ChemicalBook--->CAS DataBase List--->1800398-38-2

1800398-38-2

1800398-38-2 Structure

1800398-38-2 Structure
IdentificationBack Directory
[Name]

LXH254,LXH-254
[CAS]

1800398-38-2
[Synonyms]

LXH254
Naporafenib
LXH254,LXH-254
LXH254; LXH-254; LXH 254
4-Pyridinecarboxamide, N-[3-[2-(2-hydroxyethoxy)-6-(4-morpholinyl)-4-pyridinyl]-4-methylphenyl]-2-(trifluoromethyl)-
[Molecular Formula]

C25H25F3N4O4
[MDL Number]

MFCD31657408
[MOL File]

1800398-38-2.mol
[Molecular Weight]

502.49
Chemical PropertiesBack Directory
[Boiling point ]

601.9±55.0 °C(Predicted)
[density ]

1.353±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:100.0(Max Conc. mg/mL);199.0(Max Conc. mM)
[form ]

A crystalline solid
[pka]

10.86±0.70(Predicted)
[color ]

Off-white to light yellow
[InChIKey]

UEPXBTCUIIGYCY-UHFFFAOYSA-N
[SMILES]

C1(C(F)(F)F)=NC=CC(C(NC2=CC=C(C)C(C3C=C(N4CCOCC4)N=C(OCCO)C=3)=C2)=O)=C1
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

LXH254, is a kinase inhibitor used in the treatment of solid tumors.
[in vivo]

Treatment with Naporafenib (Compound A) generates tumor regression in several KRAS-mutant models including the NSCLC-derived Calu-6 (KRAS Q61K) and NCI-H358 (KRAS G12C). Naporafenib exhibits efficacy in numerous MAPK-driven human cancer cell lines and in xenograft tumors representing model tumors harboring human lesions in KRAS, NRAS and BRAF oncogenes[1].
Naporafenib shows significant antitumor activity in models harboring BRAF mutations either alone or coincident with either activated NRAS or KRAS, and RAS mutants lacking ARAF are more sensitive to Naporafenib[2].

Animal Model:Outbred athymic (nu/nu) female mice and SCID Beige mice; BRAF-, NRAS-, and KRAS-mutant xenograft models, as well as a RAS/RAF wild-type model[2]
Dosage:100 mg/kg
Administration:Orally, daily
Result:Significantly decreased tumor volume in models harboring BRAF mutations either alone or coincident with either activated NRAS or KRAS, slightly decreased tumor volume in KRAS model.
[IC 50]

CRAF: 0.072 nM (IC50); Braf: 0.21 nM (IC50); ARAF: 6.4 nM (IC50); p38α: 2.1 μM (IC50); Abl1: 4.9 μM (IC50)
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

LXH254,LXH-254(1800398-38-2)1HNMR
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