82415
Prunetin
≥98.0% (TLC)
Synonym(s):
4′,5-Dihydroxy-7-methoxyisoflavone
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5 MG
PLN 509.00
25 MG
PLN 2,060.00
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5 MG
PLN 509.00
25 MG
PLN 2,060.00
About This Item
Empirical Formula (Hill Notation):
C16H12O5
CAS Number:
Molecular Weight:
284.26
Beilstein:
292155
EC Number:
MDL number:
UNSPSC Code:
51111800
PubChem Substance ID:
NACRES:
NA.77
Recommended Products
Assay
≥98.0% (TLC)
form
powder
SMILES string
COc1cc(O)c2C(=O)C(=COc2c1)c3ccc(O)cc3
InChI
1S/C16H12O5/c1-20-11-6-13(18)15-14(7-11)21-8-12(16(15)19)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3
InChI key
KQMVAGISDHMXJJ-UHFFFAOYSA-N
Biochem/physiol Actions
Inhibitor of both cytoplasmic and mitochondrial human liver aldehyde dehydrogenases, possibly by binding at an allosteric site.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Bumjung Kim et al.
Molecules (Basel, Switzerland), 23(9) (2018-09-20)
Prunetin, a component of herbal medicines and various foods, such as pea, peach, cherry, and Prunus yedoensis, is a useful pharmacological compound. We previously reported the potent vasorelaxant effect of the bark of P. yedoensis. Therefore, we investigated the vasorelaxant
Preethi Vetrivel et al.
Biomolecules, 10(7) (2020-07-28)
Gastric cancer is the common type of malignancy positioned at second in mortality rate causing burden worldwide with increasing treatment options. Prunetin (PRU) is an O-methylated flavonoid that belongs to the group of isoflavone executing beneficial activities. In the present
Su-Ling Wong et al.
Journal of natural products, 74(12), 2489-2496 (2011-12-14)
Bioassay-guided fractionation of the roots of Neolitsea daibuensis afforded three new β-carboline alkaloids, daibucarbolines A-C (1-3), three new sesquiterpenoids, daibulactones A and B (4 and 5) and daibuoxide (6), and 20 known compounds. The structures of 1-6 were determined by
Y Yura et al.
Archives of virology, 132(3-4), 451-461 (1993-01-01)
Genistein, an inhibitor of protein-tyrosine kinase, inhibited the replication of herpes simplex virus type 1 (HSV-1) at genistein concentrations of more than 25 microM, whereas the related compounds, which do not inhibit protein-tyrosine kinases, did not affect the replication of
Takeki Tsutsui et al.
International journal of cancer, 105(3), 312-320 (2003-04-22)
For the simultaneous assessment of in vitro carcinogenicity and mutagenicity of phytoestrogens, the abilities of 5 phytoestrogens, daidzein, genistein, biochanin A, prunetin, and coumestrol, to induce cell transformation and genetic effects were examined using the Syrian hamster embryo (SHE) cell
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