3-Indolepropionic acid-d2

For research use only. Not for therapeutic Use.

  • CAT Number: S000162
  • CAS Number: 2469257-98-3
  • Molecular Formula: C11H9D2NO2
  • Molecular Weight: 191.22
  • Purity: ≥95%
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3-Indolepropionic Acid-d2 (CAS: 2469257-98-3), a high-quality pharmaceutical research compound designed for advanced studies in neuroprotection and antioxidant research. As a deuterated analog of 3-Indolepropionic acid, it offers enhanced stability and improved pharmacokinetic properties. 3-Indolepropionic Acid-d2 is ideal for use in pharmacological and biochemical research, providing precise and reliable data for your studies. This high-purity compound ensures consistent results, aiding in the development of novel therapies for neurodegenerative diseases and oxidative stress. Trusted by leading laboratories, 3-Indolepropionic Acid-d2 is your go-to solution for cutting-edge neuroprotection research. Unlock new possibilities in brain health and antioxidant therapies with 3-Indolepropionic Acid-d2, where innovation meets reliability.


Catalog Number S000162
CAS Number 2469257-98-3
Molecular Formula C11H9D2NO2
Purity ≥95%
IUPAC Name 2,2-dideuterio-3-(1H-indol-3-yl)propanoic acid
InChI InChI=1S/C11H11NO2/c13-11(14)6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2,(H,13,14)/i6D2
InChIKey GOLXRNDWAUTYKT-NCYHJHSESA-N
SMILES [2H]C([2H])(CC1=CNC2=CC=CC=C21)C(=O)O
Reference

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
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[2]. Wikoff WR, et al. Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites. Proc Natl Acad Sci U S A. 2009 Mar 10;106(10):3698-703.
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[3]. Reiter RJ, et al. Reactive oxygen intermediates, molecular damage, and aging. Relation to melatonin. Ann N Y Acad Sci. 1998 Nov 20;854:410-24.
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[4]. de Mello VDet al. Indolepropionic acid and novel lipid metabolites are associated with a lower risk of type 2 diabetes in the Finnish Diabetes Prevention Study. Sci Rep. 2017 Apr 11;7:46337. doi: 10.1038/srep46337.
[Content Brief]

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