Amino Acids, Nucleosides and Nucleotides

Amino Acids

We offer Fmoc-protected unnatural amino acids for the synthesis of peptides for biological research and pharmaceutical development. By introducing conformational constraints, the peptides may have one or several of the following features: 1. enhancement of peptide backbone helicity for better target binding; 2. tunable hydrophobicity for desired cellular permeability and cytotoxicity; and 3. enhancement of peptide stability against proteolytic breakdown.

Nucleosides and Nucleoside Phosphoramidites

We offer nucleosides with modifications in both the nucleic acid base and the sugar component of the molecules. Nucleoside phosphoramidites are extremely useful chemical building blocks for the chemical synthesis of RNA-targeting drugs such as antisense oligonucleotides, aptamers, and siRNAs which have exhibited promises for treating diseases including muscular dystrophy, neuropathies, and macular degeneration.

Nucleotides

dNTP, NTP, and modified nucleotides have exhibited a wide range of applications in PCR, RT-PCR, cRNA synthesis, RCA, MDA, DNA labeling, and sequencing. dNTPs are chemical building blocks in the commercial manufacture of mRNA vaccines using in vitro transcription method.

Inquire about our bulk quantities for the manufacture of oligonucleotide drug ingredients and large-scale production of mRNAs.

  • Amino Acids for Stapled Peptides
  • 2-Methylated Amino Acids
  • Peptide Labeling
  • Other Unnatural Amino Acids
  • Nucleosides
  • HNA Precursors
  • Morpholino Nucleosides
  • Nucleoside Phosphoramidites and Nucleotides
  • Amino Acids for Stapled Peptides

    Structure Details
    Product Name: (S)-N-Fmoc-2-(5'-hexenyl)alanine
    Order number: 204463
    CAS: 288617-74-3
    Purity: >=95%
    Appearance: solid
    MF: C24H27NO4
    MW: 393.483
    MP: n.a. oC

    Description:
    This alpha-methylated amino acid is used to make the peptide bond more stable against enzymatic hydrolysis. Helicity can be locked via Grubbs' methathesis reaction.
    Product Name: (R)-N-Fmoc-2-(5'-hexenyl)alanine
    Order number: 204464
    CAS: 288617-78-7
    Purity: >=95%
    Appearance: solid
    MF: C24H27NO4
    MW: 393.483
    MP: n.a. oC

    Description:
    This alpha-methylated amino acid is used to make the peptide bond more stable against enzymatic hydrolysis. Helicity can be locked via Grubbs' methathesis reaction.
    Product Name: (S)-N-Fmoc-2-(6'-heptenyl)alanine
    Order number: 204465
    CAS: 1311933-83-1
    Purity: >=95%
    Appearance: solid
    MF: C25H29NO4
    MW: 407.51
    MP: n.a. oC

    Description:
    This alpha-methylated amino acid is used to make the peptide bond more stable against enzymatic hydrolysis. Helicity can be locked via Grubbs' methathesis reaction.
    Product Name: (S)-N-Fmoc-allyl-glycine
    Order number: 204467
    CAS: 146549-21-5
    Purity: >=95%
    Appearance: solid
    MF: C20H19NO4
    MW: 337.375
    MP: n.a. oC

    Description:
    The alkenyl side chain of this product can be tied (stapled) with another adjacent alkenyl side chain pre-existed on the peptide backbone via a ring-closure metathesis process.
    Product Name: (R)-N-Fmoc-allyl-glycine
    Order number: 204468
    CAS: 170642-28-1
    Purity: >=95%
    Appearance: solid
    MF: C20H19NO4
    MW: 337.375
    MP: n.a. oC

    Description:
    The alkenyl side chain of this product can be tied (stapled) with another adjacent alkenyl side chain pre-existed on the peptide backbone via a ring-closure metathesis process.
    Product Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hex-5-enoic acid
    Order number: 204469
    CAS: 851909-08-5
    Purity: >=95%
    Appearance: solid
    MF: C21H21NO4
    MW: 351.402
    MP: n.a. oC

    Description:
    The alkenyl side chain of this product can be tied (stapled) with another adjacent alkenyl side chain pre-existed on the peptide backbone via a ring-closure metathesis process.