LSN 3213128

CAS No. 1941211-99-9

LSN 3213128( LSN3213128 )

Catalog No. M13043 CAS No. 1941211-99-9

LSN 3213128 is a novel potent, selective and orally-bioavailable antifolate with potent and specific inhibitory activity for AICARFT.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 336 Get Quote
50MG 1674 Get Quote
100MG 2250 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
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Biological Information

  • Product Name
    LSN 3213128
  • Note
    Research use only, not for human use.
  • Brief Description
    LSN 3213128 is a novel potent, selective and orally-bioavailable antifolate with potent and specific inhibitory activity for AICARFT.
  • Description
    LSN 3213128 is a novel potent, selective and orally-bioavailable antifolate with potent and specific inhibitory activity for AICARFT; results in dramatic elevation of 5-aminoimidazole 4-carboxamide ribonucleotide (ZMP) and growth inhibition in NCI-H460 and MDA-MB-231met2 cancer cell lines; demonstrates tumor growth inhibition in a murine based xenograft model of triple negative breast cancer (TNBC); Aminoimidazole-4-carboxamide ribonucleotide formyltransferase (AICARFT) is an enzyme in the purine biosynthetic pathway.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    LSN3213128
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Antifolate
  • Recptor
    Antifolate
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1941211-99-9
  • Formula Weight
    409.45
  • Molecular Formula
    C17H16FN3O4S2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 62.5 mg/mL (152.64 mM)
  • SMILES
    O=S(C1=CC=C(N2C[C@H](O)CC2)S1)(NC3=CC4=C(C=C3F)C=CNC4=O)=O
  • Chemical Name
    N-(6-Fluoro-1-oxo-1,2-dihydroisoquinolin-7-yl)-5-[(3R)-3-hydroxypyrrolidin-1-yl]thiophene-2-sulfonamide

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Fales KR, et al. J Med Chem. 2017 Oct 26. doi: 10.1021/acs.jmedchem.7b01046.
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