Delavirdine

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Selleck Chemicals

E7534

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Delavirdine is an inhibitor of Reverse Transcriptase used in studies of Viral Entry / Replication. It is especially relevant in immunology, inflammation, and infectious disease models, where defined compound exposure can be linked to host-pathogen interactions, entry mechanisms, and replication-associated responses.

By inhibiting Reverse Transcriptase, Delavirdine can be used to examine host-pathogen interactions, entry mechanisms, and replication-associated responses. The enzyme annotation adds relevance to enzyme-activity assays, substrate-conversion studies, and mechanism profiling, together with downstream-response mapping in the same experimental setting. In immunology, inflammation, and infectious disease models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.

Research Applications

  • Target-focused assays involving Reverse Transcriptase
  • Pathway perturbation studies connected to Viral Entry / Replication
  • Concentration-response inhibition and target-dependence studies
  • Enzyme-activity assays, substrate-conversion studies, and mechanism profiling

Overall, Delavirdine is appropriate when a defined chemical perturbant is needed to connect Reverse Transcriptase with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in immunology, inflammation, and infectious disease models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.

Targets:
Reverse Transcriptase
Target Class:
Enzyme
Pathways:
Viral Entry / Replication
Research Area:
Immunology • Inflammation • Infectious Disease
CAS No.:
136817-59-9
Molecular Weight:
456.56
SMILES:
CC(C)Nc1cccnc1N1CCN(C(=O)c2cc3cc(NS(C)(=O)=O)ccc3[nH]2)CC1
InChIKey:
WHBIGIKBNXZKFE-UHFFFAOYSA-N
PubChem:
5625
Storage Temperature:
-20°C

For Research Use Only. Not intended for diagnostic or therapeutic use.
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