structure of 1-Sulfamoylpiperidine-4-carboxylic acid

1-Sulfamoylpiperidine-4-carboxylic acid

CAS No.: 1000932-67-1
M. Wt: 208.24
M. Fa: C6H12N2O4S
InChI Key: RHSCFCIWXIKLFP-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 1-Sulfamoylpiperidine-4-carboxylic acid

CAS Number

1000932-67-1

EC Number

850-767-8

MDL Number

MFCD09940510

IUPAC Name

1-sulfamoylpiperidine-4-carboxylic acid

InChI

InChI=1S/C6H12N2O4S/c7-13(11,12)8-3-1-5(2-4-8)6(9)10/h5H,1-4H2,(H,9,10)(H2,7,11,12)

InChIKey

RHSCFCIWXIKLFP-UHFFFAOYSA-N

Canonical SMILES

C1CN(CCC1C(=O)O)S(=O)(=O)N

UNSPSC Code

12352100

Physical and chemical properties of 1-Sulfamoylpiperidine-4-carboxylic acid

Molecular Formula

C6H12N2O4S

Molecular Weight

208.24

Safety Information of 1-Sulfamoylpiperidine-4-carboxylic acid

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1-Sulfamoylpiperidine-4-carboxylic acid

1-Sulfamoylpiperidine-4-carboxylic acid has potential applications in:

  • Pharmaceutical Development: As a lead compound for developing new antibacterial agents or drugs targeting specific biological pathways.
  • Research: Used in studies related to enzyme inhibition and drug design due to its unique structural features.

Interaction Studies of 1-Sulfamoylpiperidine-4-carboxylic acid

Interaction studies involving 1-sulfamoylpiperidine-4-carboxylic acid focus on its binding affinity to various biological targets. These studies typically employ techniques such as:

  • Molecular Docking: To predict how the compound interacts with target proteins.
  • Enzyme Inhibition Assays: To evaluate its effectiveness against specific enzymes, particularly those involved in bacterial metabolism.

Such studies are crucial for understanding the therapeutic potential and mechanism of action of this compound.

Biological Activity of 1-Sulfamoylpiperidine-4-carboxylic acid

The biological activity of 1-sulfamoylpiperidine-4-carboxylic acid is primarily attributed to its structural components. Compounds with sulfamoyl groups are often associated with antibacterial properties due to their ability to inhibit bacterial enzymes such as dihydropteroate synthase. Additionally, the piperidine ring is known to interact with various biological targets, potentially influencing neurotransmitter systems and exhibiting analgesic or anti-inflammatory effects.