CAS 195199-95-2

N,3-Dimethyl-N-[(1R)-1-methyl-3-(4-methyl-1-piperidinyl)propyl]benzenesulfonamide

Description:

N,3-Dimethyl-N-[(1R)-1-methyl-3-(4-methyl-1-piperidinyl)propyl]benzenesulfonamide, with CAS number 195199-95-2, is a chemical compound characterized by its sulfonamide functional group, which is known for its applications in medicinal chemistry. This compound features a complex structure that includes a benzenesulfonamide moiety, which contributes to its potential biological activity. The presence of multiple methyl groups and a piperidine ring suggests that it may exhibit lipophilic properties, enhancing its ability to penetrate biological membranes. The stereochemistry indicated by the (1R) configuration implies specific spatial arrangements that can influence the compound's interaction with biological targets, potentially affecting its pharmacological profile. Such compounds are often investigated for their roles in drug development, particularly in the context of treating various conditions, including neurological disorders. Overall, the unique structural features of this sulfonamide derivative may contribute to its efficacy and specificity in therapeutic applications.

Formula: C₁₈H₃₀N₂O₂S

InChI: InChI=1S/C18H30N2O2S/c1-15-8-11-20(12-9-15)13-10-17(3)19(4)23(21,22)18-7-5-6-16(2)14-18/h5-7,14-15,17H,8-13H2,1-4H3/t17-/m1/s1

InChI key: InChIKey=AGVNHDNTFYHZNL-QGZVFWFLSA-N

SMILES: S(N([C@@H](CCN1CCC(C)CC1)C)C)(=O)(=O)C2=CC(C)=CC=C2

Synonyms:

• Benzenesulfonamide,N,3-dimethyl-N-[1-methyl-3-(4-methyl-1-piperidinyl)propyl]-, (R)-
• N,3-Dimethyl-N-[(1R)-1-methyl-3-(4-methyl-1-piperidinyl)propyl]benzenesulfonamide
• Sb 258719
• Benzenesulfonamide, N,3-dimethyl-N-[(1R)-1-methyl-3-(4-methyl-1-piperidinyl)propyl]-

SB 258719

CAS: 195199-95-2

SB 258719

Purity: ≥98%

Molecular weight: 338.51g/mol

Ref: 54-BUP15322

SB 258719

CAS: 195199-95-2

SB 258719 is a selective 5-HT1A receptor antagonist, which is a type of pharmacological agent that binds to and inhibits the activity of the 5-HT1A receptor. It is synthesized from chemical compounds typically used in neurobiological research. The mode of action involves the competitive blockade of serotonin (5-HT) at the 5-HT1A receptor sites, thereby preventing serotonin from activating these receptors in the brain.

Formula: C₁₈H₃₀N₂O₂S

Purity: Min. 95%

Molecular weight: 338.51 g/mol

Ref: 3D-VHA19995

SB 258719

CAS: 195199-95-2

SB 258719 is a selective antagonist of 5-HT7 receptor with pKi of 7.5.

Formula: C₁₈H₃₀N₂O₂S

Purity: 99.73%

Color and Shape: Solid

Molecular weight: 338.51

Ref: TM-T12855