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JD5037
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
JD5037图片
CAS NO:1392116-14-1
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 572.51
Formula C27H27Cl2N5O3S
CAS No. 1392116-14-1
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 10 mM
Water: <1 mg/mL
Ethanol: <1 mg/mL
SMILESCC(C)[C@@H](C(N)=O)/N=C(N1N=C(C2=CC=C(Cl)C=C2)[C@@H](C3=CC=CC=C3)C1)/NS(=O)(C4=CC=C(Cl)C=C4)=O
Synonyms

JD-5037; JD 5037; JD5037;

Chemical Name: (S)-2-(((E)-((S)-3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazol-1-yl)((4-chlorophenyl)sulfonamido)methylene)amino)-3-methylbutanamide

Exact Mass: 571.1212

实验参考方法
In Vitro

In vitro activity: JD5037 is an inverse agonist of peripherally restricted (PR) cannabinoid 1 (CB1) receptors with Ki of 0.35 nM. Antagonists (inverse agonists) of the cannabinoid-1 (CB1) receptor showed promise as new therapies for controlling obesity and related metabolic function/liver disease. These agents, representing diverse chemical series, shared the property of brain penetration due to the initial belief that therapeutic benefit was mainly based on brain receptor interaction. JD5037 displays>700-fold selectivity for CB1 over CB2,>1,000-fold selectivity over a panel of 70 receptors, transporters, and ion channels, and low blood-brain barrier penetrance.JD5037 is orally bioavailable and reduces food intake, body weight, and hormonal/metabolic abnormalities in diet-induced obese mice.


Kinase Assay: JD-5037 is a novel, peripherally restricted CB1R antagonist with an IC50 of 1.5 nM.

In VivoJD5037 (3 mg/kg/day, p.o.) significantly reduces the size of tumors and abrogates the tumor in DEN-treated mice. JD5037 attenuates the AEA levels in HCC samples from mice. JD5037 (3 mg/kg/d, i.p.) induces equal reductions in body weight, attenuates the HFD-induced hyperglycemia, and reduces the HFD-induced hepatic injury and steatosis in obese Magel2-null mice
Animal model Obesity mice
Formulation & Dosage JD-5037 is formulated in vehicle (V; 1% Tween80, 4% DMSO, 95% Saline); 3 mg/kg, i.p.
References Bioorg Med Chem Lett. 2013 Sep 1;23(17):4751-60