Uridine monophosphate structure
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Common Name | Uridine monophosphate | ||
|---|---|---|---|---|
| CAS Number | 58-97-9 | Molecular Weight | 324.181 | |
| Density | 2.2±0.1 g/cm3 | Boiling Point | 700.1±70.0 °C at 760 mmHg | |
| Molecular Formula | C9H13N2O9P | Melting Point | 202 ºC (decomp) | |
| MSDS | USA | Flash Point | 377.2±35.7 °C | |
Use of Uridine monophosphateUridine 5'-monophosphate (5'-Uridylic acid), a monophosphate form of UTP, can be acquired either from a de novo pathway or degradation products of nucleotides and nucleic acids in vivo and is a major nucleotide analogue in mammalian milk[1]. |
| Name | ump |
|---|---|
| Synonym | More Synonyms |
| Description | Uridine 5'-monophosphate (5'-Uridylic acid), a monophosphate form of UTP, can be acquired either from a de novo pathway or degradation products of nucleotides and nucleic acids in vivo and is a major nucleotide analogue in mammalian milk[1]. |
|---|---|
| Related Catalog | |
| Target |
Human Endogenous Metabolite |
| References |
| Density | 2.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 700.1±70.0 °C at 760 mmHg |
| Melting Point | 202 ºC (decomp) |
| Molecular Formula | C9H13N2O9P |
| Molecular Weight | 324.181 |
| Flash Point | 377.2±35.7 °C |
| Exact Mass | 324.035858 |
| PSA | 181.12000 |
| LogP | -1.80 |
| Appearance of Characters | solid |
| Vapour Pressure | 0.0±5.0 mmHg at 25°C |
| Index of Refraction | 1.754 |
| Storage condition | −20°C |
| Water Solubility | H2O: soluble50mg/mL, clear, colorless |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Characterization, antioxidative and ACE inhibitory properties of hydrolysates obtained from thornback ray (Raja clavata) muscle.
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Clay catalyzed RNA synthesis under Martian conditions: Application for Mars return samples.
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Pyrimidine homeostasis is accomplished by directed overflow metabolism.
Nature 500(7461) , 237-41, (2013) Cellular metabolism converts available nutrients into usable energy and biomass precursors. The process is regulated to facilitate efficient nutrient use and metabolic homeostasis. Feedback inhibition... |
| 5'-Uridylic acid |
| Uridine monophosphate |
| uridinemonophosphate |
| 4-Hydroxy-1-(5-O-phosphono-β-D-ribofuranosyl)-2(1H)-pyrimidinone |
| U 5'-P |
| UMP |
| Uridylate |
| 2(1H)-Pyrimidinone, 4-hydroxy-1-(5-O-phosphono-β-D-ribofuranosyl)- |
| Uridine 5'-monophosphate |
| uridine-5′-monophosphate |
| uridine 5′-monophosphate |
| uridinephosphate |
| Diquafosol Impurity 1 |
| EINECS 200-408-0 |