Date published: 2026-1-31

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(±)-Phenylsuccinic acid (CAS 635-51-8)

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Alternate Names:
Phenylsuccinic acid
CAS Number:
635-51-8
Molecular Weight:
194.18
Molecular Formula:
C10H10O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(±)-Phenylsuccinic acid, a dicarboxylic acid derived from benzene, possesses two carboxylic acid groups. It has garnered attention as an inhibitor of the enzyme dihydroorotate dehydrogenase (DHODH), in pyrimidine nucleotide metabolism. Notably, (±)-Phenylsuccinic acid has exhibited inhibitory effects on cancer cell growth in vitro. In the realm of inflammation research, its potential in modulating the activity of nuclear factor kappa B (NF-κB), a key transcription factor in the inflammatory response, has been explored. Research findings indicate that (±)-Phenylsuccinic acid effectively hinders NF-κB activity.


(±)-Phenylsuccinic acid (CAS 635-51-8) References

  1. Surface-enhanced Raman scattering and the adsorption behavior of (RS)-phenylsuccinic acid.  |  Sajan, D., et al. 2006. Spectrochim Acta A Mol Biomol Spectrosc. 64: 580-5. PMID: 16458060
  2. The Fate in the Animal Body of Phenylsuccinic Acid and beta-Phenylhexoic Acid.  |  Clutterbuck, PW. and Raper, HS. 1925. Biochem J. 19: 911-4. PMID: 16743612
  3. Enantioseparation of phenylsuccinic acid by high speed counter-current chromatography using hydroxypropyl-β-cyclodextrin as chiral selector.  |  Tong, S., et al. 2011. J Chromatogr A. 1218: 5602-8. PMID: 21752382
  4. Separation of phenylsuccinic acid enantiomers using biphasic chiral recognition high-speed countercurrent chromatography.  |  Sun, G., et al. 2014. J Sep Sci. 37: 1736-41. PMID: 24788958
  5. Enantioselective extraction of phenylsuccinic acid in aqueous two-phase systems based on acetone and β-cyclodextrin derivative: Modeling and optimization through response surface methodology.  |  Wang, J., et al. 2016. J Chromatogr A. 1467: 490-496. PMID: 27372416
  6. Chiral Separations by Countercurrent Chromatography.  |  Tong, SQ. 2019. Methods Mol Biol. 1985: 321-337. PMID: 31069742
  7. Stable Chitosan-Based Nanoparticles Using Polyphosphoric Acid or Hexametaphosphate for Tandem Ionotropic/Covalent Crosslinking and Subsequent Investigation as Novel Vehicles for Drug Delivery.  |  Saeed, RM., et al. 2020. Front Bioeng Biotechnol. 8: 4. PMID: 32039190
  8. Hydroxypropyl-β-cyclodextrin encapsulated stationary phase based on silica monolith particles for enantioseparation in liquid chromatography.  |  Lu, Y. and Sun, G. 2021. J Sep Sci. 44: 735-743. PMID: 33253443
  9. Efficient carboxylation of styrene and carbon dioxide by single-atomic copper electrocatalyst.  |  Quan, Y., et al. 2021. J Colloid Interface Sci. 601: 378-384. PMID: 34087598
  10. Synthesis and properties of cyclic derivatives of phenylsuccinic acid. IX. New phenylsuccinimide derivatives with anticonvulsant properties.  |  Lange, J., et al. 1987. Acta Pol Pharm. 44: 249-54. PMID: 3447414
  11. Lipase-based MIL-100(Fe) biocomposites as chiral stationary phase for high-efficiency capillary electrochromatographic enantioseparation.  |  Sun, G., et al. 2023. Mikrochim Acta. 190: 84. PMID: 36749401
  12. Soft drugs. 13: Design and evaluation of phenylsuccinic analogs of scopolamine as soft anticholinergics.  |  Kumar, GN., et al. 1993. Drug Des Discov. 10: 1-9. PMID: 8399990
  13. Synthesis of N-alkyloamino- or arylo-imide derivatives of succinic acid.  |  Lucka-Sobstel, B., et al. 1977. Arch Immunol Ther Exp (Warsz). 25: 285-9. PMID: 869683

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(±)-Phenylsuccinic acid, 100 g

sc-250708
100 g
$79.00