CAS 92691-35-5
:(+)-Germacrone-4,5-epoxide
Description:
(+)-Germacrone-4,5-epoxide is a bicyclic monoterpene epoxide derived from germacrone, a compound commonly found in various essential oils. This substance is characterized by its epoxide functional group, which contributes to its reactivity and potential biological activity. The molecular structure features a fused ring system, typical of many terpenes, which can influence its physical properties such as boiling point and solubility. (+)-Germacrone-4,5-epoxide is known for its potential applications in the fields of perfumery and flavoring, as well as its possible therapeutic properties, including antimicrobial and anti-inflammatory effects. Its stereochemistry, indicated by the (+) designation, suggests a specific spatial arrangement of atoms that can affect its interaction with biological systems. As with many natural products, the compound may exhibit a range of biological activities, making it of interest for further research in pharmacology and natural product chemistry. Safety and handling precautions should be observed due to the reactive nature of epoxides.
Formula:C15H22O2
InChI:InChI=1S/C15H22O2/c1-10(2)12-9-14-15(4,17-14)7-5-6-11(3)8-13(12)16/h6,14H,5,7-9H2,1-4H3/b11-6+/t14-,15-/m0/s1
InChI key:InChIKey=DWGVRYKQVZGSIB-NCKTXVJMSA-N
SMILES:C[C@]12[C@@](O1)(CC(=C(C)C)C(=O)C\C(\C)=C\CC2)[H]
Synonyms:- (+)-Germacrone-4,5-epoxide
- (1S,6E,10S)-6,10-Dimethyl-3-(1-methylethylidene)-11-oxabicyclo[8.1.0]undec-6-en-4-one
- (4S,5S)-(+)-Germacrone 4,5-epoxide
- 11-Oxabicyclo[8.1.0]undec-6-en-4-one, 6,10-dimethyl-3-(1-methylethylidene)-, [1S-(1R*,6E,10R*)]-
- 11-Oxabicyclo[8.1.0]undec-6-en-4-one, 6,10-dimethyl-3-(1-methylethylidene)-, (1S,6E,10S)-
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Found 3 products.
Germacrone 4,5-epoxide
CAS:(4S,5S)-(+)-Germacrone-4,5-epoxide inhibits certain subtypes of cytochrome P450 (CYP).Formula:C15H22O2Purity:98%Color and Shape:SolidMolecular weight:234.33(4S,5S)-(+)-Germacrone 4,5-epoxide
CAS:<p>(4S,5S)-(+)-Germacrone 4,5-epoxide is a chiral epoxide compound, which is a naturally occurring derivative of germacrone, primarily sourced from various plant species within the Zingiberaceae family. This compound is known for its unique stereochemistry, which imparts specific bioactive properties inherent to its molecular structure. The formation of the epoxide ring in (4S,5S)-(+)-Germacrone 4,5-epoxide facilitates interactions with biological macromolecules, potentially modulating enzymatic activity or disrupting cellular signaling pathways through covalent binding or stereoselective interactions.</p>Formula:C15H22O2Purity:Min. 95%Molecular weight:234.33 g/mol


