2011034-27-6

2α-Acetoxy-14,15-cyclopimara-7β,16-diol Chemical Structure
2011034-27-6

Chemical Structure

2α-Acetoxy-14,15-cyclopimara-7β,16-diol

  • CAS. Nr.: 2011034-27-6
  • Formula:C22H36O4
  • Molecular Weight:364.52

InChIKey: PTRMLDRXBSKIGD-VWRGGBKHSA-N

SMILES: C[C@]12[C@]([C@H]2CO)([H])[C@@]3([H])[C@@](CC1)([H])[C@@]4([C@@](C(C)(C[C@@H](C4)OC(C)=O)C)([H])C[C@@H]3O)C

Biological Activity: 2α-Acetoxy-14,15-cyclopimara-7β,16-diol (compound 2) is a potential anti-inflammatory agent, exhibiting weak anti-inflammatory activity by inhibiting inflammation-related NO production. 2α-Acetoxy-14,15-cyclopimara-7β,16-diol only inhibits nitric oxide (NO) production in LPS-induced RAW264.7 macrophages, with an inhibition rate of 28.1%. 2α-Acetoxy-14,15-cyclopimara-7β,16-diol can be naturally extracted from the 70% ethanol extract of the seeds of Caesalpinia minax Hance (a plant of the Caesalpinia genus in the Fabaceae family)[1].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-N13821
2α-Acetoxy-14,15-cyclopimara-7β,16-diol 2α-Acetoxy-14,15-cyclopimara-7β,16-diol (compound 2) is a potential anti-inflammatory agent, exhibiting weak anti-inflammatory activity by inhibiting inflammation-related NO production. 2α-Acetoxy-14,15-cyclopimara-7β,16-diol only inhibits nitric oxide (NO) production in LPS-induced RAW264.7 macrophages, with an inhibition rate of 28.1%. 2α-Acetoxy-14,15-cyclopimara-7β,16-diol can be naturally extracted from the 70% ethanol extract of the seeds of Caesalpinia minax Hance (a plant of the Caesalpinia genus in the Fabaceae family).
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