Cart
sales@molnova.com
Home - Products - GPCR/G Protein - Calcium Channel - Cinacalcet metabolite M4

Cinacalcet metabolite M4

CAS No. 104774-87-0

Cinacalcet metabolite M4( Rarechem AL BW 1078 )

Catalog No. M26115 CAS No. 104774-87-0

Cinacalcet metabolite M4 is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 45 Get Quote
10MG 61 Get Quote
25MG 87 Get Quote
50MG 125 Get Quote
100MG 161 Get Quote
200MG 230 Get Quote
500MG 346 Get Quote
1G Get Quote Get Quote
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    Cinacalcet metabolite M4
  • Note
    Research use only, not for human use.
  • Brief Description
    Cinacalcet metabolite M4 is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
  • Description
    Cinacalcet metabolite M4 is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Rarechem AL BW 1078
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    104774-87-0
  • Formula Weight
    203.208
  • Molecular Formula
    C10H12F3N
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    NCCCc1cccc(c1)C(F)(F)F
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.J.L.M.Heeremans, et al. Interference of ?-amino-caproic acid with [N-succinimidyl S-acetylthioacetate derived] thiol-introduction into glu-plasminogen. Volume 8, Supplement 2, 1994, Pages 138-141.
Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • DS16570511

    DS16570511 is a cellular osmotic inhibitor of mitochondrial calcium monoab, which blocks MCU or MICU1-dependent Ca2+ influx.DS16570511 dose - dependent inhibition of serum-induced mitochondrial Ca2+ influx in HEK293A cells with IC50 of 7 M.DS16570511 inhibits the uptake of isolated Ca2+. mitochondria from human cells, rat heart and pig heart.

  • (±)-Liquiritigenin

    (±)-Liquiritigenin ((±)-4',7-Dihydroxyflavanone), a flavonoid extracted from Angelica keiskei, inhibits the calcium-activated chloride channel TMEM16A.(±)-Liquiritigenin induces an increase in apoptosis and an enhancement of caspase3 activity.

  • MK-8998

    MK-8998 (CX-8998) is a potent and selective antagonist of the T-type calcium channel for the treatment of schizophrenia.

Sign In Join Free