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: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid
    Order number: 204513
    CAS: 1211504-14-1
    Purity: >=95%
    Appearance: solid
    MF: C30H37NO4
    MW: 475.629
    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)-2-(2'-Propylenyl)alanine
    Order number: 204514
    CAS: 96886-55-4
    Purity: >=95%
    Appearance: solid
    MF: C6H11NO2
    MW: 129.159
    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)-2-(2'-Propylenyl)alanine
    Order number: 204515
    CAS: 96886-56-5
    Purity: >=95%
    Appearance: solid
    MF: C6H11NO2
    MW: 129.159
    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)-2-(3'-Butenyl)alanine
    Order number: 204516
    CAS: 1011309-60-0
    Purity: >=95%
    Appearance: solid
    MF: C7H13NO2
    MW: 143.186
    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)- 2-(3'-Butenyl)alanine
    Order number: 204517
    CAS: na
    Purity: >=95%
    Appearance: solid
    MF: C7H13NO2
    MW: 143.186
    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)- 2-(5'-Pentenyl)alanine
    Order number: 204518
    CAS: 1011309-61-7
    Purity: >=95%
    Appearance: solid
    MF: C8H15NO2
    MW: 157.213
    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.