BZAD01

CAS No. 305339-41-7

BZAD01( BZAD-01 | BZAD 01 )

Catalog No. M27808 CAS No. 305339-41-7

BZAD01 is a selective NMDA NR1A/2B receptor antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 44 In Stock
5MG 30 In Stock
10MG 50 In Stock
25MG 102 In Stock
50MG 155 In Stock
100MG 258 In Stock
200MG 359 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    BZAD01
  • Note
    Research use only, not for human use.
  • Brief Description
    BZAD01 is a selective NMDA NR1A/2B receptor antagonist.
  • Description
    BZAD01 is a selective NMDA NR1A/2B receptor antagonist.(In Vivo):Parkinsonism was induced by microinjection of the toxin, 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle (MFB) of 40 Sprague-Dawley rats. Parkinsonism and the efficacy of drugs were assessed using a battery of behavioural tests including balance beam, apomorphine-induced rotation, body axis bias or "curling", head position bias and disengage sensorimotor latency test. The main effects were that BZAD01 co-administration prevented chronic levodopa-induced potentiation of apomorphine rotation. However levodopa-treated rats were slower than either controls or BZAD-01-treated rats in the locomotor test.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    BZAD-01 | BZAD 01
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    NMDAR
  • Recptor
    Guanylate cyclase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    305339-41-7
  • Formula Weight
    362.275
  • Molecular Formula
    C16H12F6N2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?Methanol : 250 mg/mL (690.09 )
  • SMILES
    FC(F)(F)Oc1ccc(cc1)C(=N)NCc1ccccc1C(F)(F)F
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Barbara ALBRECHT-KüPPER, et al. Selective partial adenosine a1 receptor agonists in combination with soluble guanylyl cyclase (sgc) stimulators and/or activators. WO2018153899A1.
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