Cas no 211110-63-3 (Sobetirome)
Sobetirome Chemical and Physical Properties
Names and Identifiers
-
- Acetic acid, [4-[[4-hydroxy-3-(1-methylethyl)phenyl]methyl]-3,5-dimethylphenoxy]-
- 2-?[4-?[[4-?hydroxy-?3-?(1-?methylethyl)?phenyl]?methyl]?-?3,?5-?dimethylphenoxy]?acetic acid
- 2-[4-[(4-hydroxy-3-propan-2-ylphenyl)methyl]-3,5-dimethylphenoxy]acetic acid
- GC 1
- QRX 431
- Sobetirome
- {4-[4-hydroxy-3-(propan-2-yl)benzyl]-3,5-dimethylphenoxy}acetic acid
- acetic acid, 2-[4-[[4-hydroxy-3-(1-methylethyl)phenyl]methyl]-3,5-dimethylphenoxy]-
- GC-1
- QRX-431
- 2-[4-[[4-Hydroxy-3-(1-methylethyl)phenyl]methyl]-3,5-dimethylphenoxy]acetic acid
- 3,5-Dimethyl-4-(4′-hydroxy-3′-isopropylbenzyl)phenoxyacetic acid
- GC 1 (pharmaceutical)
- [3,5-Dimethyl-4-(4-hydroxy-3-isopropylbenzyl)phenoxy]acetic acid
- GC-1;Acetic acid,[4-[[4-hydroxy-3-(1-methylethyl)phenyl]methyl]-3,5-dimethylphenoxy]-
-
- Inchi: 1S/C20H24O4/c1-12(2)17-9-15(5-6-19(17)21)10-18-13(3)7-16(8-14(18)4)24-11-20(22)23/h5-9,12,21H,10-11H2,1-4H3,(H,22,23)
- InChI Key: QNAZTOHXCZPOSA-UHFFFAOYSA-N
- SMILES: OC1=CC=C(C=C1C(C)C)CC1C(C)=CC(=CC=1C)OCC(=O)O
Computed Properties
- Exact Mass: 328.16752
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 24
- Rotatable Bond Count: 6
Experimental Properties
- Density: 1.152±0.06 g/cm3 (20 oC 760 Torr),
- Solubility: Almost insoluble (0.015 g/l) (25 o C),
- PSA: 66.76
Sobetirome Security Information
- Hazardous Material transportation number:NONH for all modes of transport
- Storage Condition:Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
Sobetirome Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci10048-10mg |
Sobetirome |
211110-63-3 | 98% | 10mg |
¥1423.00 | 2023-09-09 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci10048-50mg |
Sobetirome |
211110-63-3 | 98% | 50mg |
¥5704.00 | 2023-09-09 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-1 mg |
Sobetirome |
211110-63-3 | 98.25% | 1mg |
¥399.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-5 mg |
Sobetirome |
211110-63-3 | 98.25% | 5mg |
¥958.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-10 mg |
Sobetirome |
211110-63-3 | 98.25% | 10mg |
¥1448.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-25 mg |
Sobetirome |
211110-63-3 | 98.25% | 25mg |
¥3159.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-50 mg |
Sobetirome |
211110-63-3 | 98.25% | 50mg |
¥5898.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | T5313-1 mL * 10 mM (in DMSO) |
Sobetirome |
211110-63-3 | 98.25% | 1 mL * 10 mM (in DMSO) |
¥1056.00 | 2022-02-28 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | S61650-50mg |
Sobetirome |
211110-63-3 | 50mg |
¥10722.0 | 2021-09-07 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | S61650-5mg |
Sobetirome |
211110-63-3 | 5mg |
¥1782.0 | 2021-09-07 |
Sobetirome Related Literature
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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2. An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3nanoparticlesAdrian Brandt,Florian Winter,Sebastian Klamor,Frank Berkemeier,Jatinkumar Rana,Rainer P?ttgen,Andrea Balducci J. Mater. Chem. A, 2013,1, 11229-11236
-
Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
-
Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
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Marta Liras,Isabel Quijada-Garrido,Marta Palacios-Cuesta,Sonia Mu?oz-Durieux,Olga García Polym. Chem., 2014,5, 433-442
Additional information on Sobetirome
Sobetirome: A Comprehensive Overview
Sobetirome, also known by its CAS number 211110-63-3, is a compound that has garnered significant attention in the field of pharmacology and medical research. This compound is primarily recognized for its potential therapeutic applications in various medical conditions, particularly those related to metabolic disorders and cardiovascular health. Recent studies have shed light on its unique mechanisms of action and its potential to address unmet medical needs.
Sobetirome is a synthetic derivative of a naturally occurring metabolite, which has been extensively studied for its ability to modulate key pathways involved in lipid metabolism and energy homeostasis. The compound's structure has been optimized to enhance its bioavailability and efficacy, making it a promising candidate for therapeutic interventions. Researchers have demonstrated that Sobetirome exhibits potent effects on reducing low-density lipoprotein (LDL) cholesterol levels, which is a critical factor in the prevention of cardiovascular diseases.
The development of Sobetirome was driven by the need for novel agents that can effectively manage dyslipidemia, a condition characterized by abnormal levels of lipids in the blood. Traditional therapies, such as statins, have been the mainstay of treatment; however, they are not suitable for all patients due to side effects or limited efficacy. Sobetirome, on the other hand, offers a different mechanism of action by targeting the liver's ability to produce cholesterol. This approach has shown promise in clinical trials, where it demonstrated significant reductions in LDL cholesterol levels without major adverse effects.
Recent advancements in the understanding of Sobetirome's pharmacokinetics have further enhanced its potential as a therapeutic agent. Studies have shown that the compound is well-absorbed orally and has a favorable safety profile, with minimal off-target effects. These findings are particularly encouraging for patients who are unable to tolerate conventional lipid-lowering medications.
One of the most exciting aspects of Sobetirome research is its potential application beyond dyslipidemia. Preclinical studies suggest that it may also play a role in managing other metabolic disorders, such as obesity and type 2 diabetes. By modulating pathways involved in energy expenditure and glucose metabolism, Sobetirome could offer a multifaceted approach to addressing these conditions.
The clinical development of Sobetirome has been rapid, with several phase II and III trials completed or underway. These trials have provided robust evidence supporting its efficacy and safety profile. Regulatory agencies have expressed interest in advancing this compound towards approval, which could pave the way for its widespread use in clinical practice.
In conclusion, Sobetirome (CAS No. 211110-63-3) represents a significant advancement in the field of lipid metabolism and metabolic disease management. With its unique mechanism of action, favorable safety profile, and potential for treating multiple conditions, it holds great promise for improving patient outcomes. As research continues to unfold, Sobetirome may become an essential tool in the fight against cardiovascular diseases and other metabolic disorders.
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