3128-06-1
Chemical Structure
Glurate
Synonym(s): 4-Acetylbutyric acid; 5-Oxohexanoic acid; NSC-5281
- CAS No.: 3128-06-1
- Formula:C6H10O3
- Molecular Weight:130.14
IUPAC Name: 5-oxohexanoic acid
InChIKey: MGTZCLMLSSAXLD-UHFFFAOYSA-N
SMILES: CC(=O)CCCC(=O)O
Biological Activity: Glurate (4-Acetylbutyric acid) is an acylating agent. Glurate can be used in the development of antiviral compounds, especially those targeting retroviruses such as herpes virus and HIV. Glurate can be used in the synthesis of acyclic nucleoside derivatives and 5-hydroxyhexanoic acid[1][2].
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Glurate | 98.54% | Glurate (4-Acetylbutyric acid) is an acylating agent. Glurate can be used in the development of antiviral compounds, especially those targeting retroviruses such as herpes virus and HIV. Glurate can be used in the synthesis of acyclic nucleoside derivatives and 5-hydroxyhexanoic acid. | ||||||||||||||||||||
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Glurate (Standard) | ≥98% | Glurate (Standard) is the analytical standard of Glurate (HY-W001957). This product is used for research and analytical applications. Glurate (4-Acetylbutyric acid) is an acylating agent. Glurate can be used in the development of antiviral compounds, especially those targeting retroviruses such as herpes virus and HIV. Glurate can be used in the synthesis of acyclic nucleoside derivatives and 5-hydroxyhexanoic acid. | ||||||||||||||||||||
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Glurate-d5 | Glurate-d5 (4-Acetylbutyric acid-d5; 5-Oxohexanoic acid-d5; NSC-5281-d5) is the deuterium labeled Glurate (HY-W001957). Glurate (4-Acetylbutyric acid) is an acylating agent. Glurate can be used in the development of antiviral compounds, especially those targeting retroviruses such as herpes virus and HIV. Glurate can be used in the synthesis of acyclic nucleoside derivatives and 5-hydroxyhexanoic acid. | |||||||||||||||||||||
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- [1]. Per Engelhardt, et al. Synthesis of acyclic nucleosides. Patent WO1997030052A1.
- [2]. Valentin H E, et al. Identification of 5-hydroxyhexanoic acid, 4-hydroxyheptanoic acid and 4-hydroxyoctanoic acid as new constituents of bacterial polyhydroxyalkanoic acids. Applied microbiology and biotechnology, 1996, 46: 261-267.
Keywords