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Results: 1-9 |
Results: 9
CYTOTOXICITY OF A SERIES OF MONO-SUBSTITUTED AND DISUBSTITUTED THIOUREA IN FRESHLY ISOLATED RAT HEPATOCYTES - A PRELIMINARY STRUCTURE-TOXICITY RELATIONSHIP STUDY
Authors: ONDERWATER RCA COMMANDEUR JNM GROOT EJ SITTERS A MENGE WMPB VERMEULEN NPE
Citation: Rca. Onderwater et al., CYTOTOXICITY OF A SERIES OF MONO-SUBSTITUTED AND DISUBSTITUTED THIOUREA IN FRESHLY ISOLATED RAT HEPATOCYTES - A PRELIMINARY STRUCTURE-TOXICITY RELATIONSHIP STUDY, Toxicology, 125(2-3), 1998, pp. 117-129
NOVEL QUALITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS FOR THE ANTINOCICEPTIVE ACTIONS OF H-2 ANTAGONISTS, H-3 ANTAGONISTS AND DERIVATIVES
Authors: HOUGH LB NALWALK JW LI BY LEURS R MENGE WMPB TIMMERMAN H CARLILE ME COFFI C WENTLAND M
Citation: Lb. Hough et al., NOVEL QUALITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS FOR THE ANTINOCICEPTIVE ACTIONS OF H-2 ANTAGONISTS, H-3 ANTAGONISTS AND DERIVATIVES, The Journal of pharmacology and experimental therapeutics, 283(3), 1997, pp. 1534-1543
HISTAMINE HOMOLOGS DISCRIMINATING BETWEEN 2 FUNCTIONAL H-3 RECEPTOR ASSAYS - EVIDENCE FOR H-3 RECEPTOR HETEROGENEITY
Authors: LEURS R KATHMANN M VOLLINGA RC MENGE WMPB SCHLICKER E TIMMERMAN H
Citation: R. Leurs et al., HISTAMINE HOMOLOGS DISCRIMINATING BETWEEN 2 FUNCTIONAL H-3 RECEPTOR ASSAYS - EVIDENCE FOR H-3 RECEPTOR HETEROGENEITY, The Journal of pharmacology and experimental therapeutics, 276(3), 1996, pp. 1009-1015
SYNTHESIS OF NOVEL SE-SUBSTITUTED SELENOCYSTEINE DERIVATIVES AS POTENTIAL KIDNEY SELECTIVE PRODRUGS OF BIOLOGICALLY-ACTIVE SELENOL COMPOUNDS - EVALUATION OF KINETICS OF BETA-ELIMINATION REACTIONS IN RAT RENAL CYTOSOL
Authors: ANDREADOU I MENGE WMPB COMMANDEUR JNM WORTHINGTON EA VERMEULEN NPE
Citation: I. Andreadou et al., SYNTHESIS OF NOVEL SE-SUBSTITUTED SELENOCYSTEINE DERIVATIVES AS POTENTIAL KIDNEY SELECTIVE PRODRUGS OF BIOLOGICALLY-ACTIVE SELENOL COMPOUNDS - EVALUATION OF KINETICS OF BETA-ELIMINATION REACTIONS IN RAT RENAL CYTOSOL, Journal of medicinal chemistry, 39(10), 1996, pp. 2040-2046
HISTAMINE AS A MARKER FOR HYDROXYL RADICALS
Authors: CHING TL VANDERHEE RM BHOELAN NM BLAUW J MENGE WMPB DEJONG J BAST A
Citation: Tl. Ching et al., HISTAMINE AS A MARKER FOR HYDROXYL RADICALS, Mediators of inflammation, 4(5), 1995, pp. 339-343
SYNTHESIS AND IN-VITRO PHARMACOLOGY OF DIMAPRIT ANALOGS WITH HISTAMINE H-2-AGONISTIC AND H-1-ANTAGONISTIC ACTIVITIES
Authors: CHRISTIAANS JAM VANDERGOOT H MENGE WMPB TIMMERMAN H
Citation: Jam. Christiaans et al., SYNTHESIS AND IN-VITRO PHARMACOLOGY OF DIMAPRIT ANALOGS WITH HISTAMINE H-2-AGONISTIC AND H-1-ANTAGONISTIC ACTIVITIES, European journal of medicinal chemistry, 30(9), 1995, pp. 673-678
HOMOLOGS OF HISTAMINE AS HISTAMINE H-3 RECEPTOR ANTAGONISTS - A NEW POTENT AND SELECTIVE H-3 ANTAGONIST, 4(5)-(5-AMINOPENTYL)-1H-IMIDAZOLE
Authors: VOLLINGA RC MENGE WMPB LEURS R TIMMERMAN H
Citation: Rc. Vollinga et al., HOMOLOGS OF HISTAMINE AS HISTAMINE H-3 RECEPTOR ANTAGONISTS - A NEW POTENT AND SELECTIVE H-3 ANTAGONIST, 4(5)-(5-AMINOPENTYL)-1H-IMIDAZOLE, Journal of medicinal chemistry, 38(2), 1995, pp. 266-271
NEW ANALOGS OF BURIMAMIDE AS POTENT AND SELECTIVE HISTAMINE H-3 RECEPTOR ANTAGONISTS - THE EFFECT OF CHAIN-LENGTH VARIATION OF THE ALKYL SPACER AND MODIFICATIONS OF THE N-THIOUREA SUBSTITUENT
Authors: VOLLINGA RC MENGE WMPB LEURS R TIMMERMAN H
Citation: Rc. Vollinga et al., NEW ANALOGS OF BURIMAMIDE AS POTENT AND SELECTIVE HISTAMINE H-3 RECEPTOR ANTAGONISTS - THE EFFECT OF CHAIN-LENGTH VARIATION OF THE ALKYL SPACER AND MODIFICATIONS OF THE N-THIOUREA SUBSTITUENT, Journal of medicinal chemistry, 38(12), 1995, pp. 2244-2250
A NEW POTENT AND SELECTIVE HISTAMINE H-3 RECEPTOR AGONIST, 4-(1H-IMIDAZOL-4-YLMETHYL)PIPERIDINE
Authors: VOLLINGA RC DEKONING JP JANSEN FP LEURS R MENGE WMPB TIMMERMAN H
Citation: Rc. Vollinga et al., A NEW POTENT AND SELECTIVE HISTAMINE H-3 RECEPTOR AGONIST, 4-(1H-IMIDAZOL-4-YLMETHYL)PIPERIDINE, Journal of medicinal chemistry, 37(3), 1994, pp. 332-333
Risultati: 1-9 |