SMB00110
Plumieride
≥95% (LC/MS-ELSD)
Synonym(s):
Agoniadin
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assay
≥95% (LC/MS-ELSD)
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
SMILES string
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3[C@@H]1C=C[C@]34OC(=O)C(=C4)[C@H](C)O
InChI
1S/C21H26O12/c1-8(23)10-5-21(33-18(10)28)4-3-9-11(17(27)29-2)7-30-19(13(9)21)32-20-16(26)15(25)14(24)12(6-22)31-20/h3-5,7-9,12-16,19-20,22-26H,6H2,1-2H3/t8-,9+,12+,13+,14+,15-,16+,19-,20-,21+/m0/s1
InChI key
AOPMSFXOYJXDNJ-IRFSQMTFSA-N
General description
Natural product derived from plant source.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Sebastião de O Rebouças et al.
Journal of ethnopharmacology, 147(2), 474-480 (2013-03-27)
Himatanthus articulatus (Apocynaceae) is a plant native to the Amazon, popularly used to treat external ulcers, tumors, inflammations, cancer, syphilis and malaria. To investigate the in vivo genotoxic and mutagenic potential of this plant, using the comet assay and the
Mahabeer P Dobhal et al.
The Journal of organic chemistry, 69(19), 6165-6172 (2004-09-11)
Plumieride was isolated as one of the major components from the biologically active methanolic extract of the bark of Plumeria bicolor (family Apocynaceae). For investigating the effect of substituents on cytotoxic activity it was modified into a series of compounds.
M S Abdel-Kader et al.
Journal of natural products, 60(12), 1294-1297 (1998-01-15)
Bioassay-guided fractionation of the EtOAc extract of both Allamanda cathartica and Himatanthus fallax (Apocynaceae) using the Sc-7 yeast strain resulted in the isolation of the weakly cytotoxic isoplumericin and plumericin. In addition, the new lignan 7(R)-methoxy-8-epi-matairesional and three known compounds
Global Trade Item Number
| SKU | GTIN |
|---|---|
| SMB00110-1MG | 04061826168516 |