REMDESIVIR

Remdesivir is a nucleotide analog inhibiting viral RNA‑dependent RNA polymerase, used for COVID‑19 and other RNA viruses. Side effects include elevated liver enzymes, nausea, hypersensitivity reactions, and rare renal effects.

Product Description


Mechanism of Action

REMDESIVIR (ID 29756) displays a high‑dimensional biochemical interaction profile, integrating catalytic‑domain modulation, multi‑axis signalling interference, mitochondrial‑network recalibration, ion‑flux redistribution, membrane‑potential rebalancing, cytoskeletal remodelling, redox‑equilibrium restructuring and transcription‑factor pathway reprogramming. Its molecular topology supports interaction with catalytic residues, allosteric microdomains, transmembrane helices, nucleotide‑binding pockets, redox‑buffer centres and polymeric scaffolding complexes, enabling wide‑band influence across metabolic, genomic, structural and electrophysiological layers.

At the signalling level, REMDESIVIR may reconfigure phosphorylation landscapes spanning ERK/MAPK/JNK/p38 and PI3K–AKT axes, modulate G‑protein coupling states, reorganise Ca²⁺ microdomain geometry, adjust IP₃/DAG cascade topology, and recalibrate cAMP–PKA amplitude distributions. Mitochondrial effects can include ETC‑complex rebalancing, ATP/ADP flux modulation, ROS‑threshold displacement, membrane‑potential polarity shifts and bidirectional stress‑signal integration between ER and mitochondrial compartments.

Advanced Research Applications

  • Kinome‑scale catalytic‑cascade interference mapping
  • High‑resolution docking & conformational‑transition simulations
  • UPR/ER‑stress, mitophagy & autophagic‑flux network analysis
  • Full multi‑omics integration (RNA‑seq, proteomics, phosphoproteomics, metabolomics)
  • Cytoskeletal mechanics & polymer‑turnover/force‑distribution modelling
  • Cell‑fate pathway simulations (apoptosis, necroptosis, ferroptosis, parthanatos)
  • AI‑driven SAR/QSAR pipelines for compound‑performance prediction

Toxicodynamics & Hazard Spectrum

  • Rapid ROS escalation & antioxidant‑buffer saturation
  • Mitochondrial fragmentation or ETC‑axis suppression
  • Severe Na⁺/K⁺/Ca²⁺ ionic‑flux destabilisation
  • Cytoskeletal depolymerisation & membrane‑integrity loss
  • Hyperactivation of NF‑κB, STAT & IRF inflammatory regulators
  • Induction of multi‑axis programmed‑cell‑death pathways
  • Epigenetic drift including methylation/acetylation imbalance

For expert laboratory research only — not intended for biological or therapeutic exposure.

Datasheet


Molecular Formula

C27H35N6O8P

Molecular Weight

602.6 g/mol

CAS Number

1809249-37-3

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Remdesivir; 1809249-37-3; GS-5734; Veklury; 3QKI37EEHE

IUPAC/Chemical Name

2-ethylbutyl (2S)-2-[[[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxyoxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate

InChl Key

RWWYLEGWBNMMLJ-YSOARWBDSA-N

InChl Code

InChI=1S/C27H35N6O8P/c1-4-18(5-2)13-38-26(36)17(3)32-42(37,41-19-9-7-6-8-10-19)39-14-21-23(34)24(35)27(15-28,40-21)22-12-11-20-25(29)30-16-31-33(20)22/h6-12,16-18,21,23-24,34-35H,4-5,13-14H2,1-3H3,(H,32,37)(H2,29,30,31)/t17-,21+,23+,24+,27-,42-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/121304016;

3D Conformer.

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