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Merck
CN

SMB01073

Eurycomanone

≥90% (LC/MS-ELSD)

Synonym(s):

Pasakbumin A

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About This Item

Empirical Formula (Hill Notation):
C20H24O9
CAS Number:
Molecular Weight:
408.40
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
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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

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Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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