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AZD1979
🥰Excellent
Catalog No. T14372Cas No. 1254035-84-1
Alias AZD 1979
AZD1979 is a highly potent MCHR1 (Melanin-concentrating hormone receptor 1) antagonist with an IC50 of 12 nM, exhibiting improved central nervous system (CNS) exposure and enhanced insulin sensitivity in steady-state model assessments, making it suitable for the treatment of obesity.
AZD1979
🥰Excellent
Purity: 99.72%
Catalog No. T14372Alias AZD 1979Cas No. 1254035-84-1
AZD1979 is a highly potent MCHR1 (Melanin-concentrating hormone receptor 1) antagonist with an IC50 of 12 nM, exhibiting improved central nervous system (CNS) exposure and enhanced insulin sensitivity in steady-state model assessments, making it suitable for the treatment of obesity.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $82 | In Stock | |
| 5 mg | $198 | In Stock | |
| 10 mg | $358 | In Stock | |
| 25 mg | $769 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $219 | In Stock |
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Purity:99.72%
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Product Introduction
Bioactivity
Chemical Properties
| Description | AZD1979 is a highly potent MCHR1 (Melanin-concentrating hormone receptor 1) antagonist with an IC50 of 12 nM, exhibiting improved central nervous system (CNS) exposure and enhanced insulin sensitivity in steady-state model assessments, making it suitable for the treatment of obesity. |
| Targets&IC50 | MCHr1:~12 nM |
| In vivo | Method: AZD1979 was administered orally once daily for several days to diet-induced obese (DIO) mice. Body weight, food intake, fasting blood glucose, and insulin levels were monitored to evaluate its effects on energy metabolism. Result: AZD1979 dose-dependently reduced body weight and food intake, and significantly improved fasting glucose and insulin levels, indicating a beneficial role in metabolic regulation. [1] |
| Synonyms | AZD 1979 |
| Molecular Weight | 462.5 |
| Formula | C25H26N4O5 |
| Cas No. | 1254035-84-1 |
| Smiles | O=C(C1=NN=C(O1)C=2C=CC(OC)=CC2)N3CC(OC4=CC=C(C=C4)CN5CC6(COC6)C5)C3 |
| Relative Density. | 1.41 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 30 mg/mL (64.86 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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