17790
β-Eudesmol
≥90% (GC)
Synonyma:
(2R,4aR,8aS)-Decahydro-8-methylene-α,α,4a-trimethyl-2-naphthylmethanol
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Změnit zobrazení
| Velikost balení | Skladová položka | Dostupnost | Cena |
|---|---|---|---|
| 10 mg | Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti. | 8 000,00 Kč | |
| 50 mg | Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti. | 31 500,00 Kč |
O této položce
Empirický vzorec (Hillův zápis):
C15H26O
Číslo CAS:
Molekulová hmotnost:
222.37
UNSPSC Code:
12352212
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5735560
8 000,00 Kč
Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti.
Technický servis
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assay
≥90% (GC)
form
powder
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
2-8°C
SMILES string
[H][C@@]12C[C@@H](CC[C@@]1(C)CCCC2=C)C(C)(C)O
InChI
1S/C15H26O/c1-11-6-5-8-15(4)9-7-12(10-13(11)15)14(2,3)16/h12-13,16H,1,5-10H2,2-4H3/t12-,13+,15-/m1/s1
InChI key
BOPIMTNSYWYZOC-VNHYZAJKSA-N
General description
β-Eudesmol is an aromatic, oxygenated sesquiterpene compound.[1] It is primarily observed in the bark of mangolia trees and can also be extracted from other medical herbs such as Cryptomeria japonica, Atractylodes lancea, Pterocarpus santalinus, Ginkgo biloba, and Nardostachys jatamansi.
Application
β-Eudesmol has been used:
- as a treatment to test its antioxidant, anti-inflammatory, cell preservation effects on human dermal fibroblasts (HDFs)
- as a reference standard to investigate if metabolically engineered E. coli extracted terpene synthase (Tps) genes encode for β-eudesmol synthase by using gas chromatography-mass spectrometry (GC/MS) analysis[2]
- to test its antiviral effects against herpes simplex virus type 1 (HSV-1)[3]
- to test its reversal effects of cocaine-induced planarian behavior[1]
Biochem/physiol Actions
β-Eudesmol has many pharmacological benefits. It is an active ingredient present in many essential oils, showing antioxidant and antimicrobial activities. β-Eudesmol elicits its antifungal and anti-wood-decay fungal activities in leaf essential oil of Litsea coreana [4] tree, and the twigs of Taiwania cryptomerioides trees[5] respectively. It suppresses tumor cell proliferation, growth, and migration of human tumor cells.[6][7] β-Eudesmol is known to have various protective effects on the nervous system.[1]
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Tato položka | |||
|---|---|---|---|
| form powder | form crystals | form liquid | form powder |
| assay ≥90% (GC) | assay ≥99.0% (GC) | assay ≥95.0% (sum of enantiomers, GC) | assay >99% (TLC) |
| application(s) metabolomics | application(s) - | application(s) - | application(s) - |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level - |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. −20°C |
Skladovací třída
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty související s produkty, které jste v minulosti zakoupili, byly za účelem usnadnění shromážděny ve vaší Knihovně dokumentů.
Chen-Lung Ho et al.
Natural product communications, 5(10), 1677-1680 (2010-12-03)
The hydrodistilled leaf essential oil of Litsea coreana was analyzed by GC/FID and GC/MS. Fifty-two compounds were identified, the main components being n-decanal (27.5%), 2E,6E-farnesol (25.8%), beta-eudesmol (10.3%), ethyl n-dodecanoate (8.0%) and tau-cadinol (6.6%). Oxygenated sesquiterpenes (56.8%) and non-terpenoids (37.0%)
Jean Waikedre et al.
Chemistry & biodiversity, 9(3), 644-653 (2012-03-17)
Mortality due to fungal infections has increased substantially, becoming a worldwide problem in public health. As a contribution to the discovery of new antifungal agents, the properties of the heartwood essential oils of two trees growing in New Caledonia, Callitris
Antimicrobial and antioxidant activities and gas chromatography mass spectrometry (GC/MS) analysis of the essential oils of Ajuga bracteosa Wall. ex Benth. and Lavandula dentata L. growing wild in Yemen
Mothana RA, et al.,
Journal of Medicinal Plants Research, 6(15), 3066-3071 (2012)
Globální číslo obchodní položky
| Skladová položka | GTIN |
|---|---|
| 17790-10MG | 04061838753533 |
| 17790-50MG | 04061832404066 |