Indolelactic acid

CAS No. 1821-52-9

Indolelactic acid( —— )

Catalog No. M22552 CAS No. 1821-52-9

Indolelactic acid is a metabolite of tryptophan in Azotobacter vinelandii cultures.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Indolelactic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Indolelactic acid is a metabolite of tryptophan in Azotobacter vinelandii cultures.
  • Description
    Indolelactic acid is a metabolite of tryptophan in Azotobacter vinelandii cultures.
  • In Vitro
    Indolelactic acid (1 mM, 5 days) upregulates CXCR3, granzyme B, and immunoregulatory galectin-1 in Th2 cells.Indolelactic acid (0.1-10mM, 1 h) significantly inhibits LPS-induced inflammation in RAW blue macrophages and Caco-2 cells.Indolelactic acid (0.1-10mM, 1 h) inhibits TNF-α induced inflammation in HT-29 cells.Indolelactic acid (10mM, 1 h) activates the AhR and downstream Nrf2 pathway in Caco-2 cells.Indolelactic acid (5 μM, 24 h) enhances the IFIT2 and RSAD2 mRNA expression in H4 cells stimulated by IL-1β. RT-PCR Cell Line:HT-29 cells Concentration:0.1, 1, 10?mMIncubation Time:1 h Result:Decreased IL-8 level induced by TNF-α, and increased β-defensin 2 and SERT level.
  • In Vivo
    Indolelactic acid (gavage feeding, 10 μM, 5 μL, 5 days, C57BL/6 mice) benefits the immature intestine preferentially. Animal Model:C57BL/6 mice Dosage:10 μM, 5 μL Administration:Gavage feeding, 5 days Result:Upregulated the innate immune response genes in immature mouse intestine (C57-pup-ileum), with no effects on pup-colon or adult intestine.
  • Synonyms
    ——
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1821-52-9
  • Formula Weight
    205.21
  • Molecular Formula
    C11H11NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:82 mg/mL (399.59mM; Need ultrasonic)
  • SMILES
    O=C(O)C(O)Cc2cnc1ccccc12
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Francisco García-Tabares, et al. Production of 3-indoleacetic acid and 3-indolelactic acid in Azotobacter vinelandii cultures supplemented with tryptophan. Appl Microbiol Biotechnol.1987 Mar, 25 (6):502–506.
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