L-Selenocystine

CAS No. 29621-88-3

L-Selenocystine( —— )

Catalog No. M28015 CAS No. 29621-88-3

L-Selenocystine can be used as a building block in biologically active selenol compounds.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 48 In Stock
25MG 29 In Stock
50MG 35 In Stock
100MG 50 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    L-Selenocystine
  • Note
    Research use only, not for human use.
  • Brief Description
    L-Selenocystine can be used as a building block in biologically active selenol compounds.
  • Description
    L-Selenocystine can be used as a building block in biologically active selenol compounds.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Antiviral
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    29621-88-3
  • Formula Weight
    334.114
  • Molecular Formula
    C6H12N2O4Se2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 5.88 mg/mL (17.60 mMu)
  • SMILES
    N[C@@H](C[Se][Se]C[C@H](N)C(O)=O)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Xie S, et al. Magnetic-assisted biotinylated single-chain variable fragment antibody-based immunoassay for amantadine detection in chicken. Anal Bioanal Chem. 2018 Sep;410(24):6197-6205.
molnova catalog
related products
  • [Pro3]-GIP (Rat)

    High affinity rat GIP receptor partial agonist (Kd = 13 nM). Increases cAMP accumulation in COS-7 cells transfected with rat GIP receptor, while also acting as a competitive antagonist of GIP.

  • MC1742

    MC1742 is an inhibitor of class I histone deacetylases (HDACs; IC50s = 0.1, 0.11, 0.02, and 0.61 μM for HDAC1, -2, -3, and -8, respectively) and class IIb HDACs (IC50s = 7 and 40 nM for HDAC6 and HDAC10, respectively).

  • FG 7142

    FG 7142?also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM).?FG 7142?can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex.?FG 7142 , a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM).?