Accueil>>Signaling Pathways>> GPCR/G protein>> Adenosine Receptor>>A2AR-agonist-1

A2AR-agonist-1 (Synonyms: JMF 1907)

Catalog No.GC30987

A2AR-agonist-1 est un puissant agoniste A2AR et ENT1 avec Ki de 4,39 et 3,47 pour A2AR et ENT1.

Products are for research use only. Not for human use. We do not sell to patients.

A2AR-agonist-1 Chemical Structure

Cas No.: 41552-95-8

Taille Prix Stock Qté
10mM (in 1mL DMSO)
354,00 $US
En stock
5mg
321,00 $US
En stock
10mg
459,00 $US
En stock
50mg
1 379,00 $US
En stock
100mg
1 930,00 $US
En stock

Tel:(909) 407-4943 Email: sales@glpbio.com

Avis des clients

Based on customer reviews.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

A2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) [1]Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine Transporter for Neuroprotection.[1]

[1]. Chen JB, et al. Design and synthesis of novel dual-action compounds targeting the adenosine A(2A) receptor and adenosine transporter for neuroprotection. ChemMedChem. 2011 Aug 1;6(8):1390-1400. [2]. Lin Yun-Lian, et al. Dual-action compounds targeting adenosine A2A receptor and adenosine transporter for prevention and treatment of neurodegenerative diseases. From PCT Int. Appl. (2012), WO 2012064340 A1 20120518. [3]. Chen, Chih-Cheng, et al. Methods and compositions for treating pain. From PCT Int. Appl. (2013), WO 2013120078 A1 20130815.

Avis

Review for A2AR-agonist-1

Average Rating: 5 ★★★★★ (Based on Reviews and 22 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for A2AR-agonist-1

GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.

Required fields are marked with *

You may receive emails regarding this submission. Any emails will include the ability to opt-out of future communications.