Product Name | Tolcapone |
Description |
COMT inhibitor |
Purity | >98% (TLC); NMR (Conforms) |
CAS No. | 134308-13-7 |
Molecular Formula | C14H11NO5 |
Molecular Weight | 273.2 |
Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Storage Temperature | -20ºC |
Shipping Temperature | Shipped Ambient |
Product Type | Inhibitor |
Solubility | Soluble in DMSO (25 mg/ml), or ethanol (25 mg/ml) |
Source | Synthetic |
Appearance | Yellow powder |
SMILES | Cc1ccc(cc1)C(=O)c2cc(O)c(O)c(c2)[N+]([O-])=O |
InChI | 1S/C14H11NO5/c1-8-2-4-9(5-3-8)13(17)10-6-11(15(19)20)14(18)12(16)7-10/h2-7,16,18H,1H3 |
InChIKey | MIQPIUSUKVNLNT-UHFFFAOYSA-N |
Safety Phrases |
Classification: Not WHMIS controlled Hazard statement(s): H303 - May be harmful if swallowed. H400 - Very toxic to aquatic life. Precautionary statement(s) P273 Avoid release to the environment. |
Cite This Product | Tolcapone (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-540) |
Alternative Names | (3,4-dihydroxy-5-nitrophenyl)-(4-methylphenyl)methanone, Tolcapone, Tasmar, Ro 40-7592 |
Research Areas | Neurodegeneration, Neuroscience, Parkinson's Disease |
PubChem ID | 4659569 |
Scientific Background | Tolcapone is a COMT inhibitor. It inhibits both central and peripheral nervous system catechol-O-methyltransferase (COMT). |
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