TRPV4 agonist-1 free base

CAS No. 2314467-59-7

TRPV4 agonist-1 free base( OUN67600 )

Catalog No. M24056 CAS No. 2314467-59-7

TRPV4 agonist-1 free base is an agonist of transient receptor potential vanilloid 4 (TRPV4;EC50 of 60 nM, in the hTRPV4 Ca2+ assay).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 73 In Stock
2MG 33 In Stock
5MG 56 In Stock
10MG 89 In Stock
25MG 179 In Stock
50MG 277 In Stock
100MG 384 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    TRPV4 agonist-1 free base
  • Note
    Research use only, not for human use.
  • Brief Description
    TRPV4 agonist-1 free base is an agonist of transient receptor potential vanilloid 4 (TRPV4;EC50 of 60 nM, in the hTRPV4 Ca2+ assay).
  • Description
    TRPV4 agonist-1 free base is an agonist of transient receptor potential vanilloid 4 (TRPV4;EC50 of 60 nM, in the hTRPV4 Ca2+ assay).
  • In Vitro
    TRPV4 agonist-1 (Compound 36) exhibits significantly increased potency (ECmax: 20 nM in the SOX9 reporter assay). TRPV4 agonist-1 is inactive against TRPV1 channels.
  • In Vivo
    ——
  • Synonyms
    OUN67600
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    TRP/TRPV Channel
  • Recptor
    TRPV4
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2314467-59-7
  • Formula Weight
    448.46
  • Molecular Formula
    C25H22F2N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:83.33 mg/mL?(185.81 mM;?Need ultrasonic)
  • SMILES
    CN1CCN(CC1)C2=NC3=C(C=CC=C3F)C(=O)N2C4=CC=C(C=C4)OC5=CC=C(C=C5)F
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Atobe M, et al. Discovery of Novel Transient Receptor Potential Vanilloid 4 (TRPV4) Agonists as Regulators of Chondrogenic Differentiation: Identification of Quinazolin-4(3 H)-ones and in Vivo Studies on a Surgically Induced Rat Model of Osteoarthritis. J Med Chem. 2019 Jan 28.
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