Cas no 57-64-7 (Physostigmine Salicylate)
Physostigmine Salicylate Chemical and Physical Properties
Names and Identifiers
-
- Physostigmine Salicylate
- Eserine salicylate
- [(3aR,8bS)-3,4,8b-trimethyl-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-yl] N-methylcarbamate,2-hydroxybenzoic acid
- ESERINE SALICYLATE SALT
- ESERINE SALICYLATE(RG)
- PHYSOSTIGMINE SALICYLATE (1:1)
-
- MDL: MFCD00135659
- Inchi: 1S/C15H21N3O2.C7H6O3/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2;8-6-4-2-1-3-5(6)7(9)10/h5-6,9,13H,7-8H2,1-4H3,(H,16,19);1-4,8H,(H,9,10)/t13-,15+;/m1./s1
- InChI Key: HZOTZTANVBDFOF-PBCQUBLHSA-N
- SMILES: O(C(NC)=O)C1C=CC2=C(C=1)[C@]1(C)CCN(C)[C@@H]1N2C.OC1C=CC=CC=1C(=O)O
Computed Properties
- Exact Mass: 413.19500
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 30
- Rotatable Bond Count: 3
- Complexity: 535
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 8
- XLogP3: nothing
Experimental Properties
- Melting Point: 181-183?°C
- PSA: 102.34000
- LogP: 3.25810
- Merck: 7384
Physostigmine Salicylate Security Information
- Hazardous Material transportation number:UN 1544 6.1/PG 1
- WGK Germany:3
- Hazard Category Code: 26/28
- Safety Instruction: S25-S45
- RTECS:TJ2450000
-
Hazardous Material Identification:
- HazardClass:6.1(a)
- PackingGroup:II
- Toxicity:LD50 i.p. in mice: 0.64 mg/kg (Sofia, Knabloch)
- Packing Group:II
- Hazard Level:6.1(a)
- Safety Term:6.1(a)
- Packing Group:II
- Risk Phrases:R26/28
Physostigmine Salicylate Customs Data
- HS CODE:2933990090
- Customs Data:
China Customs Code:
2933990090Overview:
2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Physostigmine Salicylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| MedChemExpress | HY-B1266-5mg |
Physostigmine salicylate |
57-64-7 | 99.74% | 5mg |
¥1124 | 2025-04-16 | |
| MedChemExpress | HY-B1266-10mg |
Physostigmine salicylate |
57-64-7 | 99.74% | 10mg |
¥1900 | 2025-04-16 | |
| MedChemExpress | HY-B1266-25mg |
Physostigmine salicylate |
57-64-7 | 99.74% | 25mg |
¥3688 | 2025-04-16 | |
| MedChemExpress | HY-B1266-50mg |
Physostigmine salicylate |
57-64-7 | 99.74% | 50mg |
¥5675 | 2025-04-16 | |
| MedChemExpress | HY-B1266-100mg |
Physostigmine salicylate |
57-64-7 | 99.37% | 100mg |
¥3000 | 2023-08-31 | |
| ChemScence | CS-0013051-5mg |
Physostigmine (salicylate) |
57-64-7 | ≥99.00% | 5mg |
$50.0 | 2022-04-27 | |
| ChemScence | CS-0013051-10mg |
Physostigmine (salicylate) |
57-64-7 | ≥99.00% | 10mg |
$80.0 | 2022-04-27 | |
| ChemScence | CS-0013051-25mg |
Physostigmine (salicylate) |
57-64-7 | ≥99.00% | 25mg |
$140.0 | 2022-04-27 | |
| ChemScence | CS-0013051-50mg |
Physostigmine (salicylate) |
57-64-7 | ≥99.00% | 50mg |
$210.0 | 2022-04-27 | |
| ChemScence | CS-0013051-100mg |
Physostigmine (salicylate) |
57-64-7 | ≥99.00% | 100mg |
$300.0 | 2022-04-27 |
Physostigmine Salicylate Suppliers
Physostigmine Salicylate Related Literature
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Xiaofeng Lin RSC Adv., 2016,6, 9002-9006
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Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
Additional information on Physostigmine Salicylate
Physostigmine Salicylate and CAS No. 57-64-7: A Comprehensive Overview
Physostigmine Salicylate, a derivative of the naturally occurring alkaloid physostigmine, is a compound of significant interest in the field of pharmacology and medicinal chemistry. With the CAS number CAS No. 57-64-7, this compound has been extensively studied for its potential therapeutic applications. The molecular structure of Physostigmine Salicylate incorporates both the physostigmine moiety and a salicylate group, which synergistically enhance its pharmacological properties. This introduction delves into the chemical properties, pharmacological effects, and recent research advancements associated with Physostigmine Salicylate.
The chemical structure of Physostigmine Salicylate can be described as a chiral compound with a tertiary amine group, which is crucial for its interaction with cholinergic receptors. The salicylate moiety contributes to its solubility and stability, making it a suitable candidate for pharmaceutical formulations. The compound's ability to cross the blood-brain barrier has made it particularly valuable in the study of central nervous system disorders. Recent studies have highlighted its potential in treating cognitive impairments and neurodegenerative diseases, leveraging its cholinesterase inhibitory activity.
In terms of pharmacological effects, Physostigmine Salicylate exhibits potent acetylcholinesterase inhibition, which leads to an increase in acetylcholine levels in the synaptic cleft. This mechanism is particularly relevant in conditions where cholinergic neurotransmission is compromised, such as Alzheimer's disease and myasthenia gravis. The compound's dual action on both central and peripheral nervous systems makes it a versatile therapeutic agent. Additionally, its salicylate component provides anti-inflammatory properties, further broadening its therapeutic spectrum.
Recent research has explored the potential of Physostigmine Salicylate in neuroprotection and cognitive enhancement. Studies have demonstrated its ability to modulate neurotransmitter systems involved in learning and memory, suggesting its utility in treating cognitive decline associated with aging and neurodegenerative disorders. The compound's ability to enhance cholinergic signaling has also been linked to improvements in attention and executive functions. These findings have prompted further investigation into its role in cognitive rehabilitation therapies.
The synthesis and characterization of Physostigmine Salicylate have been subjects of extensive research. Advanced synthetic methodologies have enabled the production of high-purity forms of the compound, facilitating more accurate pharmacological studies. Techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been instrumental in elucidating its molecular structure and dynamics. These advancements have not only improved our understanding of the compound's pharmacokinetics but also paved the way for novel drug formulations.
The clinical application of Physostigmine Salicylate has been evaluated in various therapeutic settings. Its use as an acetylcholinesterase inhibitor has shown promise in managing symptoms associated with Alzheimer's disease, where cognitive decline is primarily driven by cholinergic deficits. Additionally, the compound has been investigated for its potential role in treating myasthenia gravis, a neuromuscular disorder characterized by muscle weakness and fatigue. Clinical trials have demonstrated its efficacy in improving muscle strength and reducing symptoms.
Future directions in the research of Physostigmine Salicylate include exploring its potential as a prodrug or combination therapy agent. By modifying its chemical structure or combining it with other bioactive compounds, researchers aim to enhance its therapeutic efficacy while minimizing side effects. The development of targeted drug delivery systems has also been a focus area, with the goal of improving bioavailability and reducing systemic toxicity. These innovations hold promise for expanding the clinical applications of Physostigmine Salicylate.
The environmental impact and sustainability considerations of Physostigmine Salicylate production are also gaining attention. Green chemistry principles have been applied to optimize synthetic routes, reducing waste generation and energy consumption. Efforts to develop biodegradable formulations further align with sustainable practices, ensuring minimal environmental footprint throughout the lifecycle of the compound.
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