Reference

Development of tolerance to the antinociceptive effect but not to the toxicity of trimethyltin after repeated exposure

Development of tolerance to the antinociceptive effect but not to the toxicity of trimethyltin after repeated exposure. Doctor, Shreenath V.; Costa, Lucio G.; Murphy, Sheldon D. (Toxicol. Branch, Chem. Res. Dev. Cent., Aberdeen Proving Ground, MD 21010, USA). Dev. Toxicol. Environ. Sci., 11(Dev. Sci. Pract. Toxicol.), 587-90 (English) 1983. CODEN: DTESD7. ISSN: 0165-2214. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Section cross-reference(s): 1 Trimethyltin (TMT) [1631-73-8] (2.13 mg/kg/wk for 4 wk, i.p.)-pretreated mice were tolerant to the antinociceptive effect of an acute dose of TMT (4.26 mg/kg, i.p.). TMT-pretreated mice were cross-tolerant to the antinociceptive effect of morphine (I) [57-27-2] (5 mg/kg, i.p.) and GABA uptake inhibitor Et nipecotate [5006-62-2] (35 mg/kg, i.p.) but not to the muscarinic agonist oxotremorine [70-22-4] (0.1 mg/kg, i.p.). TMT pretreatment did not significantly protect animals from the hypothermic effect of TMT, nor were TMT-pretreated animals tolerant to the acute lethal toxicity of TMT.

Synthesis of tricyclic skeletons mediated by (diene)Fe(CO)3 complexes

Synthesis of tricyclic skeletons mediated by (diene)Fe(CO)3 complexes. Yeh, Ming-Chang P.; Chuang, Li-Wen (Department of Chemistry, National Taiwan Normal University, Taipei 117, Taiwan). Journal of the Chinese Chemical Society (Taipei), 44(3), 291-297 (English) 1997 Chinese Chemical Society. CODEN: JCCTAC. ISSN: 0009-4536. DOCUMENT TYPE: Journal CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) Section cross-reference(s): 24, 29 Sequential addns. of carbon nucleophiles to the (h5-pentadienyl)Fe(CO)3 cation afforded tricyclo[6.3.0.In this article, certain chemicals are used. One of their cas registry numbers is 5006-62-2 02,6]undecane, tricyclo[6.4.0.02,6]dodecane, tricyclo[7.3.0.02,7]dodecane and tricyclo[7.In this article, certain chemicals are used. One of their cas registry numbers is 5006-62-2 4.0.02,7]tridecane derivs. The same strategy can also be applied to construct heterotricyclic skeletons. ..