Cas no 347840-19-1 ((±)-Mevalonolactone-4,4,5,5,6,6,6-d7)

(±)-Mevalonolactone-4,4,5,5,6,6,6-d7 is a deuterium-labeled analog of mevalonolactone, a key intermediate in the mevalonate pathway. The incorporation of seven deuterium atoms at the 4, 5, and 6 positions enhances its utility in metabolic and pharmacokinetic studies, providing improved detection sensitivity and reduced metabolic interference in mass spectrometry and NMR analyses. This compound is particularly valuable for tracing biosynthetic pathways, investigating sterol and isoprenoid biosynthesis, and studying enzyme mechanisms. Its high isotopic purity and chemical stability ensure reliable results in isotopic labeling experiments. Suitable for research in biochemistry and pharmacology, it serves as a critical tool for elucidating metabolic flux and enzyme kinetics.
(±)-Mevalonolactone-4,4,5,5,6,6,6-d7 structure
347840-19-1 structure
Product Name:(±)-Mevalonolactone-4,4,5,5,6,6,6-d7
CAS No:347840-19-1
MF:C6H10O3
MW:137.184934139252
CID:302690
PubChem ID:101259392
Update Time:2025-10-30

(±)-Mevalonolactone-4,4,5,5,6,6,6-d7 Chemical and Physical Properties

Names and Identifiers

    • 2H-Pyran-2-one-5,6-d2,tetrahydro-5,6-d2-4-hydroxy-4-(methyl-d3)- (9CI)
    • DL-MEVALONOLACTONE-4,4,5,5,6,6,6-D7
    • MEVALONOLACTONE-4,4,5,5,6,6,6-D7
    • (+/-)-Mevalonolactone-4,4,5,5,6,6,6-d7
    • CS-0374336
    • MS-22805
    • HY-107855S
    • 347840-19-1
    • F93153
    • DL-Mevalonolactone-d7
    • (±)-Mevalonolactone-4,4,5,5,6,6,6-d7
    • Inchi: 1S/C6H10O3/c1-6(8)2-3-9-5(7)4-6/h8H,2-4H2,1H3/i1D3,2D2,3D2
    • InChI Key: JYVXNLLUYHCIIH-NCKGIQLSSA-N
    • SMILES: O1C(CC(C([2H])([2H])[2H])(C([2H])([2H])C1([2H])[2H])O)=O

Computed Properties

  • Exact Mass: 137.107
  • Monoisotopic Mass: 137.107
  • Isotope Atom Count: 7
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 132
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 46.5A^2
  • XLogP3: -0.3

Experimental Properties

  • PSA: 46.53000
  • LogP: 0.07440

(±)-Mevalonolactone-4,4,5,5,6,6,6-d7 Pricemore >>

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Additional information on (±)-Mevalonolactone-4,4,5,5,6,6,6-d7

Compound CAS No. 347840-19-1: (±)-Mevalonolactone-4,4,5,5,6,6,6-d7

The compound CAS No. 347840-19-1, also known as (±)-Mevalonolactone-4,4,5,5,6,6,6-d7, is a highly specialized isotopically labeled derivative of mevalonolactone. This compound has gained significant attention in recent years due to its unique properties and applications in various fields of research. Mevalonolactone itself is a naturally occurring compound that plays a crucial role in the mevalonate pathway, which is essential for the biosynthesis of cholesterol and other isoprenoid compounds. The addition of deuterium atoms at specific positions (positions 4, 5, and 6) in the structure of mevalonolactone creates a stable isotopic tracer that is widely used in metabolic studies and drug development.

Mevalonolactone is a cyclic ester derived from mevalonic acid, which is an intermediate in the biosynthesis of cholesterol. The mevalonate pathway is a critical metabolic pathway in eukaryotic organisms and has been extensively studied for its role in lipid metabolism and cell signaling. The isotopic labeling of mevalonolactone with deuterium atoms at positions 4, 5, and 6 (d7) provides researchers with a powerful tool to track the fate of this compound within biological systems. This labeling allows for precise measurement of metabolic fluxes and enzyme activities using techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.

The synthesis of (±)-Mevalonolactone-4,4,5,5,6,6,6-d7 involves a multi-step process that requires careful control over stereochemistry and isotopic purity. Recent advancements in synthetic chemistry have enabled the production of this compound with high yield and excellent isotopic enrichment. The stereochemical configuration (±) indicates that the compound exists as a racemic mixture of enantiomers. This property makes it suitable for use in both enantioselective studies and applications where stereochemical uniformity is not required.

One of the most significant applications of (±)-Mevalonolactone-4,4,5,5,6,6,d7 is in metabolic research. By incorporating this compound into cellular or animal models, researchers can study the dynamics of lipid metabolism under various physiological or pathological conditions. For example, recent studies have utilized this compound to investigate the effects of statins on cholesterol biosynthesis and to explore novel therapeutic targets for dyslipidemia and related cardiovascular diseases.

In addition to its role as an isotopic tracer in basic research, (±)-Mevalonolactone-4,d7 has also found applications in drug development. The ability to track the fate of this compound within biological systems makes it an invaluable tool for pharmacokinetic studies. Researchers can use this compound to assess drug absorption、distribution、metabolism、and excretion (ADME) properties with high precision.

Recent advances in mass spectrometry techniques have further enhanced the utility of (±)-Mevalonolactone-4,d7 as an analytical tool. High-resolution mass spectrometry (HRMS) allows for precise identification and quantification of this compound even at trace levels within complex biological matrices. This capability has been instrumental in advancing our understanding of lipid metabolism and its regulation under various conditions.

In conclusion, CAS No. 347840-19-1, or (±)-Mevalonolactone-4,d7, represents a valuable tool for researchers studying lipid metabolism、drug development、and metabolic regulation. Its unique properties as an isotopic tracer make it indispensable for advancing our understanding of fundamental biological processes while providing practical applications in clinical research and therapeutic development.

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