(1R,7aR)-7-((((R)-2,3-dihydroxy-2-((S)-1-hydroxyethyl)-3-methylbutanoyl)oxy)methyl)-1-(((Z)-2-methylbut-2-enoyl)oxy)-1,2,3,4,5,7a-hexahydropyrrolizine 4-oxide - Names and Identifiers
Name | (+)-Echimidine N-Oxide
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Synonyms | Echimidin-N-oxid N-Oxid des Asprumines (+)-Echimidine N-Oxide (+)-EchiMidine N-Oxide KDJGEXAPDZNXSD-KCFAIRMISA-N (1R,7aR)-7-((((R)-2,3-dihydroxy-2-((S)-1-hydroxyethyl)-3-methylbutanoyl)oxy)methyl)-1-(((Z)-2-methylbut-2-enoyl)oxy)-1,2,3,4,5,7a-hexahydropyrrolizine 4-oxide L-threo-Pentitol, 1,5-dideoxy-2-C-methyl-3-C-[[[(1R,7aR)-2,3,5,7a-tetrahydro-1-[[(2Z)-2-methyl-1-oxo-2-buten-1-yl]oxy]-4-oxido-1H-pyrrolizin-7-yl]methoxy]carbonyl]-
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CAS | 41093-89-4
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(1R,7aR)-7-((((R)-2,3-dihydroxy-2-((S)-1-hydroxyethyl)-3-methylbutanoyl)oxy)methyl)-1-(((Z)-2-methylbut-2-enoyl)oxy)-1,2,3,4,5,7a-hexahydropyrrolizine 4-oxide - Physico-chemical Properties
Molecular Formula | C20H31NO8
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Molar Mass | 413.47 |
Melting Point | 164-165 °C |
Solubility | Chloroform (Slightly), Methanol (Slightly) |
Appearance | Solid |
Color | White to Off-White |
pKa | 12.41±0.29(Predicted) |
Storage Condition | Amber Vial, -86°C Freezer, Under inert atmosphere |
Stability | Light Sensitive |
(1R,7aR)-7-((((R)-2,3-dihydroxy-2-((S)-1-hydroxyethyl)-3-methylbutanoyl)oxy)methyl)-1-(((Z)-2-methylbut-2-enoyl)oxy)-1,2,3,4,5,7a-hexahydropyrrolizine 4-oxide - Introduction
()-Echimidine N-Oxide, also known as ()-Echimidine N-Oxide, is a plant secondary metabolite with the molecular formula C35H47NO7. It is a natural product with a complex structure, often in the form of white crystals or colorless solids.
( )-Echimidine N-Oxide has antibacterial, anti-inflammatory and anti-tumor pharmacological activities. It is widely used in medical research, especially in the field of anti-tumor has potential application value. It can inhibit the growth of tumor cells by binding with intracellular DNA to affect cell division and proliferation. In addition,( )-Echimidine N-Oxide also has analgesic and neuroprotective effects.
( )-Echimidine N-Oxide is generally obtained by extraction and purification from plants of the genus Cyanthus. Extraction methods may use solvent extraction or Solid Phase Microextraction techniques. Subsequently, purification and separation are carried out by using chromatographic techniques such as gel filtration chromatography and high performance liquid chromatography.
Regarding safety, the current toxicological and pharmacological data of ()-Echimidine N-Oxide are still limited, so the understanding of its safety and toxicity is still limited. When using and handling ()-Echimidine N-Oxide, follow laboratory safety procedures and take necessary personal protective measures.
In summary,( )-Echimidine N-Oxide has a wide range of pharmacological activities and potential medicinal value, but the research on its properties and safety is still in progress.
Last Update:2024-04-09 21:54:55