1. Membrane Transporter/Ion Channel
  2. P-glycoprotein
  3. Ceefourin 2

Ceefourin 2 is a potent and highly selective inhibitor of MRP4. Ceefourin 2 inhibits the transport of MRP4 substrates but is not selective for other ABC transporters. Ceefourin 2 shows lower cytotoxicity and higher microsomal and acid stability.

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Ceefourin 2

Ceefourin 2 Chemical Structure

CAS No. : 348148-51-6

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Description

Ceefourin 2 is a potent and highly selective inhibitor of MRP4. Ceefourin 2 inhibits the transport of MRP4 substrates but is not selective for other ABC transporters. Ceefourin 2 shows lower cytotoxicity and higher microsomal and acid stability[1].

In Vitro

Ceefourin 2 is highly selective for MRP4 over other ABC transporters, including P-glycoprotein (P-gp), ABCG2 (Breast Cancer Resistance Protein; BCRP) and MRP1 (ABCC1). Ceefourin 2 has limited off-target effects and high stability[1].
Ceefourin 2 (100 nM-100 μM) has low cellular toxicity (IC50 >50 μM) in two normal (HSF, MRC5), five neuroblastoma (BE(2)-C, IMR-32, IMR-32, SK-N-SH, SHEP) and four other human cancer cell lines (HEPG2, LNCap, SJ-G2, MCF7)[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

355.70

Formula

C15H9ClF3N3O2

CAS No.
Appearance

Solid

Color

Light yellow to brown

SMILES

O=C(O)C1=NN2C(C(F)(F)F)=CC(C3=CC=C(C=C3)C)=NC2=C1Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation
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Ceefourin 2
Cat. No.:
HY-121088
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