IMP

• CAT Number: M071598
• CAS Number: 131-99-7
• Molecular Formula: C10H13N4O8P
• Molecular Weight: 348.21
• Purity: ≥95%
• Target: Endogenous Metabolite
• Storage: -20°C
• IUPAC Name: [(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate
• InChI: InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
• InChIKey: GRSZFWQUAKGDAV-KQYNXXCUSA-N
• SMILES: C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O

IMP (Inosine 5′-monophosphate)（Cat No.:M071598）, is a vital molecule in cellular metabolism and nucleotide biosynthesis. It plays a pivotal role as a precursor in the synthesis of both purine nucleotides and certain coenzymes. IMP is crucial for DNA and RNA synthesis and is involved in energy transfer processes within cells. In the food industry, it is used as a flavor enhancer, particularly in savory products, due to its umami taste. In pharmaceuticals, IMP is researched for its potential therapeutic applications, including its role in immunomodulation.