Results 171 to 180 of about 9,479 (210)
Functionalization of carbon nanospheres with curcumin, polyethylene glycol and folic acid: potential use as drug carriers. [PDF]
De Sales L +2 more
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Molecular basis of SLC19A1-mediated folate and cyclic dinucleotide transport. [PDF]
Zhang Q +12 more
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Carbon-monoxide-driven bioethanol production operates through a tungsten-dependent catalyst. [PDF]
Lemaire ON +3 more
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Degradation of Folic Acid in the Composition of a Conjugate with Polyvinylpyrrolidone and Fullerene C<sub>60</sub> Under UV and E-Beam Irradiation. [PDF]
Borisenkova AA +8 more
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Paper Chromatography of Pterins
Nature, 1949THE detection and identification of pterins in small quantities was carried out by Schopf and Becker1 in the course of their classical work on this class of pigments. They employed a chromatographic technique using 0·004 N aqueous hydrochloric acid or 0·01 N methyl alcoholic hydrochloric acid solutions on micro-absorption columns of alumina or ...
P M, GOOD, A W, JOHNSON
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A Prebiotic Synthesis of Pterins
Chemistry – A European Journal, 2015AbstractThe genesis of life on Earth is a hypothesis of evolutionary science that can be, at least partially, tested experimentally. The prebiotic synthesis of cofactors or coenzymes is a poorly explored issue, likely because their formation under plausible prebiotic conditions is not clear.
Margarita R, Marín-Yaseli +2 more
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Inborn Errors of Pterin Metabolism
Annual Review of Nutrition, 1988HY PERPHENY LALANINEMIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCy 188 GTP Cyclohydrolase I Deficiency 188 6-Pyruvoyl Tetrahydropterin Synthase Deficiency 189 Dihydropteridine Reductase Deficiency 191 Other Forms ...
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Nitric-Oxide-Synthase Inhibitors II — Pterin Antagonists/Anti-Pterins
2000In addition to heme, flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN), nitric oxide synthases (NOS) require tetrahydrobiopterin (H4B). This was first demonstrated for homogenates of stimulated murine macrophages (KWON et al. 1989; TAYEH and MARLETTA 1989). Unlike other enzymes, e.g.
E. R. Werner, H. H. H. W. Schmidt
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Helvetica Chimica Acta, 1948
AbstractDie Herstellung folgender Pterine wird beschrieben: 2‐Äthyl‐thio‐6‐oxypteridin, 2‐Äthylthio‐6‐oxy‐8,9‐diphenylpteridin, 2‐Äthyl‐thio‐6‐oxy‐8,9‐dimethylpteridin, 2‐Äthylthio‐6‐oxy‐8,9‐phenanthreno‐pteridin, 2‐Äthylthio‐6‐oxy‐8,9‐acenaphtenopteridin, 6‐Amino‐iso‐xanthopterin‐carbonsäure, Desimino‐isoxanthopterincarbonsäure.
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AbstractDie Herstellung folgender Pterine wird beschrieben: 2‐Äthyl‐thio‐6‐oxypteridin, 2‐Äthylthio‐6‐oxy‐8,9‐diphenylpteridin, 2‐Äthyl‐thio‐6‐oxy‐8,9‐dimethylpteridin, 2‐Äthylthio‐6‐oxy‐8,9‐phenanthreno‐pteridin, 2‐Äthylthio‐6‐oxy‐8,9‐acenaphtenopteridin, 6‐Amino‐iso‐xanthopterin‐carbonsäure, Desimino‐isoxanthopterincarbonsäure.
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