1628796-56-4
1628796-56-4
Chemical Structure
Diethyl succinate-13C4
Synonym(s): 1,4-Diethyl butanedioate-1,2,3,4-13C4
- CAS No.: 1628796-56-4
- Formula:C413C4H14O4
- Molecular Weight:178.16
IUPAC Name: (phenyl-13C6)methanol
InChIKey: DKMROQRQHGEIOW-WKHKRNGSSA-N
SMILES: CCO[13C]([13CH2][13CH2][13C](OCC)=O)=O
Biological Activity: Diethyl succinate-13C4 is the 13C labeled Diethyl succinate[1]. Diethyl succinate (Diethyl Butanedioate) is used at physiological pH and crosses biological membranes, incorporates into cells in tissue culture and is metabolized by the TCA cycle. Diethyl succinate is known to be non-toxic and used in fragrances and flavoring[2].
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Diethyl succinate-13C4 | Diethyl succinate-13C4 is the 13C labeled Diethyl succinate. Diethyl succinate (Diethyl Butanedioate) is used at physiological pH and crosses biological membranes, incorporates into cells in tissue culture and is metabolized by the TCA cycle. Diethyl succinate is known to be non-toxic and used in fragrances and flavoring. | |||||||||||||||||||||
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Diethyl succinate (Standard) | 99.95% | Diethyl succinate (Standard) is the analytical standard of Diethyl succinate. This product is intended for research and analytical applications. Diethyl succinate (Diethyl Butanedioate) can be utilized at physiological pH, allowing it to penetrate biological membranes and integrate into the cells of tissue cultures, where it is metabolized via the tricarboxylic acid cycle. Diethyl succinate modulates the polarization and activation of microglial cells by reducing mitochondrial fission and the levels of reactive oxygen species (ROS), thereby exerting an inflammatory protective effect in primary microglial cells. Furthermore, Diethyl succinate is non-toxic and can be used in flavorings and seasonings. | ||||||||||||||||||||
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Diethyl succinate | 98.0% | Diethyl succinate (Diethyl Butanedioate) can be utilized at physiological pH, allowing it to penetrate biological membranes and integrate into the cells of tissue cultures, where it is metabolized via the tricarboxylic acid cycle. Diethyl succinate modulates the polarization and activation of microglial cells by reducing mitochondrial fission and the levels of reactive oxygen species (ROS), thereby exerting an inflammatory protective effect in primary microglial cells. Furthermore, Diethyl succinate is non-toxic and can be used in flavorings and seasonings. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.96
HY-79076RDiethyl pentanedioate (Standard) -
Similarity Score 0.89
HY-W014126Diethyl heptanedioate -
Similarity Score 0.87
HY-Z9106Lipoic acid impurity 1 -
Similarity Score 0.86
HY-W014799Diethyl 3-oxopentanedioate -
Similarity Score 0.86
HY-W015487Ethyl butyrylacetate -
Similarity Score 0.85
HY-W010293Ethyl 4-oxopentanoate -
Similarity Score 0.84
HY-W081595Ethyl 3-oxoheptanoate -
Similarity Score 0.83
HY-W012597Monoethyl succinate -
Similarity Score 0.82
HY-W015301Dimethyl adipate -
Explore the MedChemAI to find more analogs
References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Zacharias NM, et al. Real-time molecular imaging of tricarboxylic acid cycle metabolism in vivo by hyperpolarized 1-(13)C diethyl succinate. J Am Chem Soc. 2012 Jan 18;134(2):934-43. [Content Brief]
