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262433-54-5

262433-54-5 Structure

262433-54-5 Structure
IdentificationBack Directory
[Name]

BENZOIC ACID, 3-FLUORO-4-[[(2R)-HYDROXY(5,6,7,8-TETRAHYDRO-5,5,8,8-TETRAMETHYL-2-NAPHTHALENYL)ACETYL]AMINO]-
[CAS]

262433-54-5
[Synonyms]

Benzoic acid, 3-fluoro-4-[[(2R)-2-hydroxy-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)acetyl]amino]-
[Molecular Formula]

C23H26FNO4
[MDL Number]

MFCD10565938
[MOL File]

262433-54-5.mol
[Molecular Weight]

399.46
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

DMSO: 20 mg/ml
[form ]

A solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

BMS270394 is a nuclear retinoic acid receptor (RAR-γ) agonist with the EC50 values of 30 nM and 400 nM for humanRAR-γ and RAR-β, respectively[1].
[Biological Activity]

BMS 270394 is an agonist of retinoic acid receptor γ (RARγ; EC50 = 30 nM in a transactivation assay) and the active enantiomer of BMS 189961 .1 It is selective for RARγ over RARβ (EC50 = 400 nM) and is inactive at RARα. BMS 270394 synergizes with paclitaxel to inhibit the growth of MCF-7 breast and OVCAR-3 ovarian cancer, as well as SqCC/Y1 head and neck squamous cell carcinoma, cells.2
[IC 50]

RXR γ: 30 nM (EC50); RXR β: 400 nM (EC50)
[storage]

-20°C
[References]

1.Klaholz, B.P., Mitschler, A., Belema, M., et al.Enantiomer discrimination illustrated by high-resolution crystal structures of the human nuclear receptor hRARγProc. Natl. Acad. Sci. USA97(12)6322-6327(2000) 2.Vivat-Hannah, V., You, D., Rizzo, C., et al.Synergistic cytotoxicity exhibited by combination treatment of selective retinoid ligands with taxol (Paclitaxel)Cancer Res.61(24)8703-8711(2001)
262433-54-5 suppliers list
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Tags:262433-54-5 Related Product Information
185629-22-5

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