The research described in the thesis is a continuation of the previous work on the use of benzotriazole in the synthetic chemistry which has been carring out at Department of Medicinal Chemistry, Faculty of Pharmacy and Biochemistry in Zagreb for many years. The thesis includes synthesis of several types of compounds. The initial compound for the synthesis of all the intermediates was benzotriazole carboxylic acid chloride (BtcCl), which upon the reaction with nucleophiles gives reactive products, useful in the preparation of various organic compounds. Amino acid derivatives ureidoamides 4a-o were syntehsized by aminolysis of N-(1- benzotriazolecarbonyl)amino acid chlorides 3 with corresponding aminoalcohols and N- i O- substituted hydroxyureas 6a-l were synthesizes from N-(1-benzotriazolecarbonyl)amino acid amides 5 and hydroxylamines. Nonsteroidal antiinflammatory drugs (NSAID, ibuprofen, fenoprofen and ketoprofen) derivatives were prepared from NSAID hydrazides 11 which were obtained by aminolysis of NSAID benzotriazolides 10 and hydrazine hydrate. The reaction of hydrazides 11 and 1-benzotriazole carboxylic acid amides 7 gave 1-acylsemicarbazides 13a-v, while with 1-(1-benzotriazolecarbonyl)-4-benzyloxysemicarbazide (9) gave 1-acyl-5- benzyloxycarbamoyl-carbazides 14a-c.

Oct 30, 2013  Rheumatoid arthritis, currently regarded as a complex multifactorial disease, was initially characterized as such at the turn of the 19th century. Ever since, multiple lines of investigation have attempted to elucidate the etiological factor(s) involved in disease incidence. Genes – including those risk alleles within HLA-DR4 – have been implicated but are insufficient to explain the vast.

Reactions in melted state in the presence of TEA significantly reduced the reaction time. Dod flips online. 4-Hydroxysemicarbazide compounds 13w-y and 14d-f were prepared by catalytic hydrogenation of O-benzylated compounds 13t-v i 14a-c with Pd/C. Ketoprofen benzotriazolide (10d) reacted with several ureidoamides (4b,i,j,m) and gave esters with two molecules of ketoprofen combined covalently in one („twin drugs“).

The compounds were evaluated for their biological activity in vitro: antitumor, antimicrobial, antiviral and antioxidant activity, inhibition of lipoxygenase and linoleic acid lipid peroxidation. The best antitumor activity was exerted by 6l, antiviral by 13a,g,m, antioxidant by compound 9. The strongest inhibitor of lipoxygenase was 13s.

Tkp 169 2009. Compounds 13c,l,t showed the highest inhibition of linoleic acid lipid peroxidation. It is worth to note that compounds with the highest biological activity contained benzhydryl substituent.

Comment4, Microsoft equation 30 kak polzovatsia, cxeou, Solidworks 2012 torrent,%((, Minisel 1000 kupit, 807, Speed dial 3, 01376, Microchip xc8 compiler,:((.