CAS 102649-78-5

N-(6-phenylhexyl)-5-chloro-1-*naphthalenesulfonam

Description:

N-(6-phenylhexyl)-5-chloro-1-naphthalenesulfonamide, identified by its CAS number 102649-78-5, is a chemical compound that features a naphthalene ring system substituted with a sulfonamide group and a phenylhexyl side chain. This compound exhibits characteristics typical of sulfonamides, including potential antibacterial properties, although its specific biological activity may vary. The presence of the chlorine atom at the 5-position of the naphthalene ring can influence its reactivity and solubility. The phenylhexyl group contributes to the compound's hydrophobic nature, which may affect its interaction with biological membranes and its overall pharmacokinetics. Additionally, the structural complexity of this compound suggests potential applications in medicinal chemistry, particularly in the development of new therapeutic agents. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its stability and reactivity would be influenced by the electronic and steric effects of the substituents present.

Formula: C₂₂H₂₄ClNO₂S

InChI: InChI=1/C22H24ClNO2S/c23-21-15-8-14-20-19(21)13-9-16-22(20)27(25,26)24-17-7-2-1-4-10-18-11-5-3-6-12-18/h3,5-6,8-9,11-16,24H,1-2,4,7,10,17H2

SMILES: C(CCCNS(=O)(=O)c1cccc2c1cccc2Cl)CCc1ccccc1

Synonyms:

• N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide
• 6-Phcns
• Sc-9
• 1-Naphthalenesulfonamide, 5-chloro-N-(6-phenylhexyl)-
• 5-chloro-N-(6-phenylhexyl)naphthalene-1-sulfonamide

SC-9

CAS: 102649-78-5

Formula: C₂₂H₂₄ClNO₂S

Color and Shape: Solid

Molecular weight: 401.9495

Ref: IN-DA00080G

N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide

CAS: 102649-78-5

Formula: C₂₂H₂₄ClNO₂S

Molecular weight: 401.95

Ref: 7W-GK4489

N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide

Controlled Product

CAS: 102649-78-5

Applications Activates protein kinase C in a Ca2+-dependent manner, via a mechanism similar to that of phosphatidylserine.
References Nishino, H., et al.: Biochim. Biophys. Acta, 889, 236 (1986), Blest, A.D., et al.: J. Comp. Physiol., 170, 189 (1992), Yau, W.M., et al.: Am. J. Physiol., 263, G659 (1992)

Formula: C₂₂H₂₄ClNO₂S

Color and Shape: Light Yellow

Molecular weight: 401.95

Ref: TR-P330000

N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide

CAS: 102649-78-5

N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide is a dibutyryl camp analog that has been shown to inhibit the L-type calcium channel in a dose-dependent manner. It has an effect on both spermatozoa and glioma cells, with its most significant effect being inhibition of the intracellular calcium ion. This drug inhibits the growth rate of these cells, which may be due to its ability to activate adrenergic receptors and cause increased intracellular calcium ion levels. N-(6-Phenylhexyl)-5-chloro-1-naphthalenesulfonamide also slows the cycle of the cell, which may be due to a kinetic effect.

Formula: C₂₂H₂₄ClNO₂S

Purity: Min. 95%

Molecular weight: 401.95 g/mol

Ref: 3D-FP26980

SC-9

CAS: 102649-78-5

SC-9 is a protein kinase C activator.

Formula: C₂₂H₂₄ClNO₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 401.95

Ref: TM-T23334