560-09-8

(-)-Camphoric acid Chemical Structure
560-09-8

Chemical Structure

(-)-Camphoric acid

  • CAS. Nr.: 560-09-8
  • Formula:C10H16O4
  • Molecular Weight:200.23

IUPAC Name: (1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid

InChIKey: LSPHULWDVZXLIL-QUBYGPBYSA-N

SMILES: O=C([C@]1(C)C(C)(C)[C@H](C(O)=O)CC1)O

Biological Activity: (-)-Camphoric acid is the less active enantiomer of Camphoric acid. Camphoric acid induces glutamate receptor expression. Camphoric acid also significantly induces the activation of NF-κB and AP-1. Camphoric acid significantly stimulates the differentiation of mouse osteoblastic MC3T3-E1 subclone 4 cells. Camphoric acid has weak regulatory function towards glutamate receptors. Camphoric acid can induce mRNA expression of glutamate signaling molecules and activate transcription factors, thereby stimulating osteoblast differentiation[1][2].

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HY-122808
(-)-Camphoric acid 99.91% (-)-Camphoric acid is the less active enantiomer of Camphoric acid. Camphoric acid induces glutamate receptor expression. Camphoric acid also significantly induces the activation of NF-κB and AP-1. Camphoric acid significantly stimulates the differentiation of mouse osteoblastic MC3T3-E1 subclone 4 cells. Camphoric acid has weak regulatory function towards glutamate receptors. Camphoric acid can induce mRNA expression of glutamate signaling molecules and activate transcription factors, thereby stimulating osteoblast differentiation.
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