(-)-Camphoric acid

CAS No. 560-09-8

(-)-Camphoric acid( Camphoric acid, (-)- | L-Camphoric acid )

Catalog No. M27237 CAS No. 560-09-8

(-)-Camphoric acid is a less active enantiomer of Camphoric acid which induces GluR expression.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG 37 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    (-)-Camphoric acid
  • Note
    Research use only, not for human use.
  • Brief Description
    (-)-Camphoric acid is a less active enantiomer of Camphoric acid which induces GluR expression.
  • Description
    (-)-Camphoric acid is a less active enantiomer of Camphoric acid which induces GluR expression.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Camphoric acid, (-)- | L-Camphoric acid
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    PFKFB3
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    560-09-8
  • Formula Weight
    200.23
  • Molecular Formula
    C10H16O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (624.28 mM)
  • SMILES
    O=C([C@]1(C)C(C)(C)[C@H](C(O)=O)CC1)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Minsuh Seo, et al. Structure-based development of small molecule PFKFB3 inhibitors: a framework for potential cancer therapeutic agents targeting the Warburg effect. PLoS One. 2011;6(9):e24179.
molnova catalog
related products
  • A-794282

    A-794282 is a selective and potent mGlu1 receptor antagonist with analgesic activity and may be useful in the study of neurologic disorders.

  • VU0422288

    VU0422288 (ML396) is a potent orthosteric modulator of type III mGlu receptors (mGlus).VU0422288 shows inhibition of mGluR4, mGluR7, and mGluR8 in a calcium mobilization assay.

  • CPCCOEt

    CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b.