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经验公式(希尔记法):
C20H24O9
化学文摘社编号:
分子量:
408.40
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
408.4
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
SMILES string
O1[C@@]2([C@H]3[C@]4([C@H](OC(=O)[C@@H]([C@]4(C(=C)[C@H]2O)O)O)C[C@@H]5[C@@]3([C@@H](C(=O)C=C5C)O)C)C1)O
InChI
1S/C20H24O9/c1-7-4-10(21)13(23)17(3)9(7)5-11-18-6-28-20(27,16(17)18)12(22)8(2)19(18,26)14(24)15(25)29-11/h4,9,11-14,16,22-24,26-27H,2,5-6H2,1,3H3/t9-,11+,12+,13+,14-,16+,17+,18+,19-,20-/m0/s1
InChI key
UCUWZJWAQQRCOR-OKNZMGBLSA-N
General description
Eurycomanone, also known as Pasakbumin A, is a bioactive quassinoid natural compound commonly derived from Eurycoma longifolia (Tongkat Ali). Current research indicates that this plant metabolite is an inhibitor and may possess diverse biological activities, including antitumor, antimalarial, and anticancer properties.
Application
Eurycomanone is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
Biochem/physiol Actions
Eurycomanone inhibited Jurkat and K562 leukemia cells viability and proliferation without affecting healthy cells and enhanced testosterone steroidogenesis.
Features and Benefits
- Suitable for Biochemical and Biomedical research
- Versatile and adaptable for wide variety of laboratory and research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
