CAS 17127-48-9
:Glaziovine
Description:
Glaziovine, with the CAS number 17127-48-9, is a chemical compound that belongs to the class of alkaloids, which are naturally occurring organic compounds that mostly contain basic nitrogen atoms. It is primarily derived from certain plant sources and is known for its potential biological activities. Glaziovine exhibits characteristics typical of alkaloids, including a complex structure that may contribute to its pharmacological properties. The compound has been studied for its effects on various biological systems, although detailed information on its specific applications or mechanisms of action may be limited. As with many alkaloids, Glaziovine may possess both beneficial and toxic effects, depending on the dosage and context of use. Its solubility, stability, and reactivity can vary, influencing its behavior in different environments. Further research is often necessary to fully understand its properties and potential uses in fields such as medicine or agriculture.
Formula:C18H19NO3
InChI:InChI=1/C18H19NO3/c1-19-8-5-11-9-14(22-2)17(21)16-15(11)13(19)10-18(16)6-3-12(20)4-7-18/h3-4,6-7,9,13,21H,5,8,10H2,1-2H3
SMILES:CN1CCc2cc(c(c3c2C1CC13C=CC(=O)C=C1)O)OC
Synonyms:- Glaziovine [INN]
- Ai3-34588
- Glaziovina [INN-Spanish]
- Glaziovinum
- Glaziovinum [INN-Latin]
- Nsc 146052
- Unii-Ke7J8A65P6
- Spiro(2,5-cyclohexadiene-1,7'(1'H)-cyclopent(ij)isoquinolin)-4-one, 2',3',8',8'a-tetrahydro-6'-hydroxy-5'-methoxy-1'-methyl-, (+-)- (9CI)
- 6'-hydroxy-5'-methoxy-1'-methyl-2',3',8',8a'-tetrahydro-1'H,4H-spiro[cyclohexa-2,5-diene-1,7'-cyclopenta[ij]isoquinolin]-4-one
- (+-)-Glaziovine
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Found 2 products.
Glaziovine
CAS:<p>Glaziovine is an agent of anti-ulcerogenic natural alkaloid.</p>Formula:C18H19NO3Purity:98%Color and Shape:SolidMolecular weight:297.35Glaziovine
CAS:Controlled Product<p>Glaziovine is a sesquiterpene lactone that is found in Chinese medicinal herbs. This molecule has been shown to have anxiolytic properties and to be a blood pressure-lowering agent. Glaziovine binds to the benzodiazepine site on the GABA receptor. It exhibits competitive antagonism with respect to GABA, which leads to increased neuronal activity in the central nervous system. The pharmacological profile of glaziovine has been explored using tetrazolium dye and found that it had no effect on mice at doses up to 20 mg/kg, but did show an increase in locomotor activity at higher doses. Glaziovine is structurally related to other molecules such as borohydride reduction and metal hydroxides.</p>Formula:C18H19NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:297.35 g/mol

