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ChemicalBook--->CAS DataBase List--->2754408-94-9

2754408-94-9

2754408-94-9 Structure

2754408-94-9 Structure
IdentificationBack Directory
[Name]

N-(2-chloro-3-((5-chloro-3-methyl-4-oxo-3,4-dihydroquinazolin-6-yl)amino)-4-fluorophenyl)-3-fluoroazetidine-1-sulfonamide
[CAS]

2754408-94-9
[Synonyms]

PF07799933
Claturafenib
N-(2-chloro-3-((5-chloro-3-methyl-4-oxo-3,4-dihydroquinazolin-6-yl)amino)-4-fluorophenyl)-3-fluoroazetidine-1-sulfonamide
N-[2-Chloro-3-[(5-chloro-3,4-dihydro-3-methyl-4-oxo-6-quinazolinyl)amino]-4-fluorophenyl]-3-fluoro-1-azetidinesulfonamide
[Molecular Formula]

C18H15Cl2F2N5O3S
[MOL File]

2754408-94-9.mol
[Molecular Weight]

490.31
Chemical PropertiesBack Directory
[Boiling point ]

585.0±60.0 °C(Predicted)
[density ]

1.72±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
[form ]

Solid
[pka]

6.62±0.40(Predicted)
[color ]

White to light yellow
Hazard InformationBack Directory
[Uses]

Claturafenib ( PF-07799933) is an inhibitor of pan-mutant BRAF. Claturafenib inhibits pERK in HT29 cells with an IC50 value of 1.6 nM[1].
[References]

[1] Rona Yaeger, et al. A Next-Generation BRAF Inhibitor Overcomes Resistance to BRAF Inhibition in Patients with BRAF-Mutant Cancers Using Pharmacokinetics-Informed Dose Escalation. Cancer Discov. 2024 Sep 4;14(9):1599-1611. DOI:10.1158/2159-8290.CD-24-0024
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