179388-53-5
Chemical Structure
Macrocarpal H
- CAS No.: 179388-53-5
- Formula:C28H40O6
- Molecular Weight:472.61
IUPAC Name: 2,4,6-trihydroxy-5-((S)-1-((1S,4aS,6R,8aS)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylenedecahydronaphthalen-1-yl)-3-methylbutyl)isophthalaldehyde
InChIKey: OOAOETHJYYAVCC-GNLPDQNGSA-N
SMILES: CC(C)C[C@H](C1=C(C(C=O)=C(O)C(C=O)=C1O)O)[C@@]2([H])[C@]3([C@@](C(CC2)=C)([H])C[C@H](C(C)(O)C)CC3)C
Biological Activity: Macrocarpal H is a natural compound that can be isolated from the Leaves of Eucalyptus globulus. Macrocarpal H exhibits antibacterial activity against Gram-positive cariogenic bacteria and Gram-negative periodontopathic bacteria. Macrocarpal H inhibits adherent water-insoluble glucan synthesis via glucosyltransferase. Macrocarpal H can be used for the research of caries, periodontal disease, dental caries, periodontal disorders[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Macrocarpal H | 73.0% | Macrocarpal H is a natural compound that can be isolated from the Leaves of Eucalyptus globulus. Macrocarpal H exhibits antibacterial activity against Gram-positive cariogenic bacteria and Gram-negative periodontopathic bacteria. Macrocarpal H inhibits adherent water-insoluble glucan synthesis via glucosyltransferase. Macrocarpal H can be used for the research of caries, periodontal disease, dental caries, periodontal disorders. | ||||||||||||||||||||
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References
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[1]. Kenji OSAWA, et al. Configuraitonal and Conformational Analysis of Macrocarpals H, I, and J from Eucalyptus globulus. Chemical and Pharmaceutical Bulletin. 1997, Volume 45, Issue 7, Pages 1216-1217.
- [2]. Osawa K, et al. Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus. J Nat Prod. 1996 Sep;59(9):823-7. [Content Brief]
