structure of 6-ACETYLAMINO-7-AZAINDOLE

6-ACETYLAMINO-7-AZAINDOLE

CAS No.: 1000341-56-9
M. Wt: 175.187
M. Fa: C9H9N3O
InChI Key: -

Names and Identifiers of 6-ACETYLAMINO-7-AZAINDOLE

CAS Number

1000341-56-9

IUPAC Name

N-(1H-pyrrolo[2,3-b]pyridin-6-yl)ethanamide

Canonical SMILES

CC(=O)NC1=NC2=C(C=C1)C=CN2

Physical and chemical properties of 6-ACETYLAMINO-7-AZAINDOLE

Acidity coefficient

13.48±0.43(Predicted)

Density

1.4±0.1 g/cm3

Exact Mass

175.074554

Index of Refraction

1.725

LogP

1.08

Molecular Formula

C9H9N3O

Molecular Weight

175.187

PSA

61.27000

Storage condition

2-8°C

Applications of 6-ACETYLAMINO-7-AZAINDOLE

N-(1H-Pyrrolo[2,3-b]pyridin-6-yl)acetamide has potential applications in:

  • Pharmaceutical Development: Due to its biological activities, it may serve as a lead compound for developing new drugs targeting cancer or infectious diseases.
  • Chemical Research: This compound can be used as a building block in organic synthesis for creating more complex heterocyclic compounds.

Interaction Studies of 6-ACETYLAMINO-7-AZAINDOLE

Studies on N-(1H-Pyrrolo[2,3-b]pyridin-6-yl)acetamide interactions with biological targets are crucial for understanding its mechanism of action. Key areas of investigation include:

  • Binding Affinity Studies: Determining how well this compound binds to specific enzymes or receptors can provide insights into its therapeutic potential.
  • Mechanistic Studies: Understanding how this compound affects cellular pathways involved in disease processes is essential for its development as a therapeutic agent.

Biological Activity of 6-ACETYLAMINO-7-AZAINDOLE

Research indicates that compounds similar to N-(1H-Pyrrolo[2,3-b]pyridin-6-yl)acetamide exhibit significant biological activities. These include:

  • Anticancer Properties: Some derivatives of pyrrolo[2,3-b]pyridine have shown promise in inhibiting tumor growth and inducing apoptosis in cancer cells.
  • Antimicrobial Activity: Certain analogs have demonstrated effectiveness against various bacterial strains.
  • Kinase Inhibition: Pyrrolo[2,3-b]pyridine compounds are being investigated for their ability to inhibit specific kinases involved in cancer progression.