Cholestenone

CAS No. 601-57-0

Cholestenone ( (+)-4-Cholesten-3-one )

Catalog No. M19974 CAS No. 601-57-0

4-Cholesten-3-one is an intestinal metabolite of Cholesterol. It shows an anti-obesity effect on animals.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 52 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Cholestenone
  • Note
    Research use only not for human use.
  • Brief Description
    4-Cholesten-3-one is an intestinal metabolite of Cholesterol. It shows an anti-obesity effect on animals.
  • Description
    4-Cholesten-3-one is an intestinal metabolite of Cholesterol. It shows an anti-obesity effect on animals.
  • Synonyms
    (+)-4-Cholesten-3-one
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    601-57-0
  • Formula Weight
    384.64
  • Molecular Formula
    C27H44O
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 2 mg/mL
  • SMILES
    CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Rosenheim O et al. The mechanism of coprosterol formation in vivo: 1. Cholestenone as an intermediate. Biochem J. 1943 Oct;37(4):513-4.
molnova catalog
related products
  • 2,4,5-Trichloro-7H-p...

    2,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid is a chemical agent.

  • (Z)-Ferulic acid 4-O...

    cis-Ferulic acid 4-O-β-D-glucopyranoside (compound 7) is a phenolic glycosid, which can be isolated from Nitraria sibirica.

  • OD1

    Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases peak currents at all voltages and stimulates a persistent Na+ current at hNav1.7 channel. Increases hyperpolarization at Nav1.4 and Nav1.6 channels. Induces spontaneous pain in vivo.