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N-3-Oxo-octanoyl-L-homoserine lactone

CAS No. 147795-39-9

N-3-Oxo-octanoyl-L-homoserine lactone( —— )

Catalog No. M28355 CAS No. 147795-39-9

N-3-Oxo-octanoyl-L-homoserine lactone, a quorum-sensing signal, is an Agrobacterium autoinducer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    N-3-Oxo-octanoyl-L-homoserine lactone
  • Note
    Research use only, not for human use.
  • Brief Description
    N-3-Oxo-octanoyl-L-homoserine lactone, a quorum-sensing signal, is an Agrobacterium autoinducer.
  • Description
    N-3-Oxo-octanoyl-L-homoserine lactone, a quorum-sensing signal, is an Agrobacterium autoinducer.(In Vitro):N-3-Oxo-octanoyl-L-homoserine lactone (3OC8-HSL) pretreatment (10?μM; for 2?days) exerts strong inhibitory effect on pathogen proliferation in the leaves. Plants treated with N-3-Oxo-octanoyl-L-homoserine lactone shows increased activities of defense-related enzymes including peroxidase, catalase, phenylalanine ammonialyase, and superoxide dismutase.
  • In Vitro
    N-3-Oxo-octanoyl-L-homoserine lactone (3OC8-HSL) pretreatment (10?μM; for 2?days) exerts strong inhibitory effect on pathogen proliferation in the leaves. Plants treated with N-3-Oxo-octanoyl-L-homoserine lactone shows increased activities of defense-related enzymes including peroxidase, catalase, phenylalanine ammonialyase, and superoxide dismutase.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Bcl-6
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    147795-39-9
  • Formula Weight
    735.8
  • Molecular Formula
    C41H42FN5O7
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (414.46 mM)
  • SMILES
    Cc(cc1)cnc1C1=CN(CC2CCOCC2)C=C(C(Nc(cc2)cc(F)c2-c2c(N)ncc(-c(cc3)cc(OC)c3OC[C@@H]3OCCOC3)c2)=O)C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Guo W, et al. Synthesis and Biological Evaluation of B-Cell Lymphoma 6 Inhibitors of N-Phenyl-4-pyrimidinamine Derivatives Bearing Potent Activities against Tumor Growth. J Med Chem. 2020;63(2):676-695.
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