthesis and evaluation of homofarnesoyl-substituted CAAX-peptidomimeticsas farnesyltransferase inhibitors and antiproliferative agents, BIO MED CH, 7(9), 1999, pp. 2037-2045
Citation: M. Schlitzer et al., Different amino acid replacements in CAAX-tetrapeptide based peptidomimetic farnesyltransferase inhibitors, ARCH PHARM, 332(4), 1999, pp. 124-132
Citation: M. Schlitzer et al., Synthesis and antiproliferative activity of N-acylaspartic acid dimethyl esters, ANTICANC R, 19(3A), 1999, pp. 2117-2120
Authors:
Ritzau, M
Heinze, S
Fleck, WF
Dahse, HM
Grafe, U
Citation: M. Ritzau et al., New macrodiolide antibiotics, 11-O-monomethyl- and 11,11 '-O-dimethylelaiophylins, from Streptomyces sp. HKI-0113 and HKI-0114, J NAT PROD, 61(11), 1998, pp. 1337-1339