uridine 5-monophosphate free acid
uridine 5-monophosphate free acid
CAS: 58-97-9
Molecular Formula: C9H13N2O9P
uridine 5-monophosphate free acid - Names and Identifiers
| Name | uridine 5-monophosphate free acid |
| Synonyms | UMP Uridylic Acid 5'-uridylic acid Uridine 5'-monophosphate Uridine-5''-monophosphoric acid uridine 5-(dihydrogen phosphate) uridine 5-monophosphate free acid |
| CAS | 58-97-9 |
| EINECS | 200-408-0 |
| InChI | InChI=1/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1 |
uridine 5-monophosphate free acid - Physico-chemical Properties
| Molecular Formula | C9H13N2O9P |
| Molar Mass | 324.18 |
| Density | 1.865g/cm3 |
| Storage Condition | -20℃ |
| Sensitive | Easily absorbing moisture |
| Refractive Index | 1.643 |
| MDL | MFCD00067346 |
| Use | Used as nucleic acid drug intermediates, health food and biochemical reagents, and used in the manufacture of uridine triphosphate, polyglandular urine, fluoride and other drugs |
uridine 5-monophosphate free acid - Upstream Downstream Industry
| Raw Materials | Ribonucleic Acid, Transfer |
uridine 5-monophosphate free acid - Reference
| Reference Show more | 1. [IF=3.638] Meina Zhang et al."Effects of fermentation with Lactobacillus fermentum 21828 on the nutritional characteristics and antioxidant activity of Lentinus edodes liquid."Journal Of The Science Of Food And Agriculture. 2021 Dec 14 |
uridine 5-monophosphate free acid - Introduction
uridine 5-monophosphate free acid, the chemical name is dehydrogenated uridine 5-monophosphate free acid(uridine 5-monophosphate free acid), is a purine nucleotide. It is the acidic form of uridine, composed of uracil and glucose, and has more physiological functions.
uridine 5-monophosphate free acid widely exists in organisms. It is an important part of RNA and DNA and participates in the biosynthesis and metabolism of nucleic acid. In addition, it is also involved in a variety of biochemical reactions, such as energy metabolism, signal transduction and cell differentiation.
there are two main ways to make uridine 5-monophosphate free acid. One is through chemical synthesis, which is synthesized by reacting deoxyuridine with anhydrous phosphoric acid; the other is through biosynthesis, which is synthesized by stepwise conversion using appropriate substrates and enzymes in the cell.
uridine 5-monophosphate free acid is generally considered to be a relatively safe compound. However, it is important to follow proper operating procedures and safety measures if required. Wear appropriate personal protective equipment, such as lab gloves and goggles, when preparing and handling uridine 5-monophosphate free acid. And avoid direct contact with skin, eyes and mucous membranes. If it accidentally enters the eyes or skin, rinse immediately with plenty of water and consult a doctor. In addition, uridine 5-monophosphate free acid should be stored in a dry and cool place to avoid contact with oxygen to avoid degradation and decomposition. During use or handling, care should be taken to avoid the production of dust and gas to avoid accidental injury caused by inhalation or oral administration. Please take care to dispose of chemical waste properly and in accordance with local regulations.
uridine 5-monophosphate free acid widely exists in organisms. It is an important part of RNA and DNA and participates in the biosynthesis and metabolism of nucleic acid. In addition, it is also involved in a variety of biochemical reactions, such as energy metabolism, signal transduction and cell differentiation.
there are two main ways to make uridine 5-monophosphate free acid. One is through chemical synthesis, which is synthesized by reacting deoxyuridine with anhydrous phosphoric acid; the other is through biosynthesis, which is synthesized by stepwise conversion using appropriate substrates and enzymes in the cell.
uridine 5-monophosphate free acid is generally considered to be a relatively safe compound. However, it is important to follow proper operating procedures and safety measures if required. Wear appropriate personal protective equipment, such as lab gloves and goggles, when preparing and handling uridine 5-monophosphate free acid. And avoid direct contact with skin, eyes and mucous membranes. If it accidentally enters the eyes or skin, rinse immediately with plenty of water and consult a doctor. In addition, uridine 5-monophosphate free acid should be stored in a dry and cool place to avoid contact with oxygen to avoid degradation and decomposition. During use or handling, care should be taken to avoid the production of dust and gas to avoid accidental injury caused by inhalation or oral administration. Please take care to dispose of chemical waste properly and in accordance with local regulations.
Last Update：2024-04-09 20:52:54
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