Bevenopran

CAS No. 676500-67-7

Bevenopran( CB-5945 | ADL-5945 )

Catalog No. M26628 CAS No. 676500-67-7

Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 145 In Stock
5MG 132 In Stock
10MG 198 In Stock
25MG 316 In Stock
50MG 421 In Stock
100MG 551 In Stock
200MG 728 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Bevenopran
  • Note
    Research use only, not for human use.
  • Brief Description
    Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
  • Description
    Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.(In Vivo):Bevenopran tends to increase bowel movement (BM) frequency, especially for 0.1 mg twice daily and 4 mg daily, respectively.
  • In Vitro
    ——
  • In Vivo
    Bevenopran is a peripheral μ-opioid receptor antagonist. Bevenopran is currently under investigation for the treatment of opioid-induced bowel dysfunction (OBD). Bevenopran tends to increase bowel movement (BM) frequency, especially for 0.1 mg twice daily and 4 mg daily, respectively.
  • Synonyms
    CB-5945 | ADL-5945
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    Acidic mammalian chitinase (AMCase)| Chitotriosidase (CHIT1)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    676500-67-7
  • Formula Weight
    386.452
  • Molecular Formula
    C20H26N4O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (323.47 mM)
  • SMILES
    COc1cc(CNCCC2CCOCC2)ccc1Oc1cnc(cn1)C(N)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Robert Koralewski, et al. Discovery of OATD-01, a First-in-Class Chitinase Inhibitor as Potential New Therapeutics for Idiopathic Pulmonary Fibrosis. J Med Chem. 2020 Dec 24;63(24):15527-15540.
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