Cas no 315-69-5 (Dehydro trimipramine)
Dehydro trimipramine Chemical and Physical Properties
Names and Identifiers
-
- Dehydro trimipramine
- Trimipramine Related Compound A
- 3-benzo[b][1]benzazepin-11-yl-N,N,2-trimethylpropan-1-amine
- 5-<2-Methyl-3-dimethylamino-propyl>-iminostilben
- UNII-4988Q8TXP6
- 5-[3-(Dimethylamino)-2-methylpropyl]-5H-dibenz[b,f]azepine
- N,Nβ-Trimethyl-5H-dibenz[b,f]azepine-5-propanamine
- (2RS)-3-(5H-Dibenzo[b,f]azepin-5-yl)-N,N,2-trimethylpropan-1-amine (Dehydrotrimipramine)
- Q27259254
- Oprea1_338922
- Trimipramine Related Compound A (25 mg) (dehydro trimipramine)
- N,N,ss-Trimethyl-5H-dibenz[b,f]azepine-5-propanamine; 5-[3-(Dimethylamino)-2-methylpropyl]-5H-dibenz[b,f]azepine; Dehydro trimipramine; Trimipramine Related Compound A; Trimipramine Maleate Impurity C; Trimipramine Impurity C
- TRIMIPRAMINE MALEATE IMPURITY C [EP IMPURITY]
- 4988Q8TXP6
- Trimipramine maleate specified impurity C [EP]
- 315-69-5
-
- Inchi: 1S/C20H24N2/c1-16(14-21(2)3)15-22-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)22/h4-13,16H,14-15H2,1-3H3
- InChI Key: RNFADUFBCJRRPS-UHFFFAOYSA-N
- SMILES: N1(C2C=CC=CC=2C=CC2C=CC=CC1=2)CC(C)CN(C)C
Computed Properties
- Exact Mass: 292.19400
- Monoisotopic Mass: 292.193948774g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 22
- Rotatable Bond Count: 4
- Complexity: 350
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.9
- Topological Polar Surface Area: 6.5?2
Experimental Properties
- PSA: 6.48000
- LogP: 4.57120
Dehydro trimipramine Security Information
- Hazardous Material transportation number:NONH for all modes of transport
Dehydro trimipramine Customs Data
- HS CODE:2925290090
- Customs Data:
China Customs Code:
2925290090Overview:
2925290090 Other imines and their derivatives,And their salt.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2925290090 other imines and their derivatives; salts thereof.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%
Dehydro trimipramine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 1692710-25MG |
Trimipramine Related Compound A |
315-69-5 | 25mg |
¥8035.02 | 2025-01-16 | ||
| TRC | D230410-5mg |
Dehydro Trimipramine |
315-69-5 | 5mg |
$ 201.00 | 2023-04-17 | ||
| TRC | D230410-25mg |
Dehydro Trimipramine |
315-69-5 | 25mg |
$ 781.00 | 2023-04-17 | ||
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 1692710-25MG |
315-69-5 | 25MG |
¥16466.89 | 2023-01-05 |
Dehydro trimipramine Related Literature
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Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
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Eunice Y.-L. Hui,Bhimsen Rout,Yaw Sing Tan,Kok-Ping Chan,Charles W. Johannes Org. Biomol. Chem., 2018,16, 389-392
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P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
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S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115
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Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
Additional information on Dehydro trimipramine
Dehydro Trimipramine: A Comprehensive Overview
Dehydro trimipramine, with the CAS number 315-69-5, is a compound of significant interest in the fields of pharmacology and medicinal chemistry. This compound is a derivative of trimipramine, a tricyclic antidepressant, and has been studied for its potential therapeutic applications. The long-term stability and bioavailability of dehydro trimipramine have been extensively investigated, making it a promising candidate for various medical interventions.
The chemical structure of dehydro trimipramine is characterized by a tricyclic framework, which contributes to its unique pharmacokinetic properties. Recent studies have highlighted its ability to modulate serotonin and norepinephrine reuptake, similar to its parent compound, trimipramine. However, dehydro trimipramine exhibits distinct metabolic pathways and pharmacodynamic profiles, which may offer advantages in terms of reduced side effects and improved efficacy.
One of the most notable advancements in the study of dehydro trimipramine is its potential application in the treatment of neurodegenerative diseases. Researchers have explored its role in mitigating oxidative stress and inflammation, two key factors in conditions such as Alzheimer's disease and Parkinson's disease. The compound's ability to cross the blood-brain barrier efficiently has further underscored its potential as a neuroprotective agent.
In addition to its neuroprotective properties, dehydro trimipramine has shown promise in addressing mood disorders and anxiety. Clinical trials have demonstrated that it may provide relief from symptoms associated with these conditions without inducing the same level of sedation or anticholinergic effects commonly seen with traditional tricyclic antidepressants. This makes it an attractive option for patients who require targeted therapies with fewer adverse effects.
The synthesis of dehydro trimipramine involves a series of intricate chemical reactions, including oxidation and cyclization steps. These processes are optimized to ensure high purity and consistency in the final product. The compound's synthetic pathway has been refined over the years, with researchers focusing on improving yield and reducing costs associated with large-scale production.
From an analytical standpoint, dehydro trimipramine is often characterized using advanced techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry. These methods allow for precise quantification and structural elucidation, ensuring that the compound meets rigorous quality control standards. The use of these techniques has also facilitated the identification of metabolites and degradation products, which are critical for understanding its pharmacokinetics.
Recent breakthroughs in computational chemistry have enabled researchers to model the interactions of dehydro trimipramine with various biological targets. Molecular docking studies have provided insights into its binding affinity for serotonin and norepinephrine transporters, as well as other receptors implicated in mental health disorders. These computational approaches have significantly accelerated drug discovery efforts by predicting potential drug candidates with high accuracy.
The regulatory landscape surrounding dehydro trimipramine is another area of active research. As regulatory agencies increasingly emphasize evidence-based medicine, there is a growing need for robust clinical data to support its use in therapeutic settings. Ongoing phase II clinical trials are focusing on establishing its safety profile, efficacy, and optimal dosing regimen across different patient populations.
In conclusion, dehydro trimipramine represents a compelling avenue for advancing therapeutic interventions in mental health and neurodegenerative disorders. Its unique chemical properties, coupled with recent advancements in research methodologies, position it as a potential cornerstone in future treatment regimens. As further studies unfold, the full extent of its therapeutic potential will continue to emerge.
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