A-357300

CAS No. 369358-07-6

A-357300( A357300 )

Catalog No. M14270 CAS No. 369358-07-6

A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    A-357300
  • Note
    Research use only, not for human use.
  • Brief Description
    A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM.
  • Description
    A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM, does not inhibit MetAP1 or leucine aminopeptidases at 10 uM; suppresses tumor growth preclinically without the toxicities observed with TNP-470, induces cytostasis by cell cycle arrest at the G(1) phase selectively in endothelial cells and in a subset of tumor cells, but not in most primary cells of nonendothelial type; inhibits angiogenesis both in vitro and in vivo and shows potent antitumor efficacy in carcinoma, sarcoma, and neuroblastoma murine models.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    A357300
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Aminopeptidase
  • Recptor
    Aminopeptidase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    369358-07-6
  • Formula Weight
    359.869
  • Molecular Formula
    C15H22ClN3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(NNC([C@@H](O)[C@H](N)CCSC(C)C)=O)C1=CC=CC(Cl)=C1
  • Chemical Name
    N'-((2S,3R)-3-amino-2-hydroxy-5-(isopropylthio)pentanoyl)-3-chlorobenzohydrazide

Shipping & Storage Information

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

Reference

1. Wang J, et al. Cancer Res. 2003 Nov 15;63(22):7861-9. 2. Sheppard GS, et al. Bioorg Med Chem Lett. 2004 Feb 23;14(4):865-8. 3. Morowitz MJ, et al. Clin Cancer Res. 2005 Apr 1;11(7):2680-5.
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