NOUN | SN | SNs | |
SYNO | atomic number 50 | Sn | tin |
NOUN article.ind sg | pl
2 translations
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- олово {с} <Sn> = tin <Sn> [metal]
Show allUsage Examples English
- Thus, the two substrates of this enzyme are CDP-diacylglycerol and sn-glycerol 3-phosphate, whereas its two products are CMP and 3(3-sn-phosphatidyl)-sn-glycerol 1-phosphate.
- Thus, the two substrates of this enzyme are ATP and 1-O-alkyl-sn-glycerol, whereas its two products are ADP and 1-O-alkyl-sn-glycerol 3-phosphate.
- Thus, the two substrates of this enzyme are UDP-galactose and sn-glycerol 3-phosphate, whereas its two products are UDP and 2-(alpha-D-galactosyl)-sn-glycerol 3-phosphate.
- Thus, the two substrates of this enzyme are ADP-glucose and sn-glycerol 3-phosphate, whereas its two products are 2-(beta-D-glucosyl)-sn-glycerol 3-phosphate and ADP.
- Thus, the two substrates of this enzyme are geranylgeranyl diphosphate and "sn"-glyceryl 1-phosphate, whereas its two products are diphosphate and sn-3-O-(geranylgeranyl)glyceryl 1-phosphate.
- Thus, the two substrates of this enzyme are 1-alkyl-2-acetyl-sn-glycero-3-phosphocholine and 1-organyl-2-lyso-sn-glycero-3-phospholipid, whereas its two products are 1-organyl-2-lyso-sn-glycero-3-phosphocholine and 1-alkyl-2-acetyl-sn-glycero-3-phospholipid.
- Thus, the two substrates of this enzyme are 3-sn-phosphatidylcholine and dolichol, whereas its two products are 1-acyl-sn-glycero-3-phosphocholine and acyldolichol.
- Thus, the two substrates of this enzyme are 1-organyl-2-acyl-sn-glycero-3-phosphocholine and 1-organyl-2-lyso-sn-glycero-3-phosphoethanolamine, whereas its two products are 1-organyl-2-acyl-sn-glycero-3-phosphoethanolamine and 1-organyl-2-lyso-sn-glycero-3-phosphocholine.
- The systematic name is 1-("sn"-glycero-3-phospho)-1D-"myo"-inositol glycerophosphohydrolase.
- Thus, the two substrates of this enzyme are 1-(1-alkenyl)-sn-glycero-3-phosphocholine and H2O, whereas its two products are aldehyde and sn-glycero-3-phosphocholine.
- Ether lipid oxidase (alkylglycerol monooxygenase, AGMO) catalyses the conversion of 1-alkyl-sn-glycerol to 1-hydroxyalkyl-sn-glycerol.
- The development of the sn-2 Palmitate structured triglycerides enables the mimicking of both the composition as well as the structure of human milk fat.
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Contains translations by TU Chemnitz and Mr Honey's Business Dictionary (German-English only).
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