Fmoc-Thr(GlcNAc(Ac)3-b-D)-OH

CAS No. 160168-40-1

Fmoc-Thr(GlcNAc(Ac)3-b-D)-OH ( —— )

Catalog No. M21715 CAS No. 160168-40-1

This amino acid is compatible with standard protocols in Fmoc solid phase peptide synthesis.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 276 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Fmoc-Thr(GlcNAc(Ac)3-b-D)-OH
  • Note
    Research use only, not for human use.
  • Brief Description
    This amino acid is compatible with standard protocols in Fmoc solid phase peptide synthesis.
  • Description
    This amino acid is compatible with standard protocols in Fmoc solid phase peptide synthesis. Following chain assembly, removal of the acetyl protecting group can be carried out by treatment of the peptidyl resin with methanolic ammonia or sodium methoxide/DMF/methanol, or by treatment of the cleaved peptide with catalytic sodium methoxide in methanol.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    160168-40-1
  • Formula Weight
    670.66
  • Molecular Formula
    C33H38N2O13
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • ms48107

    MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). It is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. It can readily cross the blood-brain barrier (BBB) in mice.

  • Integerrimine N-oxid...

    The herbs of Senecio scandens.

  • Dehydrovomifoliol

    Dehydrovomifoliol could be a marker of Polish heather honey. Dehydrovomifoliol exhibits moderate acetylcholinesterase (AChE) inhibitory activities.