| pubmed-article:5271178 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:5271178 | lifeskim:mentions | umls-concept:C0035323 | lld:lifeskim |
| pubmed-article:5271178 | lifeskim:mentions | umls-concept:C0035499 | lld:lifeskim |
| pubmed-article:5271178 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
| pubmed-article:5271178 | lifeskim:mentions | umls-concept:C0064073 | lld:lifeskim |
| pubmed-article:5271178 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:5271178 | pubmed:dateCreated | 1970-10-6 | lld:pubmed |
| pubmed-article:5271178 | pubmed:abstractText | The preparation and properties of three geometric isomers of 13-desmethyl retinal (13-dmr) are described. They are analogous to the all-trans, 11-cis, and 9-cis isomers of retinal since two of the cis isomers combine with cattle opsin to form pigments which are spectrally indistinguishable from rhodopsin and isorhodopsin and the all-trans isomer is unreactive.The pigment which resembles rhodopsin, 13-desmethyl (13-dm) rhodopsin, is formed at about one ninth the rate at which 11-cis retinal reacts with opsin at 20 degrees C. The reaction with 13-dmr does not go to completion; and 0.05 M hydroxylamine, to which rhodopsin is stable, decomposes 13-dm rhodopsin. Irradiation of 13-dm rhodopsin results in a cis --> trans isomerization of the chromophore; but the photosensitivity of 13-dm rhodopsin is only 40 per cent that of rhodopsin.13-dm isorhodopsin, the 13-desmethyl analogue of isorhodopsin, is formed at approximately the same specific rate as 13-dm rhodopsin. The reaction goes to completion and the pigment is not decomposed by 0.03 M hydroxylamine. 13-dm isorhodopsin can also be photolyzed to the all-trans chromophore plus opsin. | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:language | eng | lld:pubmed |
| pubmed-article:5271178 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:5271178 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:5271178 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:5271178 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:5271178 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:5271178 | pubmed:author | pubmed-author:NelsonRR | lld:pubmed |
| pubmed-article:5271178 | pubmed:author | pubmed-author:KropfAA | lld:pubmed |
| pubmed-article:5271178 | pubmed:author | pubmed-author:deRielJ KJK | lld:pubmed |
| pubmed-article:5271178 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:5271178 | pubmed:volume | 66 | lld:pubmed |
| pubmed-article:5271178 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:5271178 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:5271178 | pubmed:pagination | 531-8 | lld:pubmed |
| pubmed-article:5271178 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:meshHeading | pubmed-meshheading:5271178-... | lld:pubmed |
| pubmed-article:5271178 | pubmed:year | 1970 | lld:pubmed |
| pubmed-article:5271178 | pubmed:articleTitle | 13-desmethyl rhodopsin and 13-desmethyl isorhodopsin: visual pigment analogues. | lld:pubmed |
| pubmed-article:5271178 | pubmed:publicationType | Journal Article | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:5271178 | lld:pubmed |
