6-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid
Names and Identifiers of 1000342-19-7
CAS Number |
1000342-19-7 |
|---|---|
MDL Number |
MFCD09750008 |
IUPAC Name |
6-methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid |
InChI |
InChI=1S/C9H8N2O2/c1-5-2-8-6(3-10-5)7(4-11-8)9(12)13/h2-4,11H,1H3,(H,12,13) |
InChIKey |
VCWDSSJFLLOJPG-UHFFFAOYSA-N |
Canonical SMILES |
CC1=CC2=C(C=N1)C(=CN2)C(=O)O |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000342-19-7
Boiling Point |
436.7±40.0 °C at 760 mmHg |
|---|---|
Density |
1.4±0.1 g/cm3 |
Exact Mass |
176.058578 |
Flash Point |
217.9±27.3 °C |
H Bond Acceptors |
3 |
H Bond Donors |
2 |
Index of Refraction |
1.709 |
LogP |
0.96 |
Molecular Formula |
C9H8N2O2 |
Molecular Weight |
176.172 |
PSA |
65.98000 |
Vapour Pressure |
0.0±1.1 mmHg at 25°C |
Safety Information of 1000342-19-7
Applications of 1000342-19-7
The applications of 6-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid span various fields:
- Medicinal Chemistry: Investigated as a potential therapeutic agent targeting FGFRs in cancer treatment.
- Organic Synthesis: Used as a building block for developing complex organic molecules.
- Material Science: Explored for its properties in creating new materials and chemical processes.
Interaction Studies of 1000342-19-7
Studies on the interactions of 6-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid have highlighted its specificity towards FGFRs. The compound has been shown to inhibit FGFR activity effectively, leading to reduced proliferation of cancer cells and triggering apoptotic pathways. Further research is ongoing to elucidate the full spectrum of its interactions with other biomolecules and its potential side effects in therapeutic contexts.
Biological Activity of 1000342-19-7
6-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid has been investigated for its interaction with Fibroblast Growth Factor Receptors (FGFRs), particularly acting as an inhibitor at the colchicine-binding site. This inhibition is associated with potent anticancer activities, affecting cell proliferation and inducing apoptosis in cancer cell lines such as breast cancer. The compound's ability to modulate key signaling pathways makes it a candidate for further research in therapeutic applications.
