Oxy-16

Oxy-16

Catalog Number:
L002373162APE
Mfr. No.:
APE-C5136
Price:
$287
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      • Overview
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          Background

          Oxy-16 is an antagonist of hedgehog activity.
          Naturally occurring oxysterols that are products of cholesterol oxidation can stimulate the hedgehog (Hh) signaling pathway related to cardiovascular disease and bone formation. Activation of Hh signaling modulates inflammatory responses to additional atherogenic factors including lesion-producing macrophages and enable osteoblast differentiation, which is dependent on the target cell.
          In vitro: Oxysterols have been shown to be associated with immunosuppression, apoptosis, atherosclerosis, inflammation, and cholesterol turnover. Other studies aslo indicated that oxysterols were Hedgehog (Hh) signaling pathway activators and had potent osteoinductive properties. Oxy-16, an oxysterol, was identified as a cell permeable oxygenated derivative of cholesterol that might be the end product or intermediate of the cholesterol excretion pathways. Oxy-16 is currently used as a transport form for cholesterol across the blood brain barrier and membranes. The osteogenic differentiation caused by Oxy-16 was cinsidered to be mediated via a Wnt signaling-related, Dkk-1-inhibitable mechanism [1].
          In vivo: Up to now, there is no animal in vivo data reported.
          Clinical trial: So far, no clinical study has been conducted.

      • Properties
        • Categories
          antagonist of hedgehog activity
          Alternative Name
          20(R),22(R)-dihydroxy Cholesterol; cholest-5-ene-3b,20,22R-triol
          CAS Number
          596-94-1
          Molecular Formula
          C27H46O3
          Molecular Weight
          418.7
          Appearance
          A crystalline solid
          Purity
          Purity ≥ 95.00%
          Solubility
          ≤10mg/ml in ethanol;1.5mg/ml in DMSO;1.5mg/ml in dimethyl formamide
          Storage
          Store at -20°C
          SMILES
          O[[email protected]](C1)CC[[email protected]@]2(C)C1=CC[[email protected]]3([H])C2CC[[email protected]@]4(C)[[email protected]@]3([H])CC[[email protected]]4([H])[[email protected]@](C)(O)[[email protected]](O)CCC(C)C

          * For Research Use Only

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