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Orotic acid monohydrate
🥰Excellent
Catalog No. T5078Cas No. 50887-69-9
Alias Orotic Acid Monohydrate, 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid hydrate, 2,4-dioxo-1H-pyrimidine-6-carboxylic acid hydrate
Orotic acid monohydrate is an intermediate product in pyrimidine metabolism.
Orotic acid monohydrate
🥰Excellent
Purity: 100%
Catalog No. T5078Alias Orotic Acid Monohydrate, 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid hydrate, 2,4-dioxo-1H-pyrimidine-6-carboxylic acid hydrateCas No. 50887-69-9
Orotic acid monohydrate is an intermediate product in pyrimidine metabolism.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 g | $29 | In Stock |
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Purity:100%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Orotic acid monohydrate is an intermediate product in pyrimidine metabolism. |
| In vitro | Orotic acid increases cell proliferation and decreases apoptosis in serum-starved SK-Hep1 hepatocellular carcinoma cells, which may ascribe to the inhibition of AMP-activated protein kinase (AMPK) phosphorylation and thus activation of mammalian target of rapamycin complex 1 (mTORC1) [1]. |
| In vivo | Male Fischer 344 rats (130-150 g) to two-thirds PH in the absence or in the presence of Orotic acid (a 300-mg tablet of Orotic acid methyl ester implanted intraperitoneally at the time of two-thirds PH). treatment with Orotic acid resulted in a near-100% inhibition of RNR induced by two-thirds PH in rat liver, as monitored by enzyme activity and protein level [2]. Feeding 1% Orotic acid with diet decreased the phosphorylation of AMPK and increased the maturation of SREBP-1 and the expression of SREBP-responsive genes in the rat liver. Orotic acid-induced lipid accumulation was also completely inhibited by rapamycin. Mouse hepatocytes and mice were resistant to Orotic acid-induced lipogenesis because of little if any response in AMPK and downstream effectors [3]. |
| Alias | Orotic Acid Monohydrate, 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid hydrate, 2,4-dioxo-1H-pyrimidine-6-carboxylic acid hydrate |
| Molecular Weight | 174.11 |
| Formula | C5H6N2O5 |
| Cas No. | 50887-69-9 |
| Smiles | O.OC(=O)C1=CC(=O)NC(=O)N1 |
| Relative Density. | 1.642 g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||
| Solubility Information | DMSO: 2.5 mg/mL (14.36 mM), Sonication is recommended.  Ethanol: < 1 mg/mL (insoluble or slightly soluble) H2O: < 1 mg/mL (insoluble or slightly soluble) | ||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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