J-2156

Modify Date: 2024-01-10 19:16:42

J-2156 Structure
J-2156 structure
Common Name J-2156
CAS Number 848647-56-3 Molecular Weight 468.57
Density N/A Boiling Point N/A
Molecular Formula C24H28N4O4S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of J-2156


J-2156 is a high potent, selective somatostatin receptor type 4 (SST4 receptor) agonist with IC50s of 0.05 nM and 0.07 nM for human and rat SST4 receptors, respectively. The ED50 of J-2156 in rats for the relief of mechanical allodynia and mechanical hyperalgesia in the ipsilateral hindpaws was 3.7 and 8.0 mg/kg, respectively[1].

 Names

Name J-2156

 J-2156 Biological Activity

Description J-2156 is a high potent, selective somatostatin receptor type 4 (SST4 receptor) agonist with IC50s of 0.05 nM and 0.07 nM for human and rat SST4 receptors, respectively. The ED50 of J-2156 in rats for the relief of mechanical allodynia and mechanical hyperalgesia in the ipsilateral hindpaws was 3.7 and 8.0 mg/kg, respectively[1].
Related Catalog
Target

IC50: 0.05 nM (human SST4) and 0.07 nM (rat SST4)[1]

In Vivo J-2156 (1-10 mg/kg; i.p.; for 3 hours) of single bolus doses has anti-allodynic effect on ipsilateral and contralateral in BCIBP-rats[1]. Animal Model: BCIBP-rats[1] Dosage: 1, 3, 10 mg/kg Administration: I.p.; for 3 hours Result: Had anti-allodynic effect on ipsilateral and contralateral in BCIBP-rats.
References

[1]. Shenoy PA, et al. The Somatostatin Receptor-4 Agonist J-2156 Alleviates Mechanical Hypersensitivity in a Rat Model of Breast Cancer Induced Bone Pain. Front Pharmacol. 2018 May 15;9:495.

 Chemical & Physical Properties

Molecular Formula C24H28N4O4S
Molecular Weight 468.57