H4 Receptor antagonist 1

CAS No. 848217-00-5

H4 Receptor antagonist 1( —— )

Catalog No. M20493 CAS No. 848217-00-5

H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist with an IC50 of 19 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 38 In Stock
5MG 34 In Stock
10MG 53 In Stock
25MG 106 In Stock
50MG 179 In Stock
100MG 259 In Stock
200MG 365 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    H4 Receptor antagonist 1
  • Note
    Research use only, not for human use.
  • Brief Description
    H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist with an IC50 of 19 nM.
  • Description
    H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist with an IC50 of 19 nM.
  • In Vitro
    H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist, with an IC50 of 19 nM.
  • In Vivo
    H4 Receptor antagonist 1 indicates that metabolic stability in rat microsomes is very low with only 1% parent compound remaining after 10 min incubation.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Histamine Receptor
  • Recptor
    H4 receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    848217-00-5
  • Formula Weight
    316.78
  • Molecular Formula
    C16H17ClN4O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mg/mL (31.57 mM)
  • SMILES
    CN1CCN(CC1)c1nc(C)nc2c3cc(Cl)ccc3oc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Cramp S Dyke H J Higgs C et al. Identification and hit-to-lead exploration of a novel series of histamine H4 receptor inverse agonists[J]. Bioorganic & Medicinal Chemistry Letters 2010 20(8):2516-2519.
molnova catalog
related products
  • JNJ-18038683

    JNJ-18038683 is a potent, selective 5-HT7 receptor antagonist with pKi of 8.19 and 8.20 for rat and human 5-HT7 in cell-based assays; decreases 5-HT (100 nM)-stimulated adenylyl cyclase in rat and human 5-HT7/HEK293 cells with pKb of 8.01 and 7.99, respectively.

  • Noberastine

    Noberastine (R 64947) is a novel histamine H1 antagonist with potent and specific peripheral antihistamine activity.

  • Conessine

    Conessine, a steroidal alkaloid isolated from Holarrhena floribunda, interacts with the histamine H3 receptor and has anti-malarial activity.