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1516772-44-3

1516772-44-3 Structure

1516772-44-3 Structure
IdentificationBack Directory
[Name]

AZ-27
[CAS]

1516772-44-3
[Synonyms]

AZ-27
4H-Thieno[3,2-d][1]benzazepine-2-carboxamide, N-cyclopropyl-5,6-dihydro-6-[4-[[[2-(2-oxa-7-azaspiro[3.5]non-7-yl)-3-pyridinyl]carbonyl]amino]benzoyl]-
[Molecular Formula]

C36H35N5O4S
[MOL File]

1516772-44-3.mol
[Molecular Weight]

633.76
Chemical PropertiesBack Directory
[Boiling point ]

840.3±65.0 °C(Predicted)
[density ]

1.43±0.1 g/cm3(Predicted)
[pka]

11.60±0.70(Predicted)
Hazard InformationBack Directory
[Uses]

N-Cyclopropyl-5,6-dihydro-6-[4-[[[2-(2-oxa-7-azaspiro[3.5]non-7-yl)-3-pyridinyl]carbonyl]amino]benzoyl]-4H-thieno[3,2-d][1]benzazepine-2-carboxamide is a possible respiratory syncytial virus (RSV) RNA polymerase inhibitor.
[Enzyme inhibitor]

This RSV inhibitor (FW = 633.77 g/mol) targets Respiratory Syncytial Virus, inhibiting both mRNA transcription and genome replication in cell based mini-genome assays, suggesting it targets a step common to both of these RNA synthesis processes. Analysis in an in vitro transcription run-on assay, containing RSV nucleocapsids, showed that AZ-27 inhibits (IC50 ≈ 15 nM) the synthesis of transcripts from the 3′-end of the genome to a greater extent than those from the 5′-end, indicating that it inhibits transcription initiation. In experiments assaying polymerase activity on the promoter, AZ-27 inhibits transcription and replication initiation. The RSV polymerase also utilizes the promoter sequence to perform a back-priming reaction. Addition of AZ-27 has no effect on the addition of up to three nucleotides by back-priming, but inhibits further extension of the back primed RNA. These findings suggest that the RSV polymerase is likely to adopt different conformations to execute its separate functions at the promoter.
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