CAS 78957-84-3
:N-(4-aminobutyl)-5-chloro-1-*naphthalenesulfonami
Description:
N-(4-Aminobutyl)-5-chloro-1-naphthalenesulfonamide, identified by its CAS number 78957-84-3, is a chemical compound that features a naphthalene ring substituted with a sulfonamide group and an aminoalkyl chain. This compound typically exhibits characteristics common to sulfonamides, such as potential antibacterial activity, due to the presence of the sulfonamide functional group. The chlorine atom on the naphthalene ring can influence its reactivity and solubility, while the amino group contributes to its ability to form hydrogen bonds, enhancing its interaction with biological targets. The structure suggests that it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, the presence of both hydrophobic (naphthalene) and hydrophilic (sulfonamide and amino) components may affect its pharmacokinetic properties, such as absorption and distribution in biological systems. As with many chemical substances, safety and handling precautions are essential due to potential toxicity or environmental impact.
Formula:C14H18Cl2N2O2S
InChI:InChI=1/C14H17ClN2O2S.ClH/c15-13-7-3-6-12-11(13)5-4-8-14(12)20(18,19)17-10-2-1-9-16;/h3-8,17H,1-2,9-10,16H2;1H
SMILES:C(CCNS(=O)(=O)c1cccc2c1cccc2Cl)CN.Cl
Synonyms:- 4-{[(5-Chloronaphthalen-1-Yl)Sulfonyl]Amino}Butan-1-Aminium Chloride
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Found 3 products.
N-(4-Aminobutyl)-5-chloro-1-naphthalenesulphonamide hydrochloride
CAS:N-(4-Aminobutyl)-5-chloro-1-naphthalenesulphonamide hydrochloridePurity:≥95%N-(4-Aminobutyl)-5-chloro-1-naphthalenesulfonamide Hydrochloride
CAS:Controlled Product<p>Applications N-(4-Aminobutyl)-5-chloro-1-naphthalenesulfonamide is a naphthalenesulfonamide derivative as neoplasm inhibitor.<br></p>Formula:C14H17ClN2O2S·ClHColor and Shape:NeatMolecular weight:349.28Calmodulin antagonist-1
CAS:Calmodulin antagonist-1 (W-7) is a calmodulin (CaM) antagonist that effectively inhibits calmodulin-activated Ca 2+ -phosphodiesterase (PDE) with an IC 50 of 28 μM. This compound also competitively inhibits trypsin-treated Ca 2+ -PDE with respect to cyclic GMP, exhibiting an IC 50 of 375 μM and a K i value of 300 μM.Formula:C14H18Cl2N2O2SColor and Shape:SolidMolecular weight:349.27


