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Ciraparantag acetate

CAS No. 1644388-83-9

Ciraparantag acetate( Ciraparantag acetate(1438492-26-2 Free base) )

Catalog No. M26117 CAS No. 1644388-83-9

Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 104 In Stock
2MG 36 In Stock
5MG 57 In Stock
10MG 93 In Stock
25MG 188 In Stock
50MG 305 In Stock
100MG 500 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
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Biological Information

  • Product Name
    Ciraparantag acetate
  • Note
    Research use only, not for human use.
  • Brief Description
    Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.
  • Description
    Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin. It shows binding characteristics that are similar to those of direct oral anticoagulants (DOACs).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Ciraparantag acetate(1438492-26-2 Free base)
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Alkyl/ether
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1644388-83-9
  • Formula Weight
    572.75
  • Molecular Formula
    C24H52N12O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(NCCCN1CCN(CCCNC([C@@H](N)CCCNC(N)=N)=O)CC1)[C@@H](N)CCCNC(N)=N.CC(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Jiang F, et al. Discovery of novel small molecule induced selective degradation of the bromodomain and extra-terminal (BET) bromodomain protein BRD4 and BRD2 with cellular potencies.Bioorg Med Chem. 2020 Jan 1;28(1):115181.
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