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Art. -Nr.: HY-N3666

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Cycloeucalenol

(Synonyms: 3β-Cycloeucalenol)

1 Cited Publications

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Cycloeucalenol is a triterpenoid compound derived from Eucalyptus microcorys.

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Reinheit: 97.0%
CAS. Nr.: 469-39-6
Formel: C₃₀H₅₀O
Molecular Weight:426.72

Speicherung:

-20°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Cycloeucalenol Chemical Structure

CAS. Nr.: 469-39-6

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- Cellular Effect
Chemical Information
Publications (1)
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Bioz

Biologische Aktivität

Beschreibung

Cycloeucalenol is a triterpenoid compound derived from Eucalyptus microcorys^[1].

Cellular Effect

Cell Line	Type	Value	Description	References
Raji	IC₅₀	8.9 nM Compound: 35	Inhibition of TPA-induced Epstein-Barr virus early antigen activation in Raji cells after 48 hrs Inhibition of TPA-induced Epstein-Barr virus early antigen activation in Raji cells after 48 hrs	[PMID: 17503850]

Chemical Information

CAS. Nr. 469-39-6
Appearance Solid
Molecular Weight 426.72
Formel C₃₀H₅₀O
Color White to off-white
SMILES

C[C@]12[C@@]3([H])[C@@]4(CC[C@@]1([C@@](CC2)([H])[C@H](C)CCC(C(C)C)=C)C)[C@@]5([C@@]([C@@H]([C@H](CC5)O)C)([H])CC3)C4
Synonyms

3β-Cycloeucalenol
Structure Classification
- Terpenoids
- Triterpenes
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

-20°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Publications (1)

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Plant J

Unveiling the inequivalent biochemical functions of OsSMO2-1 and OsSMO2-2 in rice phytosterol biosynthesis using a customized sterol standards mixture. [Abstract]

2025 Nov;124(3):e70559. PMID: 41194406

Reinheit & Dokumentation

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Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (267 KB)
SDS (585 KB)
- English - EN (585 KB)
- Français - FR (585 KB)
- Deutsch - DE (585 KB)
- Norwegian - NO (585 KB)
- Español - ES (585 KB)
- Swedish - SV (585 KB)
- Italian - IT (585 KB)
- Korean - KR (585 KB)
- Portuguese - PT (585 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Cox, et al. The chemistry of extractives from hardwoods. Part XXVI. Experiments on cycloeucalenol, a new triterpene from Eucalyptus microcorys. Journal of the Chemical Society (Resumed), 1956. 1384–1392.

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

Cycloeucalenol

1 Cited Publications

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Cycloeucalenol

Publications Citing Use of MedChemExpress (MCE) Cycloeucalenol

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Chemical Information

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Cycloeucalenol Related Classifications

HY-N3666 Related Classifications