structure of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

CAS No.: 1000340-88-4
M. Wt: 148.162
M. Fa: C8H8N2O
InChI Key: NOPDTQDTGCBXNM-UHFFFAOYSA-N

Names and Identifiers of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

CAS Number

1000340-88-4

IUPAC Name

6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

InChI

InChI=1S/C8H8N2O/c1-5-7(11)4-6-2-3-9-8(6)10-5/h2-4,11H,1H3,(H,9,10)

InChIKey

NOPDTQDTGCBXNM-UHFFFAOYSA-N

Canonical SMILES

CC1=C(C=C2C=CNC2=N1)O

Physical and chemical properties of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

Density

1.3±0.1 g/cm3

Exact Mass

148.063660

Index of Refraction

1.719

LogP

1.84

Molecular Formula

C8H8N2O

Molecular Weight

148.162

PSA

48.91000

Safety Information of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

Pictograms

Signal Word

 Warning

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

Applications of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol has several applications across various fields:

  • Medicinal Chemistry: It serves as a building block in the synthesis of more complex heterocyclic compounds with potential therapeutic effects.
  • Material Science: The compound is explored for its role in developing new materials due to its unique chemical properties.
  • Pharmaceutical Development: Derivatives of this compound are being investigated as potential inhibitors for specific enzymes, making them candidates for drug formulations.

Interaction Studies of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

Studies on the interactions of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol with biological targets are ongoing. Its mechanism of action involves binding to active sites of enzymes, thereby inhibiting their functions. This property is crucial for understanding how this compound can be utilized in therapeutic contexts. Research continues to explore its binding affinities and interactions with other biomolecules, which may elucidate its potential uses in treating various diseases.

Biological Activity of 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

Research indicates that 6-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol exhibits significant biological activities. Studies have highlighted its potential antimicrobial and anticancer properties. The compound has been noted for its ability to inhibit specific enzymes, suggesting its utility as a lead compound in drug development. Its interactions with various biological targets are being explored to understand its mechanism of action and therapeutic potential.