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1.
Electron. j. biotechnol ; 14(1): 6-7, Jan. 2011. ilus, tab
Article in English | LILACS | ID: lil-591924

ABSTRACT

Plant-antivenom is a computational Websystem about medicinal plants with anti-venom properties. The system consists of a database of these plants, including scientific publications on this subject and amino acid sequences of active principles from venomous animals. The system relates these data allowing their integration through different search applications. For the development of the system, the first surveys were conducted in scientific literature, allowing the creation of a publication database in a library for reading and user interaction. Then, classes of categories were created, allowing the use of tags and the organization of content. This database on medicinal plants has information such as family, species, isolated compounds, activity, inhibited animal venoms, among others. Provision is made for submission of new information by registered users, by the use of wiki tools. Content submitted is released in accordance to permission rules defined by the system. The database on biological venom protein amino acid sequences was structured from the essential information from National Center for Biotechnology Information (NCBI). Plant-antivenom's interface is simple, contributing to a fast and functional access to the system and the integration of different data registered on it. Plant-antivenom system is available on the Internet at http://gbi.fmrp.usp.br/plantantivenom.


Subject(s)
Animals , Antidotes/isolation & purification , Antidotes/chemical synthesis , Antidotes/therapeutic use , Antivenins/administration & dosage , Antivenins/biosynthesis , Antivenins/therapeutic use , Databases, Nucleic Acid , Venoms/adverse effects , Venoms/toxicity , Internet , Plant Extracts
2.
Indian J Physiol Pharmacol ; 2000 Jan; 44(1): 50-6
Article in English | IMSEAR | ID: sea-106293

ABSTRACT

In an attempt to develop effective antidote against organophosphorus intoxication, some new imidazole-pyridinium mono-oximes, long chain pyridinium mono-oximes and cholineacetyltransferase inhibitors were synthesised. These compounds were evaluated for their in vivo therapeutic protection and neuromuscular function studies in rodents. The results indicate that SPK-series oximes may be useful against sarin poisoning without any beneficial effect against VX (O-Ethyl S-2-NN-diisopropylaminoethyl methylphosphonofluoridate) intoxication. The cholineacetyltransferase (ChAT) inhibitors may not be of any help against any of the OP compounds studied in this study.


Subject(s)
Animals , Antidotes/chemical synthesis , Choline O-Acetyltransferase/antagonists & inhibitors , Cholinesterase Inhibitors/toxicity , Enzyme Inhibitors/chemical synthesis , Lethal Dose 50 , Male , Mice , Neuromuscular Junction/drug effects , Organophosphorus Compounds/antagonists & inhibitors , Organothiophosphorus Compounds/toxicity , Oximes/chemical synthesis , Pyridinium Compounds/chemical synthesis , Rats , Rats, Wistar , Sarin/toxicity
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