structure of 4-[(2-aminoethyl)sulfamoyl]-1-methyl-1h-pyrrole-2-carboxamide

4-[(2-aminoethyl)sulfamoyl]-1-methyl-1h-pyrrole-2-carboxamide

CAS No.: 1000932-88-6
M. Wt: 246.29
M. Fa: C8H14N4O3S
InChI Key: BZDHQNOBMSRBAH-UHFFFAOYSA-N

Names and Identifiers of 1000932-88-6

CAS Number

1000932-88-6

MDL Number

MFCD09971413

IUPAC Name

4-[(2-aminoethyl)sulfamoyl]-1-methyl-1H-pyrrole-2-carboxamide

InChI

InChI=1S/C8H14N4O3S/c1-12-5-6(4-7(12)8(10)13)16(14,15)11-3-2-9/h4-5,11H,2-3,9H2,1H3,(H2,10,13)

InChIKey

BZDHQNOBMSRBAH-UHFFFAOYSA-N

Canonical SMILES

CN1C=C(S(=O)(=O)NCCN)C=C1C(N)=O

UNSPSC Code

12352100

Physical and chemical properties of 1000932-88-6

H Bond Acceptors

4

H Bond Donors

3

LogP

-2.34251443765241

Molecular Formula

C8H14N4O3S

Molecular Weight

246.29

Safety Information of 1000932-88-6

Pictograms

Signal Word

 Warning

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

Applications of 1000932-88-6

The applications of 4-[(2-aminoethyl)sulfamoyl]-1-methyl-1H-pyrrole-2-carboxamide are primarily in medicinal chemistry and pharmaceutical development. Potential applications include:

  • Antibacterial Agents: Leveraging its sulfonamide structure for developing new antibiotics.
  • Anti-inflammatory Drugs: Investigating its effects on inflammatory pathways.
  • Research Tools: As a biochemical probe in studies related to enzyme inhibition or receptor binding.

Interaction Studies of 1000932-88-6

Interaction studies involving this compound focus on its binding affinity to various biological targets, including enzymes involved in metabolic pathways and receptors related to inflammation and infection. Understanding these interactions is crucial for elucidating its mechanism of action and optimizing its therapeutic profile.

Biological Activity of 1000932-88-6

4-[(2-aminoethyl)sulfamoyl]-1-methyl-1H-pyrrole-2-carboxamide exhibits promising biological activities, particularly due to its sulfonamide component. Sulfonamides are known for their antibacterial effects by inhibiting bacterial folic acid synthesis. Additionally, this compound may exhibit anti-inflammatory properties and could be explored for potential applications in treating conditions such as ulcers or other inflammatory diseases.