CAS 3468-01-7: 3-Methylflavone-8-carboxylic acid
Formula:C17H12O4
InChI:InChI=1S/C17H12O4/c1-10-14(18)12-8-5-9-13(17(19)20)16(12)21-15(10)11-6-3-2-4-7-11/h2-9H,1H3,(H,19,20)
InChI key:InChIKey=KMMBBZOSQNLLMN-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C2C(C(=O)C(C)=C(O2)C3=CC=CC=C3)=CC=C1
Synonyms:- 3 Methylflavone-8-carboxylate
- 3-Methyl Flavone-8-Carboxylic Acid
- 3-Methyl-4-oxo-2-phenyl-4H-1-benzopyran-8-carboxylic acid
- 3-Methyl-4-oxo-2-phenylchromene-8-carboxylic acid
- 3-methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid
- 4H-1-Benzopyran-8-carboxylic acid, 3-methyl-4-oxo-2-phenyl-
- 8-Carboxy-3-methylflavone
- Mfca
- 3-Methylflavone-8-carboxylic acid
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Found 11 products.
3-Methylflavone-8-carboxylic Acid
CAS:Formula:C17H12O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:280.283-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid
CAS:Formula:C17H12O4Purity:98%Color and Shape:SolidMolecular weight:280.27483-Methylflavone-8-carboxylic acid
CAS:3-Methylflavone-8-carboxylic acidFormula:C17H12O4Purity:98%Molecular weight:280.27g/molFlavoxate Related Compound A (3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid)
CAS:Aromatic heterocyclic compounds with oxygen hetero-atom(s) only, nesoiFormula:C17H12O4Color and Shape:White Off-White PowderMolecular weight:280.07356Flavoxate EP Impurity A (Flavoxate USP Related Compound A)
CAS:Formula:C17H12O4Color and Shape:White To Off-White SolidMolecular weight:280.283-Methylflavone-8-carboxylic acid
CAS:3-Methylflavone-8-carboxylic acid is a synthetic compound, which is known primarily as an antagonist of the gamma-aminobutyric acid (GABA) receptor system. This product is derived from chemical synthesis processes involving flavone derivatives. The mode of action involves competitive inhibition at the GABA-A receptor sites, thereby modulating neurotransmitter activity within the central nervous system. Primarily used in neuroscientific research, 3-Methylflavone-8-carboxylic acid aids in the exploration of GABAergic signaling pathways and their physiological effects. It provides a tool for studying the modulation of synaptic transmission and neuron excitability, which are crucial for understanding various neurological and psychiatric disorders. By elucidating the mechanistic pathways of GABA antagonism, it offers insights into potential therapeutic targets for conditions such as anxiety, epilepsy, and sleep disorders. The compound's ability to selectively interact with GABA receptors makes it a valuable asset in experimental pharmacology and related fields.Formula:C17H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:280.27 g/mol3-Methylflavone-8-carboxylic acid
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:280.27899169921875
