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Exarafenib (KIN-2787) RAF Inhibitor

Cat.No.E1649

Exarafenib(KIN-002787, KIN-2787, RAF/KIN_2787) is an orally-available, selective inhibitor of pan-RAF. Exarafenib is effective in RAF-dependent cancers, including all classes of BRAF alterations. Exarafenib suppresses MAPK signaling in RAF-dependent melanoma cell lines. KIN-2787 exhibits low nanomolar to picomolar potency against RAF1, BRAF, and ARAF with an IC50 of 0.06-3.46 nM with minimal activity towards non-RAF kinases.
Exarafenib (KIN-2787) Raf inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 521.58

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Quality Control

Batch: Purity: 99.10%
99.10

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (191.72 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble

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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Chemical Information, Storage & Stability

Molecular Weight 521.58 Formula

C26H34F3N5O3

Storage (From the date of receipt)
CAS No. 2639957-39-2 Download SDF Storage of Stock Solutions

Mechanism of Action

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04913285 Recruiting
Solid Tumor Adult|Non-small Cell Lung Cancer|Melanoma
Kinnate Biopharma
August 4 2021 Phase 1

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