RU-24969

CAS No. 66611-26-5

RU-24969( RU24969 | RU 24969 )

Catalog No. M15539 CAS No. 66611-26-5

A potent, selective agonist of 5-HT1A and 5-HT1B receptors, with preference for 5-HT1B.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 63 In Stock
5MG 53 In Stock
10MG 81 In Stock
50MG 257 In Stock
100MG 383 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    RU-24969
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective agonist of 5-HT1A and 5-HT1B receptors, with preference for 5-HT1B.
  • Description
    A potent, selective agonist of 5-HT1A and 5-HT1B receptors, with preference for 5-HT1B; inhibited the rate of synthesis of 5-HT in rat brain by about 50% (10mg/kg)
  • In Vitro
    RU 24969 (10 μM) reduces K+-stimulated release of [3H]-5-HT from ratfrontalcortex slices in vitro.
  • In Vivo
    RU 24969 (0.03-3.0 mg/kg; s.c.) dose-dependently decreases water consumption in water deprived rats.RU 24969 (0.3-3.0 mg/kg; s.c.) dose-dependently increases forward locomotion. Animal Model:Male Sprague-Dawley rats Dosage:0.03, 0.3, 1.0, 3.0 mg/kg Administration:A single s.c.Result:Decreased water consumption significantly at dose of 0.3, 1.0, and 3.0 mg/kg.
  • Synonyms
    RU24969 | RU 24969
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT Receptor
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    66611-26-5
  • Formula Weight
    228.2896
  • Molecular Formula
    C14H16N2O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 30 mg/mL
  • SMILES
    COC1=CC2=C(NC=C2C3=CCNCC3)C=C1
  • Chemical Name
    1H-Indole, 5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-

Shipping & Storage Information

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

Reference

1. Green AR, et al. Neuropharmacology. 1984 Jun;23(6):655-61. 2. Harrison AA, et al. Psychopharmacology (Berl). 1999 Jan;141(3):242-50. 3. Parsons LH, et al. J Neurosci. 1998 Dec 1;18(23):10078-89.
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