thiourea has been researched along with Poisoning* in 5 studies
5 other study(ies) available for thiourea and Poisoning
| Article | Year |
|---|---|
Distribution and behavior of isoselenouronium salts in the body. V. Acute toxicity and metabolic fate of selenium derivatives.
The acute toxicity of AESe, 2-ASe, and Se-MEG was estimated in mice after i.v., i.p. and s.c. application. In all forms of application, 2-ASe was found to have the lowest toxicity. The study of excretion showed that administered compounds are excreted practically completely within seven days, mostly by urine. The excretion by faeces is very low and by exhalation is under the threshold of demonstrability. The metabolism of 2-ASe is slow, most of it is excreted without any change; AESe is transformed into a mixture of 2-ASe and Se-MEG. Se-MEG is excreted by urine totally metabolized as trimethylselenium ion. Topics: Acute Disease; Animals; Azoles; Feces; Isomerism; Isothiuronium; Kinetics; Lethal Dose 50; Male; Mice; Poisoning; Radiation-Protective Agents; Selenium; Thiourea | 1976 |
[Pharmacologic-endocrinological findings in animal experiments with TURISYNCHRON and SUISYNCHROM. 2. Toxicologic findings].
Acute, subacute and chronic toxicity of TURISYNCHRON and its zinc complex (SUISYNCHRON) was tested in mice, rats and dogs. The acute toxicity of SUISYNCHRON was lower than that of TURISYNCHRON in mice and rats. Ulcerative lesions in the duodenum produced by high doses of SUISYNCHRON were quantitatively less pronounced than those produced by similar doses of TURISYNCHRON. Subacute toxicity testing in rats showed that neither preparation had any toxic effect on haematological, clinical chemical or histological criteria in the dosages selected. Chronic toxicity testing of TURISYNCHRON in dogs did not reveal any evidence of toxic damage. Topics: Acute Disease; Administration, Oral; Animals; Atropine; Body Weight; Chlorpromazine; Chronic Disease; Duodenal Diseases; Female; Injections, Subcutaneous; Lethal Dose 50; Maternal-Fetal Exchange; Methallibure; Mice; Organ Size; Papaverine; Peptic Ulcer; Poisoning; Pregnancy; Rats; Sex Factors; Structure-Activity Relationship; Thiourea; Zinc | 1974 |
[HEMATOPOIETIC AND BLOOD CHANGES IN CHRONIC THIOUREA POISONING].
Topics: Bone Marrow Diseases; Chemical Industry; Hematologic Diseases; Humans; Lymph Nodes; Occupational Diseases; Poisoning; Spleen; Thiourea; Toxicology | 1964 |
Toxic hazards. Rat poisons. III. Thallium, strychnine & ANTU.
Topics: Animals; Heavy Metal Poisoning; Metals, Heavy; Naphthalenes; Poisoning; Poisons; Rats; Strychnine; Thallium; Thiourea | 1958 |
Alpha-Naphthylthiourea (ANTU) as a cause of poisoning in dogs and its chemical identification in material of animal origin.
Topics: Animals; Anti-Bacterial Agents; Dogs; Humans; Hydrocarbons, Aromatic; Naphthalenes; Poisoning; Thiourea | 1953 |