CAS 1210-84-0
:1H-Indole-3-pentanoic acid
Description:
1H-Indole-3-pentanoic acid, with the CAS number 1210-84-0, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a pentanoic acid side chain at the 3-position of the indole ring, contributing to its unique properties. It is typically a white to off-white solid and is soluble in organic solvents, with limited solubility in water. The presence of the carboxylic acid functional group imparts acidic characteristics, allowing it to participate in various chemical reactions, such as esterification and amidation. 1H-Indole-3-pentanoic acid is of interest in biochemical research, particularly in studies related to plant growth regulators and potential therapeutic applications due to its structural similarity to naturally occurring indole compounds. Its biological activity may include effects on plant hormone signaling pathways, making it relevant in agricultural chemistry. As with many indole derivatives, it may exhibit fluorescence properties, which can be useful in analytical applications.
Formula:C13H15NO2
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Found 2 products.
5-(1H-Indol-3-yl)pentanoic acid
CAS:<p>5-(1H-Indol-3-yl)pentanoic acid is a potent and selective serotonin reuptake inhibitor (SSRI). It has been shown to have a high affinity for the serotonin transporter (SERT), with a binding constant of about 5 nM. The compound has been shown to be bifunctional, which means it can inhibit both serotonin and dopamine reuptake. 5-(1H-Indol-3-yl)pentanoic acid is also orally active, so it can be used in vivo as well as in vitro. This drug has been found to have pharmacokinetic properties that are similar to those of fluoxetine and citalopram. Pharmacophore modeling studies have revealed that this drug binds to the SERT by creating hydrogen bonds with amino acids such as serine, threonine, tyrosine and tryptophan.</p>Formula:C13H15NO2Purity:Min. 95%Molecular weight:217.26 g/mol

