154844-26-5

Basic information

• Product Name: 1-PHENYL-2-(PHENYLAMINO)-5-D-RIBOFURANOSYL-4(1H)-PYRIMIDINONE
• Synonyms: 1-PHENYL-2-(PHENYLAMINO)-5-D-RIBOFURANOSYL-4(1H)-PYRIMIDINONE
• CAS NO: 154844-26-5
• Molecular Formula: C21H21N3O5
• Molecular Weight: 395.41
• Mol File: 154844-26-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 636.7±65.0 °C(Predicted)
• Appearance: /
• Density: 1.45±0.1 g/cm3(Predicted)
• PKA: 13.37±0.70(Predicted)
• CAS DataBase Reference: 1-PHENYL-2-(PHENYLAMINO)-5-D-RIBOFURANOSYL-4(1H)-PYRIMIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PHENYL-2-(PHENYLAMINO)-5-D-RIBOFURANOSYL-4(1H)-PYRIMIDINONE(154844-26-5)
• EPA Substance Registry System: 1-PHENYL-2-(PHENYLAMINO)-5-D-RIBOFURANOSYL-4(1H)-PYRIMIDINONE(154844-26-5)

Safety Data

• Hazardous Substances Data: 154844-26-5(Hazardous Substances Data)

Usage

Explanation

This is the chemical name of the compound, which is also known as PAP.

Explanation

PAP belongs to a class of chemical compounds called ribofuranosylpyrimidinone derivatives.

Explanation

PAP contains a phenylamino group, which is a key functional group in its molecular structure.

Explanation

PAP has been studied for its potential to inhibit viral replication, making it a candidate for antiviral drug development.

Explanation

PAP is believed to work by inhibiting the activity of reverse transcriptase, an enzyme used by viruses like HIV to replicate their genetic material.

Explanation

PAP has been investigated for its potential use in the treatment of HIV and other viral infections, with ongoing research to further explore its antiviral properties.

Explanation

The potential of PAP in the development of new antiviral medications is currently being explored due to its promising antiviral activity.

Type

Ribofuranosylpyrimidinone derivative

Functional group

Phenylamino group

Potential use

Antiviral properties

Target enzyme

Reverse transcriptase

Research focus

HIV and other viral infections

Development

New antiviral medications