Structure of JD-5037
CAS No.: 1392116-14-1
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
JD-5037 is an effective antagonist of CB1R with an IC50 value of 1.5 nM.
Synonyms: JD-5037
4.5
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
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 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
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 |
Tags: JD-5037 | JD5037 | JD 5037 | Cannabinoid Receptor | CB1 receptor antagonist | cannabinoid receptor 1 blocker | endocannabinoid system | Parkinson's disease | multiple sclerosis | cannabinoid receptors | 1392116-14-1
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P378 | |
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H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
H261 | In contact with water releases flammable gas |
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Health hazards | |
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H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
H330 | Fatal if inhaled |
H331 | Toxic if inhaled |
H332 | Harmful if inhaled |
H333 | May be harmful if inhaled |
H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
H335 | May cause respiratory irritation |
H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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