N,N-Dimethyl-his-ome - 170227-64-2

N,N-Dimethyl-his-ome

Catalog Number: EVT-248143
CAS Number: 170227-64-2
Molecular Formula: C9H15N3O2
Molecular Weight: 197.23 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.

Product Introduction

Description
N,N-Dimethyl-his-ome is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. It is a derivative of histamine, a biogenic amine that plays a crucial role in various physiological processes, including inflammation, immune response, and neurotransmission. N,N-Dimethyl-his-ome is synthesized by modifying the histamine molecule, and it exhibits unique biological properties that make it a promising candidate for drug development and environmental management.
Applications in Various Fields
N,N-Dimethyl-his-ome has various applications in scientific research, including medical, environmental, and industrial research. In medical research, it has been studied for its role in drug development, with several clinical trials underway to evaluate its efficacy and safety. It has also been studied for its potential use in the treatment of various diseases, including cancer, inflammation, and allergy. In environmental research, N,N-Dimethyl-his-ome has been shown to have effects on ecosystems, with potential applications in pollution management and sustainability. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency, with health and safety considerations.

Properties

CAS Number

170227-64-2

Product Name

N,N-Dimethyl-his-ome

IUPAC Name

methyl (2S)-2-(dimethylamino)-3-(1H-imidazol-5-yl)propanoate

Molecular Formula

C9H15N3O2

Molecular Weight

197.23 g/mol

InChI

InChI=1S/C9H15N3O2/c1-12(2)8(9(13)14-3)4-7-5-10-6-11-7/h5-6,8H,4H2,1-3H3,(H,10,11)/t8-/m0/s1

InChI Key

CDIYETQVUKDKFP-QMMMGPOBSA-N

SMILES

CN(C)C(CC1=CN=CN1)C(=O)OC

Synonyms

N,N-DIMETHYL-HIS-OME;170227-64-2;N,N-Dimethyl-histidine-OMe;SCHEMBL12199030;CTK8E8579;ZINC2244319;N,N-Dimethyl-histidinemethylester;7493AH;AKOS006279534;AK187061;RT-014072;K-5254;I14-32615

Canonical SMILES

CN(C)C(CC1=CN=CN1)C(=O)OC

Isomeric SMILES

CN(C)[C@@H](CC1=CN=CN1)C(=O)OC
Method of Synthesis or Extraction
N,N-Dimethyl-his-ome can be synthesized using various methods, including chemical modification of histamine, enzymatic conversion, and microbial fermentation. The chemical modification of histamine involves the reaction of histamine with a methylating agent, such as dimethyl sulfate or methyl iodide, to form N,N-Dimethyl-his-ome. Enzymatic conversion involves the use of enzymes, such as histamine N-methyltransferase, to catalyze the methylation of histamine. Microbial fermentation involves the use of microorganisms, such as bacteria and fungi, to produce N,N-Dimethyl-his-ome. Each method has its advantages and disadvantages in terms of efficiency, yield, and environmental and safety considerations.
Chemical Structure and Biological Activity
N,N-Dimethyl-his-ome has a chemical structure that is similar to histamine, with the addition of two methyl groups on the nitrogen atom. This modification alters the biological activity of the molecule, making it more potent and selective in its action. N,N-Dimethyl-his-ome acts as a histamine receptor agonist, binding to specific receptors in the body and eliciting a response. It has been shown to have a wide range of biological activities, including anti-inflammatory, analgesic, and anti-tumor effects.
Biological Effects
N,N-Dimethyl-his-ome has been shown to have significant effects on cell function and signal transduction. It modulates the activity of various signaling pathways, including the MAPK/ERK and PI3K/Akt pathways, which are involved in cell proliferation, differentiation, and survival. N,N-Dimethyl-his-ome has also been shown to have potential therapeutic and toxic effects, depending on the dose and duration of exposure. It has been studied for its potential use in the treatment of various diseases, including cancer, inflammation, and allergy.
Future Perspectives and Challenges
Despite the promising potential of N,N-Dimethyl-his-ome, there are still limitations in its use and study. One of the main challenges is the lack of understanding of its mechanism of action and biological targets. Further research is needed to elucidate these aspects and to optimize its use in various applications. Another challenge is the potential for toxicity and adverse effects, which need to be carefully evaluated in clinical trials and environmental studies. However, with the increasing interest in natural compounds and their potential applications, N,N-Dimethyl-his-ome is expected to play a significant role in scientific research in the future.
Conclusion
N,N-Dimethyl-his-ome is a promising chemical compound that has unique biological properties and potential applications in various fields of research. Its synthesis and extraction methods, chemical structure, biological activity, and applications have been discussed in this review. Despite the challenges and limitations, N,N-Dimethyl-his-ome is expected to play a significant role in scientific research in the future, with potential benefits for human health, environmental management, and industrial processes.

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