O2875

Orotic acid potassium salt

≥98%

• Synonyme(s) : 6-Carboxy-2,4-dihydroxypyrimidine, Uracil-6-carboxylic acid
• Formule linéaire : C₅H₃N₂O₄K
• Numéro CAS: 24598-73-0
• Poids moléculaire : 194.19
• NACRES: NA.51
• PubChem Substance ID: 24897970
• UNSPSC Code: 41106305
• EC Number: 246-341-0
• MDL number: MFCD00039118
• Assay: ≥98%
• Form: powder
• Solubility: 1 M NaOH: 25 mg/mL, clear to slightly hazy, colorless to faintly yellow

Propriétés

• Quality Segment: 200
• assay: ≥98%
• form: powder
• solubility: 1 M NaOH: 25 mg/mL, clear to slightly hazy, colorless to faintly yellow
• SMILES string: [K+].[O-]C(=O)C1=CC(=O)NC(=O)N1
• InChI: 1S/C5H4N2O4.K/c8-3-1-2(4(9)10)6-5(11)7-3;/h1H,(H,9,10)(H2,6,7,8,11);/q;+1/p-1
• InChI key: DHBUISJCVRMTAZ-UHFFFAOYSA-M

Description

Application

Orotic acid (OA) is an intermediate in de novo pyrimidine biosynthesis that may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from 5′-phospho-α-d-ribose 1′-diphosphate (PRPP) to orotic acid (OA), forming pyrophosphate and orotidine 5′-monophosphate (OMP). Orotic acid is used as a starting material for the potential commercial bioproduction of uridine 5′-monophosphate (UMP) by microbes such as Corynebacterium ammoniagenes (ATCC 6872) or Saccharomyces cerevisiae. OA may be used to study the AMPK/SREBP-1 dependent cell signaling pathway and transcription regulation mechanisms that induce hepatic lipogenesis.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)