5′-UMP-Na2 - ≥99% , CAS No.3387-36-8

CAS: 3387-36-8 Cat. No.: U106892 Fórmula: C₉H₁₁N₂Na₂O₉P Peso molecular: 368.15 Beilstein Registry Number: 3582885 Número CE: 222-211-9 PubChem CID: 169020

GRADE & PURITY ≥99%

Synonyms

5'-UMP | SCHEMBL842020 | U0021 | UMP sodium salt | Uridine 5'-monophosphate disodium | DisodiumUridine-5-Monophosphate | Uridine 5'MP, disodium salt | Uridine 5'-monophosphate, disodium salt | DISODIUM URIDINE MONOPHOSPHATE [WHO-DD] | 5'-Uridylic Acid Dis

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

5'-UMP | SCHEMBL842020 | U0021 | UMP sodium salt | Uridine 5'-monophosphate disodium | DisodiumUridine-5-Monophosphate | Uridine 5'MP, disodium salt | Uridine 5'-monophosphate, disodium salt | DISODIUM URIDINE MONOPHOSPHATE [WHO-DD] | 5'-Uridylic Acid Dis

Especificações e pureza

≥99%

Mecanismos bioquímicos e fisiológicos

Nucleotide that is a major component of ribonucleic acid. It is found in dietary supplements as well as natural RNA rich foods and has been shown to increase cognitive function in animals.

Condições de armazenamento de armazenamento

Store at -20°C

Enviado em

Ice chest + Ice pads

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥99%

Nomes e identificadores

• Pubchem Sid: 504757627
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757627
• Sorrisos canónicos: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
• IUPAC Name: disodium;[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
• InChIKey: KURVIXMFFSNONZ-WFIJOQBCSA-L
• INCHI: 1S/C9H13N2O9P.2Na/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);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1
• SMILES isoméricas: C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
• WGK Alemanha: 2
• RTECS: YU7975000
• PubChem CID: 169020
• Peso molecular: 368.15
• Beilstein: 3582885
• Reaxy-Rn: 3582885

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Classe Pyrimidine nucleotides
      • Subclass Pyrimidine ribonucleotides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Classe: Pyrimidine nucleotides
• Subclass: Pyrimidine ribonucleotides
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine ribonucleoside monophosphates
• Alternative Parents: Pentose phosphates Glycosylamines Monosaccharide phosphates Pyrimidones Hydropyrimidines Alkyl phosphates Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Ureas Secondary alcohols Lactams 1,2-diols Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidine ribonucleoside monophosphate - Pentose-5-phosphate - Pentose phosphate - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Pyrimidone - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - Monosaccharide - Hydropyrimidine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Urea - Secondary alcohol - Lactam - 1,2-diol - Oxacycle - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside monophosphates. These are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriedades químicas e físicas

• Sensibilidade: Heat Sensitive
• Rotação específica [α]: -14 ° (C=1, H2O)
• Ponto de fusão (°C): 208-210°C
• Peso molecular: 368.140 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 3
• Exact Mass: 368 Da
• Monoisotopic Mass: 368 Da
• Topological Polar Surface Area: 172.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 506.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

Referências

1. Chujing Yang, Zhiwei Zhang, Jingqi Chen, Xinying Zhang, Yankai Dai, Xuyi Li, Yingying Chen, Jiaqiang Xu, Lingyan Feng.  (2023)  Multiple switchable circularly polarized luminescence from nucleotide/terbium(III) complexes.  NEW JOURNAL OF CHEMISTRY,  47  (9): (4472-4477).  [PMID:] [10.1039/D2NJ06145G]

2. Quan Li, Zhile Bai, Xingjun Xi, Zhiwei Guo, Cong Liu, Xuerui Liu, Xiaoyan Zhao, Zhiyue Li, Yong Cheng, Yun Wei.  (2020)  Rapid microwave-assisted green synthesis of guanine-derived carbon dots for highly selective detection of Ag+ in aqueous solution.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:33257251] [10.1016/j.saa.2020.119208]

3. Zhihong Guan, Ruobo Chen, Kaixin Liu, Li Fu, Ling Li, Li Jia.  (2024)  Copper ion as a peroxidase mimic for fluorescent detection of casein phosphopeptide by a 3D-printed portable device.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112501]

4. Xuetao Yan, Lifei Chen, Yuze Ren, Kaixuan Cui, Tianliang Li, Lixing Lin, Zeyu Li, Yingying Chen, Zhenzhen Li, Lingyan Feng.  (2026)  Nucleotide-Based White Circularly Polarized Luminescence Materials in Lanthanide Deep Eutectic Solvents.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.5c08455]

5. Liying Cui, Yong Wang, Qin Zhang, Xin Liu.  (2026)  Closed-loop recyclable and robust underwater adhesive featuring real-time detectable adhesion interface.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.175232]