1935
DOI: 10.1039/jr9350000855
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Cited by 7 publications
(3 citation statements)
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“…Recent work with radioactive phosphorus and with deuterium as indicators has shown a very active turnover of the phospholipids of the kidney in the course of normal metabolism, indeed almost as rapid a metabolism as that within the liver itself (21)(22)(23)(24)(25)(26). The findings in our experiments may not at present be open to any simple explanation, but it seems quite possible that future work may prove that they are in some way connected with the r61e of the kidney in normal phospholipid metabolism.…”
Section: Discussionmentioning
confidence: 99%
“…Recent work with radioactive phosphorus and with deuterium as indicators has shown a very active turnover of the phospholipids of the kidney in the course of normal metabolism, indeed almost as rapid a metabolism as that within the liver itself (21)(22)(23)(24)(25)(26). The findings in our experiments may not at present be open to any simple explanation, but it seems quite possible that future work may prove that they are in some way connected with the r61e of the kidney in normal phospholipid metabolism.…”
Section: Discussionmentioning
confidence: 99%
“…Recent work with radioactive phosphorus and with deuterium as indicators has shown a very active turnover of the phospholipids of the kidney in the course of normal metabolism, indeed almost as rapid a metabolism as that within the liver itself (21)(22)(23)(24)(25)(26). The findings in our experiments may not at present be open to any simple explanation, but it seems quite possible that future work may prove that they are in some way connected with the r61e of the kidney in normal phospholipid metabolism.…”
Section: Discussionmentioning
confidence: 99%
“…S-Phenylthiobenzoate[24] was eluted from column chromatography using n-hexane-ether (2:1, v/v), mp and mmp 56-60 8C. Diphenyl acetylene[25] was eluted from column chromatography using successive portions of n-hexaneether (2:1, v/v), mp and mmp 63-65 8C; picrate derivative (ethanol), mp 110-112 8C; m/e 196. 2,3,4,5-Tetraphenylfuran[26] was eluted using n-hexane-CHCl 3 (17:3, v/v) mixtures, mp and mmp 175 8C; m/e 372.…”
mentioning
confidence: 99%