| pubmed-article:177750 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0001407 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0003286 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0028027 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0031436 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0030011 | lld:lifeskim |
| pubmed-article:177750 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
| pubmed-article:177750 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:177750 | pubmed:dateCreated | 1976-7-6 | lld:pubmed |
| pubmed-article:177750 | pubmed:abstractText | Several Several 10-(1-acetyl-4-arylthiosemicarbazido) phenothiazines and their corresponding cyclized 10-(2-arylimino-3-acetylamino-4-thiazolidonyl)phenothiazines were synthetized and characterized by their sharp melting points and elemental analyses. All compounds inhibited nicotinamide adenine dinucleotide (NAD)-dependent oxidation of pyruvate and alpha-ketoglutarate selectively, whereas NAD-independent oxidation of succinate remained unaltered. All phenothiazine derivatives exhibited anticonvulsant activity, which was reflected by the 20-60% protection observed against pentylenetetrazol-induced convulsions in mice. The ability of substituted thiosemicarbazidophenothiazines to inhibit cellular respiratory activity was reduced considerably by cyclization to the corresponding substituted thiazolidinophenothiazines. On the other hand, cyclization generally resulted in increased anticonvulsant activity. Thus, the anticonvulsant activity possessed by these substituted phenothiazines bore no relationship with their ability to inhibit selectively the NAD-dependent oxidations. Selective inhibition of NAD-dependent oxidation of pyruvate and alpha-ketoglutarate in isolated rat brain mitochondria by some 10-(1-acetyl-4-arylthiosemicarbazido) phenothiazines was concentration dependent and competitive in nature. | lld:pubmed |
| pubmed-article:177750 | pubmed:language | eng | lld:pubmed |
| pubmed-article:177750 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:177750 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:177750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:177750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:177750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:177750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:177750 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:177750 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:177750 | pubmed:issn | 0022-3549 | lld:pubmed |
| pubmed-article:177750 | pubmed:author | pubmed-author:SinghS PSP | lld:pubmed |
| pubmed-article:177750 | pubmed:author | pubmed-author:ParmarS SSS | lld:pubmed |
| pubmed-article:177750 | pubmed:author | pubmed-author:AliBB | lld:pubmed |
| pubmed-article:177750 | pubmed:author | pubmed-author:De BoerBB | lld:pubmed |
| pubmed-article:177750 | pubmed:author | pubmed-author:AuyongT KTK | lld:pubmed |
| pubmed-article:177750 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:177750 | pubmed:volume | 65 | lld:pubmed |
| pubmed-article:177750 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:177750 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:177750 | pubmed:pagination | 391-6 | lld:pubmed |
| pubmed-article:177750 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-A... | lld:pubmed |
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| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-O... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-F... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-M... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-A... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-N... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-M... | lld:pubmed |
| pubmed-article:177750 | pubmed:meshHeading | pubmed-meshheading:177750-D... | lld:pubmed |
| pubmed-article:177750 | pubmed:year | 1976 | lld:pubmed |
| pubmed-article:177750 | pubmed:articleTitle | Anticonvulsant activity and selective inhibition of nicotinamide adenine dinucleotide-dependent oxidations by 10-(2-arylimino-3-acetylamino-4-thiazolidonyl) phenothiazines. | lld:pubmed |
| pubmed-article:177750 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:177750 | pubmed:publicationType | In Vitro | lld:pubmed |
| pubmed-article:177750 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:177750 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
