Quarfloxin

Quarfloxin
  • Name: Quarfloxin
  • Catalog No.: CPD2205
  • CAS No.: 865311-47-3
  • Molecular Weight: 604.67
  • Chemical Formula: C35H33FN6O3
  • For scientific research only, not for patients.

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    Chemical Name:

    5-fluoro-N-(2-((S)-1-methylpyrrolidin-2-yl)ethyl)-3-oxo-6-((R)-3-(pyrazin-2-yl)pyrrolidin-1-yl)-3H-benzo[b]pyrido[3,2,1-kl]phenoxazine-2-carboxamide

    SMILES Code: 

    FC1=C(N2CC[C@@H](C3=CN=CC=N3)C2)C(OC4=C5C=C6C(C=CC=C6)=C4)=C(N5C=C(C(NCC[C@H]7N(C)CCC7)=O)C8=O)C8=C1

    InChi Code:

    InChI=1S/C35H33FN6O3/c1-40-13-4-7-24(40)8-10-39-35(44)26-20-42-29-15-21-5-2-3-6-22(21)16-30(29)45-34-31(42)25(33(26)43)17-27(36)32(34)41-14-9-23(19-41)28-18-37-11-12-38-28/h2-3,5-6,11-12,15-18,20,23-24H,4,7-10,13-14,19H2,1H3,(H,39,44)/t23-,24+/m1/s1

    InChi Key:

    WOQIDNWTQOYDLF-RPWUZVMVSA-N

    Keyword:

    CX 3543; CX-3543; CX 3543; Quarfloxacin

    Solubility: 

    Storage: 

    Description: 

    Quarfloxin, also known as Quarfloxacin and CX-3543, is a fluoroquinolone derivative with antineoplastic activity. Quarfloxin disrupts the interaction between the nucleolin protein and a G-quadruplex DNA structure in the ribosomal DNA (rDNA) template, a critical interaction for rRNA biogenesis that is overexpressed in cancer cells; disruption of this G-quadruplex DNA:protein interaction in aberrant rRNA biogenesis may result in the inhibition of ribosome synthesis and tumor cell apoptosis.

    Target: 


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