3-METHOXY-DL-TYROSINE

CAS No. 7636-26-2

3-METHOXY-DL-TYROSINE( —— )

Catalog No. M28712 CAS No. 7636-26-2

3-METHOXY-DL-TYROSINE is a chemical compound.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 37 Get Quote
10MG 51 Get Quote
25MG 87 Get Quote
50MG 141 Get Quote
100MG 209 Get Quote
200MG 314 Get Quote
500MG 537 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    3-METHOXY-DL-TYROSINE
  • Note
    Research use only, not for human use.
  • Brief Description
    3-METHOXY-DL-TYROSINE is a chemical compound.
  • Description
    3-METHOXY-DL-TYROSINE is a chemical compound.
  • In Vitro
    Endogenous metabolites is defined as those that are annotated by Kyoto Encyclopedia of Genes and Genomes as substrates or products of the ~1900 metabolic enzymes encoded in our genome. It is clear in the body of literature that there are documented toxic properties for many of these metabolites.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Nek2|RSK1|DYRK1a|CHK1|GSK-3β|ABL|CDK2|CDK4|AKT1|Aurora A
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    7636-26-2
  • Formula Weight
    211.217
  • Molecular Formula
    C10H13NO4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 5 mg/mL (23.67 mM)
  • SMILES
    COc1cc(CC(N)C(O)=O)ccc1O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Xi JB, et al. Structure-based design and synthesis of imidazo[1,2-a]pyridine derivatives as novel and potent Nek2 inhibitors with in vitro and in vivo antitumor activities. Eur J Med Chem. 2017 Jan 27;126:1083-1106.
molnova catalog
related products
  • CAY10602

    CAY10602 is a SIRT1 activator. CAY10602 was derived from high throughput screening for compounds that increase SIRT1-mediated deacetylation of a SIRT1-specific substrate.

  • R715 TFA(185052-09-9...

    Potent and selective bradykinin B1 receptor antagonist (pA2 = 8.49). Displays no activity at B2 receptors. Reduces mechanical hypernociception in a mouse model of neuropathic pain. Metabolically stable.

  • 21-O-Tigloylgymnemag...

    21-O-Tigloylgymnemagenin is a natural product.