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Results: 1-15 |
Results: 15
Synthesis and pharmacological evaluation of imidazoline sites I-1 and I-2 selective ligands
Authors: Anastassiadou, M Danoun, S Crane, L Baziard-Mouysset, G Payard, M Caignard, DH Rettori, MC Renard, P
Citation: M. Anastassiadou et al., Synthesis and pharmacological evaluation of imidazoline sites I-1 and I-2 selective ligands, BIO MED CH, 9(3), 2001, pp. 585-592
Design, synthesis and antiproliferative activity of tripentones: A new series of antitubulin agents
Authors: Lisowski, V Enguehard, C Lancelot, JC Caignard, DH Lambel, S Leonce, S Pierre, A Atassi, G Renard, P Rault, S
Citation: V. Lisowski et al., Design, synthesis and antiproliferative activity of tripentones: A new series of antitubulin agents, BIOORG MED, 11(16), 2001, pp. 2205-2208
Novel antitumor artemisinin derivatives targeting G1 phase of the cell cycle
Authors: Li, Y Shan, F Wu, JM Wu, GS Ding, J Xiao, D Yang, WY Atassi, G Leonce, S Caignard, DH Renard, P
Citation: Y. Li et al., Novel antitumor artemisinin derivatives targeting G1 phase of the cell cycle, BIOORG MED, 11(1), 2001, pp. 5-8
Synthesis and cytotoxicity of artemisinin derivatives containing cyanoarylmethyl group
Authors: Wu, JM Shan, F Wu, GS Li, Y Ding, J Xiao, D Han, JX Atassi, G Leonce, S Caignard, DH Renard, P
Citation: Jm. Wu et al., Synthesis and cytotoxicity of artemisinin derivatives containing cyanoarylmethyl group, EUR J MED C, 36(5), 2001, pp. 469-479
Antitumor agents. Synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system
Authors: Capilla, AS Sanchez, I Caignard, DH Renard, P Pujol, MD
Citation: As. Capilla et al., Antitumor agents. Synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system, EUR J MED C, 36(4), 2001, pp. 389-393
Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents
Authors: Capilla, AS Romero, M Pujol, MD Caignard, DH Renard, P
Citation: As. Capilla et al., Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents, TETRAHEDRON, 57(39), 2001, pp. 8297-8303
Design and synthesis of some new pyranoxanthenones with cytotoxic activity
Authors: Ghirtis, K Pouli, N Marakos, P Skaltsounis, AL Leonce, S Atassi, G Caignard, DH
Citation: K. Ghirtis et al., Design and synthesis of some new pyranoxanthenones with cytotoxic activity, J HETERO CH, 38(1), 2001, pp. 147-152
Synthesis and conformational analysis of some new pyrano[2,3-c]xanthen-7-one and pyrano[3,2-b]xanthen-6-one derivatives with cytotoxic activity
Authors: Ghirtis, K Pouli, N Marakos, P Skaltsounis, AL Leonce, S Caignard, DH Atassi, G
Citation: K. Ghirtis et al., Synthesis and conformational analysis of some new pyrano[2,3-c]xanthen-7-one and pyrano[3,2-b]xanthen-6-one derivatives with cytotoxic activity, HETEROCYCLE, 53(1), 2000, pp. 93-106
Synthesis and structure-activity relationships of novel arylalkyl 4-benzylpiperazine derivatives as sigma site selective ligands
Authors: Younes, S Labssita, Y Baziard-Mouysset, G Payard, M Rettori, MC Renard, P Pfeiffer, B Caignard, DH
Citation: S. Younes et al., Synthesis and structure-activity relationships of novel arylalkyl 4-benzylpiperazine derivatives as sigma site selective ligands, EUR J MED C, 35(1), 2000, pp. 107-121
Synthesis and cytotoxic activity of 2-dialkylaminoethylamino substituted xanthenone and thioxanthenone derivatives
Authors: Kostakis, I Ghirtis, K Pouli, N Marakos, P Alexios-Leandros, S Leonce, S Caignard, DH Atassi, G
Citation: I. Kostakis et al., Synthesis and cytotoxic activity of 2-dialkylaminoethylamino substituted xanthenone and thioxanthenone derivatives, FARMACO, 55(6-7), 2000, pp. 455-460
Synthesis and pharmacological evaluation of novel 4-(4-fluorobenzoyl)piperidine derivatives as mixed 5-HT1A/5-HT2A/D-2 receptor ligands
Authors: Diouf, O Carato, P Lesieur, I Rettori, MC Caignard, DH
Citation: O. Diouf et al., Synthesis and pharmacological evaluation of novel 4-(4-fluorobenzoyl)piperidine derivatives as mixed 5-HT1A/5-HT2A/D-2 receptor ligands, EUR J MED C, 34(1), 1999, pp. 69-73
Semisynthesis and cytotoxicity of styryl-lactone derivatives
Authors: Bermejo, A Leonce, S Cabedo, N Andreu, I Caignard, DH Atassi, G Cortes, D
Citation: A. Bermejo et al., Semisynthesis and cytotoxicity of styryl-lactone derivatives, J NAT PROD, 62(8), 1999, pp. 1106-1109
Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation
Authors: Ansar, M Ebrik, S Mouhoub, R Vaccher, C Vaccher, MP Flouquet, N Bakkas, S Taoufik, J Debaert, M Caignard, DH Renard, P Berthelot, P
Citation: M. Ansar et al., Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation, THERAPIE, 54(5), 1999, pp. 651-658
6-aminoalkyloxazolo[4,5-b]pyridin-2(3H)-ones: Synthesis and evaluation of antinoceptive activity
Authors: Savelon, L Bizot-Espiard, JG Caignard, DH Pfeiffer, B Renard, P Viaud, MC Guillaumet, G
Citation: L. Savelon et al., 6-aminoalkyloxazolo[4,5-b]pyridin-2(3H)-ones: Synthesis and evaluation of antinoceptive activity, BIO MED CH, 6(11), 1998, pp. 1963-1973
Pyridothiadiazinedioxides structurally related to quinazolinones cholecystokinin gastrin receptor ligands: synthesis and biological evaluation
Authors: Pirotte, B de Tullio, P Podona, T Diouf, O Dewalque, D Neven, P Masereel, B Caignard, DH Renard, P Delarge, J
Citation: B. Pirotte et al., Pyridothiadiazinedioxides structurally related to quinazolinones cholecystokinin gastrin receptor ligands: synthesis and biological evaluation, EUR J PH SC, 7(1), 1998, pp. 29-40
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