HHQ

CAS No. 40522-46-1

HHQ( 2-heptylquinolin-4(1H)-one )

Catalog No. M27134 CAS No. 40522-46-1

HHQ is a PqsR antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 104 Get Quote
10MG 167 Get Quote
25MG 268 Get Quote
50MG 381 Get Quote
100MG 564 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    HHQ
  • Note
    Research use only, not for human use.
  • Brief Description
    HHQ is a PqsR antagonist.
  • Description
    HHQ is a PqsR antagonist.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    2-heptylquinolin-4(1H)-one
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Apoptosis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    40522-46-1
  • Formula Weight
    243.35
  • Molecular Formula
    C16H21NO
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CCCCCCCc1cc(=O)c2ccccc2[nH]1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Wu W, et, al. Millepachine showed novel antitumor effects in cisplatin-resistant human ovarian cancer through inhibiting drug efflux function of ATP-binding cassette transporters. Phytother Res. 2018 Dec; 32(12):2428-2435.
molnova catalog
related products
  • Calcitonin, porcine

    Calcitonin, porcine inhibits 1,25 (OH)2D3-stimulated porcine osteoclast differentiation. Calcitonin is a polypeptide hormone that can lower serum calcium by decreasing calcium reabsorption in the kidney and inhibiting osteoclastic bone resorption. Calcitonin, porcine can be used for research of hypercalcemia.

  • Platelet-Derived Gro...

    Platelet-Derived Growth Factor Receptor Substrate 1; PDGF Receptor Substrate

  • AC1NS4RE

    SU5614 is a potent and selective FLT3 inhibitor. SU5614 has inhibitory activity for FLT3 and selectively induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3.