VEMURAFENIB

Vemurafenib is a BRAF inhibitor used in metastatic melanoma with BRAF V600E mutations. It blocks MAPK signaling to reduce tumor growth. Side effects include rash, photosensitivity, arthralgia, QT prolongation, and secondary skin tumors. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 294d08642e7c Category: Tag:

Product Description


Mechanism of Action

VEMURAFENIB exhibits a highdimensional biochemical interaction matrix spanning signallingaxis disruption, catalyticdomain modulation, mitochondrialnetwork recalibration, ionflux redistribution, cytoskeletalarchitecture remodelling, membranepotential rebalancing and transcriptionfactor pathway restructuring. Its molecular topology supports interaction with catalytic residues, allosteric regulators, transmembrane helices, nucleotidebinding pockets, redoxbuffer modules and polymeric scaffolding complexes, enabling wideband influence across metabolic, structural, genomic and electrophysiological domains.

Mechanistically, VEMURAFENIB may reshape phosphorylation maps across ERK/MAPK/JNK/p38 axes, alter PI3KAKT survivalbias, modulate Gprotein coupling geometry, redistribute Ca²⁺ microdomain waveforms, adjust IP/DAG signalling topology and recalibrate cAMPPKA amplitude. Mitochondrial impacts include ETCcomplex rebalancing, ATP/ADP cycle modulation, ROSthreshold displacement, mitochondrial membranepotential polarity shifts and crossorganelle stress signalling.

HighPrecision

  • Kinomescale interference & catalyticcascade modelling
  • Highresolution docking & conformationalflow prediction
  • UPR/ERstress & autophagy/mitophagy integration networks
  • Full multiomics reconstruction (RNAseq, proteomics, phosphoproteomics, metabolomics)
  • Cytoskeletal forcemapping & polymer turnover dynamics
  • Cellfate modelling: apoptosis, necroptosis, ferroptosis, parthanatos
  • AIdriven SAR/QSAR predictive simulation

Toxicodynamics & Cellular Hazard Spectrum

  • Excessive ROS accumulation & antioxidantbuffer collapse
  • Mitochondrial fragmentation or ETC suppression
  • Hyperdisruption of Na⁺/K⁺/Ca²⁺ ionicgradients
  • Cytoskeletal degradation & membrane-integrity failure
  • Inflammatory masterswitch activation (NF-κB/STAT/IRF)
  • Multiaxis programmed-cell-death induction
  • Epigenetic drift across methylation & acetylation layers

For expert laboratory research only not intended for biological use.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C23H18ClF2N3O3S

Molecular Weight

489.9 g/mol

CAS Number

918504-65-1

Storage Condition

Store at room temperature 20 °C – 25 degC (68 °F – 77 °F); excursions permitted between 15 °C and 30 °C (59 °F and 86 °F), See USP Controlled Room Temperature. Store in the original container with the lid tightly closed.

Solubility

<1 mg/mL

Purity

Purity information is available upon request (COA).

Synonym

Vemurafenib; 918504-65-1; Zelboraf; PLX-4032; PLX 4032

IUPAC/Chemical Name

N-[3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl]propane-1-sulfonamide

InChl Key

GPXBXXGIAQBQNI-UHFFFAOYSA-N

InChl Code

InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31,32)29-19-8-7-18(25)20(21(19)26)22(30)17-12-28-23-16(17)10-14(11-27-23)13-3-5-15(24)6-4-13/h3-8,10-12,29H,2,9H2,1H3,(H,27,28)

References

https://pubchem.ncbi.nlm.nih.gov/compound/42611257;

3D Conformer.

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