Cas no 1116-22-9 (γ-L-Glutamyl L-Glutamic Acid)
γ-L-Glutamyl L-Glutamic Acid Chemical and Physical Properties
Names and Identifiers
-
- (S)-2-((S)-4-Amino-4-carboxybutanamido)pentanedioic acid
- GAMMA-L-GLUTAMYL-L-GLUTAMIC ACID
- H-gamma-Glu-Glu-OH
- H-Glu(Glu-OH)-OH
- H-γ-Glu-Glu-OH
- L-Glutamic acid, L-g-glutamyl-
- g-Glutamylglutamic acid.
- H-g-Glu-Glu-OH
- L-GLUTAMYL-L-GLUTAMIC ACID
- L-Y-GLUTAMYL-L-GLUTAMIC ACID
- γ-Glu-Glu
- γ-L-Glutamyl L-Glutamic Acid
-
- MDL: MFCD00002630
- Inchi: 1S/C10H16N2O7/c11-5(9(16)17)1-3-7(13)12-6(10(18)19)2-4-8(14)15/h5-6H,1-4,11H2,(H,12,13)(H,14,15)(H,16,17)(H,18,19)/t5-,6-/m0/s1
- InChI Key: OWQDWQKWSLFFFR-WDSKDSINSA-N
- SMILES: O=C(CC[C@@H](C(=O)O)N)N[C@H](C(=O)O)CCC(=O)O
Computed Properties
- Exact Mass: 276.09600
- Monoisotopic Mass: 276.095751
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 5
- Hydrogen Bond Acceptor Count: 9
- Heavy Atom Count: 19
- Rotatable Bond Count: 10
- Complexity: 352
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: -2
- Tautomer Count: 2
- XLogP3: -2.3
- Topological Polar Surface Area: 177
Experimental Properties
- Color/Form: Not determined
- Density: 1.3652 (rough estimate)
- Melting Point: 179-182 °C
- Boiling Point: 419.15°C (rough estimate)
- Flash Point: 355.4°C
- Refractive Index: 1.4550 (estimate)
- PSA: 167.02000
- LogP: -0.29610
- Solubility: Not determined
γ-L-Glutamyl L-Glutamic Acid Security Information
- Safety Instruction: S24/25
- Storage Condition:-15°C
γ-L-Glutamyl L-Glutamic Acid Customs Data
- HS CODE:2924199090
- Customs Data:
China Customs Code:
2924199090Overview:
2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
γ-L-Glutamyl L-Glutamic Acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM276367-1g |
(S)-2-((S)-4-Amino-4-carboxybutanamido)pentanedioic acid |
1116-22-9 | 95% | 1g |
$729 | 2021-06-09 | |
| TRC | G245125-10mg |
γ-L-Glutamyl L-Glutamic Acid |
1116-22-9 | 10mg |
$ 63.00 | 2023-09-07 | ||
| TRC | G245125-50mg |
γ-L-Glutamyl L-Glutamic Acid |
1116-22-9 | 50mg |
$ 218.00 | 2023-09-07 | ||
| TRC | G245125-100mg |
γ-L-Glutamyl L-Glutamic Acid |
1116-22-9 | 100mg |
$ 328.00 | 2023-09-07 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | L849301-50mg |
gamma-L-Glutamyl-L-glutamic acid |
1116-22-9 | 98% | 50mg |
¥736.00 | 2022-01-13 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | L849301-250mg |
gamma-L-Glutamyl-L-glutamic acid |
1116-22-9 | 98% | 250mg |
¥2,899.00 | 2022-01-13 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | G36210-50mg |
(S)-2-((S)-4-Amino-4-carboxybutanamido)pentanedioic acid |
1116-22-9 | 98% | 50mg |
¥588.0 | 2023-09-07 | |
| abcr | AB476615-250 mg |
H-Glu(Glu-OH)-OH; . |
1116-22-9 | 250MG |
€257.50 | 2023-07-18 | ||
| abcr | AB476615-1 g |
H-Glu(Glu-OH)-OH; . |
1116-22-9 | 1g |
€674.00 | 2023-07-18 | ||
| eNovation Chemicals LLC | Y1054247-50mg |
H-GAMMA-GLU-GLU-OH |
1116-22-9 | 98% | 50mg |
$170 | 2024-06-07 |
γ-L-Glutamyl L-Glutamic Acid Related Literature
-
Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
-
Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
Additional information on γ-L-Glutamyl L-Glutamic Acid
γ-L-Glutamyl L-Glutamic Acid (CAS No. 1116-22-9): A Comprehensive Overview
γ-L-Glutamyl L-Glutamic Acid, chemically designated as γ-L-glutamyl-L-glutamic acid, is a significant compound in the field of biochemistry and pharmaceutical research. With a CAS number 1116-22-9, this dipeptide has garnered considerable attention due to its multifaceted roles in biological systems and potential applications in drug development. This article provides an in-depth exploration of the compound's chemical properties, biological significance, and the latest research findings that underscore its importance.
The molecular structure of γ-L-Glutamyl L-Glutamic Acid consists of two glutamic acid residues linked by a γ-peptide bond. This configuration imparts unique biochemical properties to the compound, making it a valuable tool in various scientific investigations. The presence of two glutamic acid units enhances its reactivity and solubility, which are critical factors in biochemical assays and pharmaceutical formulations.
One of the most notable applications of γ-L-Glutamyl L-Glutamic Acid is its role as a precursor in the synthesis of glutathione, a crucial antioxidant in human physiology. Glutathione plays a pivotal role in detoxification processes, protecting cells from oxidative damage caused by free radicals. Recent studies have highlighted the potential of γ-L-Glutamyl L-Glutamic Acid as an intermediate in enhancing glutathione levels, thereby bolstering the body's defense mechanisms against oxidative stress.
In addition to its antioxidant properties, γ-L-Glutamyl L-Glutamic Acid has been investigated for its role in neurotransmitter systems. Glutamate is the primary excitatory neurotransmitter in the brain, and its derivatives, including γ-L-Glutamyl L-Glutamic Acid, are being explored for their potential in modulating neural activity. Research indicates that this compound may influence synaptic plasticity and cognitive functions, making it a promising candidate for therapeutic interventions in neurodegenerative disorders.
The pharmaceutical industry has also shown interest in γ-L-Glutamyl L-Glutamic Acid for its potential applications in peptide drug development. Its stable structure and high reactivity make it an ideal candidate for synthesizing complex peptides with therapeutic benefits. For instance, studies have demonstrated its utility in creating novel peptidomimetics that target specific biological pathways. These advancements highlight the compound's versatility and its potential to contribute to the development of next-generation pharmaceuticals.
Recent advancements in synthetic biology have further expanded the applications of γ-L-Glutamyl L-Glutamic Acid. Researchers have developed microbial fermentation processes that efficiently produce this compound on an industrial scale. This innovation has not only improved the availability of γ-L-Glutamyl L-Glutamic Acid but also reduced production costs, making it more accessible for research and commercial applications. Such developments underscore the growing importance of this compound in both academic and industrial settings.
The compound's role in cell signaling pathways has also been a subject of intense research. Studies have revealed that γ-L-Glutamyl L-Glutamic Acid can modulate various intracellular signaling cascades, influencing processes such as inflammation and apoptosis. These findings have opened new avenues for developing therapeutic strategies targeting chronic inflammatory diseases and cancer. The ability of γ-L-Glutamyl L-Glutamic Acid to interact with multiple signaling pathways makes it a multifunctional tool in pharmacological research.
Another area where γ-L-Glutamyl L-Glutamic Acid has shown promise is in nutraceutical applications. Its ability to enhance glutathione synthesis has led to its inclusion in dietary supplements aimed at boosting immune function and reducing oxidative stress. These supplements are particularly popular among individuals seeking to improve their overall health and well-being. The growing demand for such products underscores the commercial viability of γ-L-Glutamyl L-Glutamic Acid-based formulations.
In conclusion, γ-L-Glutamyl L-Glu-tamic Acid (CAS No. 1116-22-9) is a versatile compound with significant implications in biochemistry, pharmacology, and nutraceuticals. Its multifaceted roles as a precursor for glutathione synthesis, a modulator of neurotransmitter systems, and an intermediate in peptide drug development make it a valuable asset in scientific research and therapeutic applications. The recent advancements in synthetic biology and industrial production further enhance its accessibility and potential impact on various fields.
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