CAS 2437-17-4: 6-hydroxynaphthalene-1-carboxylic acid
Formula:C11H8O3
InChI:InChI=1S/C11H8O3/c12-8-4-5-9-7(6-8)2-1-3-10(9)11(13)14/h1-6,12H,(H,13,14)
InChI key:InChIKey=JCJUKCIXTRWAQY-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C2=C(C=C(O)C=C2)C=CC1
Synonyms:- 1-Naphthalenecarboxylic Acid, 6-Hydroxy-
- 1-Naphthoic acid, 6-hydroxy-
- 2-Hydroxy-5-naphthoic acid
- 6-Hydroxy-1-naphthalenecarboxylic acid
- 6-Hydroxy-1-naphthoic acid
- Hydroxynaphthoicacid 95%
- 6-hydroxynaphthalene-1-carboxylic acid
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Found 5 products.
6-Hydroxy-1-naphthoic acid
CAS:6-Hydroxy-1-naphthoic acidFormula:C11H8O3Purity:98+%Color and Shape: pale brown solidMolecular weight:188.18g/mol6-Hydroxy-1-naphthoic acid
CAS:Formula:C11H8O3Purity:98%Color and Shape:SolidMolecular weight:188.17946-Hydroxy-1-naphthoic Acid
CAS:Formula:C11H8O3Purity:>98.0%(GC)(T)Color and Shape:White to Brown powder to crystalMolecular weight:188.186-Hydroxy-1-naphthoic acid
CAS:6-Hydroxy-1-naphthoic acid is a synthetic carboxylate compound with an analog structure that has been shown to be cytotoxic to cancer cells. It inhibits the activity of protein kinases by binding to ATP, which blocks the phosphorylation of tyrosine residues on proteins. 6-Hydroxy-1-naphthoic acid has been shown to inhibit growth factor receptors and induce apoptosis in tumor cells. The mechanism of action for this drug is believed to be through ring opening and hydrolysis of the naphthalene ring, followed by reaction with p-hydroxybenzoic acid. This results in inhibition of histone deacetylase activity, leading to decreased expression of genes involved in cell proliferation.Formula:C11H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:188.18 g/mol
