TNP-351

CAS No. 125991-51-7

TNP-351( TNP351 )

Catalog No. M11069 CAS No. 125991-51-7

TNP-351 is an antifolate compound that functions as a DHFR inhibitor, strongly inhibits the growth of Meth A cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    TNP-351
  • Note
    Research use only, not for human use.
  • Brief Description
    TNP-351 is an antifolate compound that functions as a DHFR inhibitor, strongly inhibits the growth of Meth A cells.
  • Description
    TNP-351 is an antifolate compound that functions as a DHFR inhibitor, strongly inhibits the growth of Meth A cells.
  • In Vitro
    TNP-351 inhibits the proliferation of mouse L1210 leukemia cells and human CCRF-CEM lymphoblastic leukemia cells with ED50 values of 0.79 and 2.7 nM, respectively. The ED50 values determined for the parent cell line CCRF-CEM, CCRFCEM R30/6 subline, CCRF-CEM R1, and CCRF-CEM R2 are 2.7, 5.8, 94 and 76 nM, respectively. Cell Viability Assay Cell Line:L1210 and CCRF-CEM cells Concentration:0.1, 0.3, 1, 3, and 10 nM for L1210 cells; 0.3, 1, 3, 10, and 30 for CCRF-CEM cells Incubation Time:48 hours for L1210 cells; 72 hours for CCRF-CEM cells Result:The ED50 values were 0.79 and 2.7 nM for L1210 and CCRF-CEM cells, respectively.
  • In Vivo
    ——
  • Synonyms
    TNP351
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Antifolate
  • Recptor
    Antifolate
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    125991-51-7
  • Formula Weight
    440.46
  • Molecular Formula
    C21H24N6O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(O)CC[C@@H](C(O)=O)NC(C1=CC=C(CCCC2=CN=C3NC(N)=NC(N)=C32)C=C1)=O
  • Chemical Name
    (2S)-2-[[4-[3-(2,4-diamino-7H-pyrrolo[2,3-d]pyrimidin-5-yl)propyl]benzoyl]amino]pentanedioic acid

Shipping & Storage Information

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

Reference

1. Itoh F, et al. Cancer Chemother Pharmacol. 1994;34(4):273-9. 2. Itoh F, et al. Chem Pharm Bull (Tokyo). 1995 Feb;43(2):230-5.
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