- (S)-Rasagiline
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- $89.00 / 1mL
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2024-10-24
- CAS:185517-74-2
- Min. Order:
- Purity:
- Supply Ability: 10g
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| (S)-2,3-DIHYDRO-N-METHYL-N-2-PROPYNYL-1H-INDEN-1-AMINE Basic information |
| (S)-2,3-DIHYDRO-N-METHYL-N-2-PROPYNYL-1H-INDEN-1-AMINE Chemical Properties |
Boiling point | 305.5±30.0 °C(Predicted) | density | 1.05±0.1 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | DMSO: ≥15mg/mL | form | powder | pka | 6.95±0.20(Predicted) | color | Light yellow to yellow |
Hazard Codes | Xn,N | Risk Statements | 22-50 | Safety Statements | 61 | RIDADR | UN 3077 9 / PGIII | WGK Germany | 3 | RTECS | NK8216500 | HS Code | 2921490090 |
| (S)-2,3-DIHYDRO-N-METHYL-N-2-PROPYNYL-1H-INDEN-1-AMINE Usage And Synthesis |
Uses | (S)-Rasagiline (TVP1022) is the relatively inactive S-enantiomer form of Rasagiline. Rasagiline is a highly potent selective irreversible MAO inhibitor with IC50s of 4.43 nM and 412 nM for rat brain MAO B and A activity, respectively[1]. (S)-Rasagiline is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | Biological Activity | TVP1022, the S-isomer of rasagiline, an anti-Parkinson drug, appears to have the same neuroprotective activity as the R-isomer, but is 1000-fold less active as an MAO-B inhibitor. TVP1022, a neuroprotective and cytoprotective molecule, is also cardioprotective in r at models. Its activity is believed to involve stabilization of mitochondrial membrane potential, induction of Bcl-2 and activation of the PKC signalling pathway, enhancing the phosphorylation of protein kinase C and glycogen synthase kinase-3β. | References | [1] M B Youdim, et al. Rasagiline [N-propargyl-1R(+)-aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B. Br J Pharmacol. 2001 Jan;132(2):500-6. DOI:10.1038/sj.bjp.0703826 |
| (S)-2,3-DIHYDRO-N-METHYL-N-2-PROPYNYL-1H-INDEN-1-AMINE Preparation Products And Raw materials |
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