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Chemical Structure| 1392116-14-1 Chemical Structure| 1392116-14-1

Structure of JD-5037
CAS No.: 1392116-14-1

Chemical Structure| 1392116-14-1

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JD-5037 is an effective antagonist of CB1R with an IC50 value of 1.5 nM.

Synonyms: JD-5037

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Product Details of JD-5037

CAS No. :1392116-14-1
Formula : C27H27Cl2N5O3S
M.W : 572.51
SMILES Code : CC(C)[C@H](/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)C(N)=O
Synonyms :
JD-5037
MDL No. :MFCD30533451
InChI Key :GTCSIQFTNPTSLO-RPWUZVMVSA-N
Pubchem ID :66553204

Safety of JD-5037

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Related Pathways of JD-5037

GPCR

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
MGN3-1 cells 100 nM 6 h To study the effect of JD5037 on fatty acid uptake and processing in MGN3-1 cells, results showed that JD5037 significantly increased the uptake of [2H31]palmitic acid and the generated labeled acyl-carnitine species. PMC6551287
3T3 L1 adipocytes 100 nM 24 h JD5037 reversed CB1R agonist-induced increases in leptin secretion PMC3832894
HepG2 cells 10 μM 1 h To study the effect of JD-5037 on insulin signaling, results showed that JD-5037 could block the inhibition of insulin-induced akt phosphorylation. PMC3839256
Mouse primary hepatocytes 10 μM To study the effect of JD-5037 on ceramide synthesis, results showed that JD-5037 could block ceramide synthesis. PMC3839256
HepG2 cells 100 nM overnight JD5037 reversed the inhibitory effects of ACEA on insulin-induced Akt phosphorylation, indicating that the Sirt1/mTORC2/Rictor signaling pathway plays a key role in the reversal of insulin signaling inhibition by CB1R antagonists. PMC6438767
Primary mouse hepatocytes 100 nM 25 h JD5037 reversed the inhibitory effects of ACEA on Sirt1 and Rictor expression, indicating that the CB1R antagonist reversed the inhibition of insulin signaling via the Sirt1/mTORC2 pathway. PMC6438767
HepG2 cells 1–5 μM 1 h To analyze the mechanism of CB1R-dependent FOXM1 expression, results showed that AEA significantly induced FOXM1 expression, and this induction was blocked by pertussis toxin. PMC4406817
Bone marrow-derived macrophages (BMDMs) 1 µM 24 h To study the effect of CB1 agonist ACEA on BMDM proliferation, results showed that ACEA increased BMDM proliferation. PMC11481387
Bone marrow-derived macrophages (BMDMs) 10 µM 24 h To study the effect of CB1 antagonist AM281 on BMDM proliferation, results showed that AM281 inhibited BMDM proliferation. PMC11481387
Human islet cells 10 nM 6 days To investigate the effect of JD-5037 on insulitis, results showed that JD-5037 significantly reduced cytokine-induced accumulation and immune cell infiltration into islets. PMC11410908

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice C57BL/6J mice Oral 3 mg/kg Once daily for 5 days To study the effect of JD5037 on alcohol intake and preference in mice, results showed that JD5037 significantly reduced ethanol intake and preference. PMC6551287
Mice Diet-induced obese mice Oral 3 mg/kg Daily for 28 days JD5037 reduced food intake,, and adiposity, and reversed leptin resistance PMC3832894
Mice High-fat diet-induced obese mice Intraperitoneal injection 3 mg/kg Once daily for 28 days To study the effect of JD-5037 on, steatosis, glucose tolerance, and insulin sensitivity in obese mice, results showed that JD-5037 could reduce, improve steatosis, enhance glucose tolerance, and increase insulin sensitivity. PMC3839256
Mice High-fat diet-induced obese mice Oral gavage 3 mg/kg Daily for 2 or 4 weeks JD5037 treatment reversed the HFD-induced suppression of Sirt1/mTORC2 signaling, improved insulin sensitivity and glycemic control, and increased fatty acid oxidation and energy expenditure. PMC6438767
Mice DEN-induced liver cancer model Oral gavage 3 mg/kg Once daily for 8 weeks To evaluate the inhibitory effect of JD5037 on DEN-induced liver cancer, results showed that JD5037 significantly reduced tumor volume. PMC4406817
Mice Atherosclerosis model Intraperitoneal injection 3 mg/kg Daily for 4 weeks To study the effect of peripheral CB1 antagonist JD5037 on atherosclerosis plaque progression, results showed that JD5037 inhibited plaque progression and reduced macrophage accumulation and proliferation in male mice. PMC11481387
Mice NOD mice Intraperitoneal injection 3 mg/kg Once daily for 1 week To investigate the effect of JD-5037 on insulitis, results showed that JD-5037 significantly prevented immune cell infiltration into the islets. PMC11410908
Mice Magel2-null mice Intraperitoneal injection 3 mg/kg Once daily for 28 days JD5037, through peripheral CB1 receptor antagonism, reversed the obese phenotype in Magel2-null mice, reduced hyperphagia, and improved metabolic parameters. PMC5123200
Mice CCl4-induced fibrotic liver model Oral 3 mg/kg Once daily for 8 weeks To investigate the inhibitory effect of JD-5037 on liver fibrosis, results showed that JD-5037 attenuated liver fibrosis by blocking the CB1 receptor/β-arrestin1/Akt signaling pathway. PMC7236068
Mice Mdr2−/− mice Oral gavage 3 mg/kg Every other day for 4 weeks JD5037 significantly exacerbated liver injury in Mdr2?/? mice, evidenced by elevated serum ALT and ALP levels and exacerbated liver histology. JD5037-treated Mdr2?/? mice exhibited significantly heightened serum bile acid levels. JD5037 treatment intensified liver fibrosis, increased fibrogenic gene expression, stimulated ductular reaction, and upregulated hepatic proinflammatory cytokines. PMC11240654

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.75mL

0.35mL

0.17mL

8.73mL

1.75mL

0.87mL

17.47mL

3.49mL

1.75mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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