structure of 2-(2-Aminopyrimidin-4-Yl)-5-Morpholinophenol

2-(2-Aminopyrimidin-4-Yl)-5-Morpholinophenol

CAS No.: 1000340-04-4
M. Wt: 272.3
M. Fa: C14H16N4O2
InChI Key: -

Names and Identifiers of 1000340-04-4

CAS Number

1000340-04-4

IUPAC Name

2-(2-azanylpyrimidin-4-yl)-5-morpholin-4-yl-phenol

Canonical SMILES

C1COCCN1C2=CC(=C(C=C2)C3=NC(=NC=C3)N)O

Physical and chemical properties of 1000340-04-4

Molecular Formula

C14H16N4O2

Molecular Weight

272.3

Applications of 1000340-04-4

The applications of 2-(2-Aminopyrimidin-4-YL)-5-morpholinophenol span various fields:

  • Pharmaceutical Development: Explored as a lead compound in drug discovery programs aimed at developing new antimicrobial or anticancer agents.
  • Biochemical Research: Used as a biochemical probe to study specific cellular pathways and enzyme activities.

Its unique structure allows it to serve as a versatile building block for synthesizing more complex molecules with tailored biological activities.

Interaction Studies of 1000340-04-4

Interaction studies focus on understanding how 2-(2-Aminopyrimidin-4-YL)-5-morpholinophenol interacts with biological targets:

  • Enzyme Binding: Investigations into its binding affinity with specific enzymes can reveal its mechanism of action.
  • Receptor Interaction: Studies may also assess how this compound interacts with cellular receptors, influencing signaling pathways involved in disease processes.

These studies are crucial for elucidating the therapeutic potential and optimizing the compound for clinical use.

Similar Compounds

Several compounds share structural similarities with 2-(2-Aminopyrimidin-4-YL)-5-morpholinophenol, including:

  • 2-Cyclopropyl-3H,4H,5H,6H,7H-cyclopenta[d]pyrimidin-4-one
  • 3-Amino-1-methyl-4-(2-thienyl)-1,4,5,7-tetrahydro-6H-pyrrolo[3,4-b]quinolin-6-one
Uniqueness

What distinguishes 2-(2-Aminopyrimidin-4-YL)-5-morpholinophenol from these similar compounds is its specific combination of a pyrimidine ring and morpholine structure. This unique configuration contributes to its distinct biological activities and chemical reactivity profiles compared to other heterocyclic compounds. Its ability to modulate various biological pathways makes it a valuable candidate for further research in medicinal chemistry.

Biological Activity of 1000340-04-4

2-(2-Aminopyrimidin-4-YL)-5-morpholinophenol exhibits a range of biological activities, which may include:

  • Antimicrobial: Potential effectiveness against various bacterial strains.
  • Antiviral: Investigated for activity against viral pathogens.
  • Anticancer: Shows promise in inhibiting cancer cell proliferation through specific molecular interactions.

The biological activity is largely attributed to its ability to interact with enzymes and receptors involved in key metabolic pathways, potentially modulating their function.