- Synthesis, kinase inhibitory potencies and in vitro antiproliferative activity of isoindigo and 7 '-azaisoindigo derivatives substituted by Sonogashira cross-coupling
[作者:Bouchikhi, F; Anizon, F; Moreau, P,期刊:European Journal of Medicinal Chemistry, 页码:2705-2710 , 文章类型: Article,,卷期:2009年44-6]
- In the course of structure-activity relationship studies we were interested in the synthesis of isoindigo and 7'-azaisoindigo derivatives substituted at the N-1 position by a 1-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos...
- Antitumour activity of novel 1,10-phenanthroline and 5-amino-1,10-phenanthroline derivatives
[作者:Wesselinova, D; Neykov, M; Kaloyanov, N; Toshkova, R; Dimitrov, G,期刊:European Journal of Medicinal Chemistry, 页码:2720-2723 , 文章类型: Article,,卷期:2009年44-6]
- Synthesis and impact on the tumour growth of palladium(II) complex of 5-amino-1,10-phenanthroline Pd(5-NH2-phen)(2)(NO3)(2) and the protonated dimer (phen)(2)(H+)(BF4-) have been described. In the reported experiments a ...
- Structure-activity relationships for dipeptide prodrugs of acyclovir: Implications for prodrug design
[作者:Santos, CR; Capela, R; Pereira, CSGP; Valente, E; Gouveia, L; Pannecouque, C; De Clercq, E; Moreira, R; Gomes, P,期刊:European Journal of Medicinal Chemistry, 页码:2339-2346 , 文章类型: Article,,卷期:2009年44-6]
- A series of water-soluble dipeptide ester prodrugs of the antiviral acyclovir (ACV) were evaluated for their chemical stability, cytotoxicity, and antiviral activity against several strains of Herpes Simplex-1 and -2, va...
- Synthesis, antimicrobial and antiviral evaluation of substituted imidazole derivatives
[作者:Sharma, D; Narasimhan, B; Kumar, P; Judge, V; Narang, R; De Clercq, E; Balzarini, J,期刊:European Journal of Medicinal Chemistry, 页码:2347-2353 , 文章类型: Article,,卷期:2009年44-6]
- In the present study, we have synthesized 2-(substituted phenyl)-1H-imidazole (1-12) and (substituted phenyl)-[2-(substituted phenyl)-imidazol-1-yl]-methanone (13-26) analogues and screened them for their antimicrobial a...
- Classification models for CYP450 3A4 inhibitors and non-inhibitors
[作者:Choi, I; Kim, SY; Kim, H; Kang, NS; Bae, MA; Yoo, SE; Jung, J; No, KT,期刊:European Journal of Medicinal Chemistry, 页码:2354-2360 , 文章类型: Article,,卷期:2009年44-6]
- Cytochrome P450 3A4 (CYP3A4) is the predominant enzyme involved in the oxidative metabolic pathways of many drugs. The inhibition of this enzyme in many cases leads to an undesired accumulation of the administered therap...
- Synthesis and antioxidant potential of novel synthetic benzophenone analogues
[作者:Tzanova, T; Gerova, M; Petrov, O; Karaivanova, M; Bagrel, D,期刊:European Journal of Medicinal Chemistry, 页码:2724-2730 , 文章类型: Article,,卷期:2009年44-6]
- Considering that oxidative stress is strongly implicated in the toxicity of chemotherapy, much effort is focused on the research of diverse antioxidants as protective agents. An efficient synthesis of three novel benzoph...
- New antimalarial and cytotoxic 4-nerolidylcatechol derivatives
[作者:Pinto, ACD; Silva, LFR; Cavalcanti, BC; Melo, MRS; Chaves, FCM; Lotufo, LVC; de Moraes, MO; de Andrade-Neto, VF; Tadei, WP; Pessoa, CO; Vieira, PPR; Pohlit, AM,期刊:European Journal of Medicinal Chemistry, 页码:2731-2735 , 文章类型: Article,,卷期:2009年44-6]
- 4-Nerolidylcatechol (1) was isolated from cultivated Pothomorphe peltata root on a multigram scale using straight-forward solvent extraction-column chromatography. New semi-synthetic derivatives of I were prepared and te...
- The preparation and in vitro antiproliferative activity of phthalimide based ketones on MDAMB-231 and SKHep-1 human carcinoma cell lines
[作者:Chan, SH; Lam, KH; Chui, CH; Gambari, R; Yuen, MCW; Wong, RSM; Cheng, GYM; Lau, FY; Au, YK; Cheng, CH; Lai, PBS; Kan, CW; Kok, SHL; Tang, JCO; Chan, ASC,期刊:European Journal of Medicinal Chemistry, 页码:2736-2740 , 文章类型: Article,,卷期:2009年44-6]
- The 'one pot' condensation reaction for the synthesis and potent anti proliferative inhibition of alpha-phthalimide based ketones is reported here. 2-Phthalimide-1-(4-fluoro-phenyl)ethanone (5) showed the best growth inh...
- Aroylpropionic acid based 2,5-disubstituted-1,3,4-oxadiazoles: Synthesis and their anti-inflammatory and analgesic activities
[作者:Akhter, M; Husain, A; Azad, B; Ajmal, M,期刊:European Journal of Medicinal Chemistry, 页码:2372-2378 , 文章类型: Article,,卷期:2009年44-6]
- Synthesis and biological evaluation of various aroylpropionic acid derivatives containing 1,3,4-Oxadiazole nucleus is reported here. The compounds (3a-w) were synthesized by cyclizabon of 3-aroylpropionic acids into 1,3,...
- Substituted quinazolines, part 3. Synthesis, in vitro antitumor activity and molecular modeling study of certain 2-thieno-4(3H)-quinazolinone analogs
[作者:Al-Obaid, AM; Abdel-Hamide, SG; El-Kashef, HA; Abdel-Aziz, AAM; El-Azab, AS; Al-Khamees, HA; El-Subbagh, HI,期刊:European Journal of Medicinal Chemistry, 页码:2379-2391 , 文章类型: Article,,卷期:2009年44-6]
- The synthesis of some new 2-thieno-4(3H)-quinazolinone derivatives and their biological evaluation as antitumor agents using the National Cancer Institute (NCI) disease oriented antitumor screen protocol are investigated...
- Synthesis, characterization and cytotoxicity of ammine/ethylamine platinum(II) complexes with carboxylates
[作者:Zhang, JC; Li, YP; Sun, J,期刊:European Journal of Medicinal Chemistry, 页码:2758-2762 , 文章类型: Article,,卷期:2009年44-6]
- Six new mixed ammine/ethylamine platinum(II) complexes with carboxylates [Pt(II)(NH3)(C2H5NH2)X-2] (a-f) (X=CH3COO-, CH2ClCOO-, C6H5-COO-, p-CH3-C6H4-COO-, p-CH3O-C6H4-COO-, p-NO2-C6H4-COO-) (a-f) have been synthesized a...
|