Fmoc-Ser-OMe

• Description:

  Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor[1][2].

• Product Name Alternative:

  Fmoc-L-Ser-OMe

• UNSPSC:

  12352209

• Hazard Statement:

  H302, H315, H319, H335

• Target:

  Amino Acid Derivatives

• Type:

  Peptides

• Related Pathways:

  Others

• Field of Research:

  Others

• Assay Protocol:

  https://www.medchemexpress.com/fmoc-ser-ome.html

• Purity:

  99.71

• Solubility:

  DMSO : 200 mg/mL (ultrasonic)

• Smiles:

  OC[C@@H](C(OC)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O

• Molecular Formula:

  C19H19NO5

• Molecular Weight:

  341.36

• Precautions:

  H302, H315, H319, H335

• References & Citations:

  [1]Tamiaki H, et al. Synthesis of chlorophyll-amino acid conjugates as models for modification of proteins with chromo/fluorophores. Bioorg Med Chem. 2014 Feb 15;22 (4) :1421-8. |[2]Kärkkäinen TS, et al. Iodine-mediated glycosylation en route to mucin-related glyco-aminoacids and glycopeptides. Carbohydr Res. 2008 Jul 21;343 (10-11) :1830-4.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category:

  Peptides

• Clinical Information:

  No Development Reported

• CAS Number:

  82911-78-2