Product Details
Product Name:
JZL195 |
CAS No.:
1210004-12-8 |
Purity:
99.81% |
Supply Ability:
10g |
Release date:
2024/11/19 |
Product Introduction
Bioactivity
Name | JZL195 |
Description | JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor. |
In vitro | In the corpora cavernosa of rats with Type 2 Diabetes Mellitus (T2DM), the injection of Avanafil (1 μM) has been shown to improve erectile dysfunction. |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
Solubility Information | DMSO : 11 mg/mL (25.38 mM), Sonication is recommended.
|
Keywords | Autophagy | Monoacylglycerol lipase | JZL 195 | inhibit | JZL195 | MAGL | JZL-195 | Fatty acid amide hydrolase | Inhibitor | FAAH |
Inhibitors Related | Stavudine | Xylitol | Myricetin | Sodium 4-phenylbutyrate | Hydroxychloroquine | Guanidine hydrochloride | Taurine | Curcumin | Oxyresveratrol | Paeonol | Naringin | Gefitinib |
Related Compound Libraries | Target-Focused Phenotypic Screening Library | Bioactive Compound Library | Neuronal Signaling Compound Library | Anti-Obesity Compound Library | Autophagy Compound Library | Inhibitor Library | Lipid Metabolism Compound Library | Bioactive Compounds Library Max | Bioactive Lipid Compound Library | Anti-COVID-19 Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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