
紫黄檀素
Violanone
|
|
产品编号 |
CFN95385 |
| CAS编号 |
52250-38-1 |
| 分子式 = 分子量 |
C17H16O6 = 316.3 |
| 产品纯度 |
>=98% |
| 物理属性 |
Powder |
| 化合物类型 |
Flavonoids |
| 植物来源 |
The roots of Parochetus communis |
| ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用 |
|
| 产品名称 |
产品编号 |
CAS编号 |
包装 |
QQ客服 |
| 紫黄檀素 |
CFN95385 |
52250-38-1 |
1mg |
QQ客服:2056216494 |
| 紫黄檀素 |
CFN95385 |
52250-38-1 |
5mg |
QQ客服:2056216494 |
| 紫黄檀素 |
CFN95385 |
52250-38-1 |
10mg |
QQ客服:2056216494 |
| 紫黄檀素 |
CFN95385 |
52250-38-1 |
20mg |
QQ客服:2056216494 |
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ChemFaces的产品在许多优秀和顶级科学期刊中被引用

Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.
IF=13.297(2019)PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)PMID: 30417089
我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
Institute of Tropical Disease Universitas Airlangga (Indonesia)
Universidad de Antioquia (Colombia)
Centralised Purchases Unit (CPU), B.I.T.S (India)
Uniwersytet Medyczny w ?odzi (Poland)
Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
Lund University (Sweden)
Shanghai University of TCM (China)
University of Toronto (Canada)
Universidad de La Salle (Mexico)
University of Pretoria (South Africa)
University of Canterbury (New Zealand)
Harvard University (USA)
Aveiro University (Portugal)
Kyung Hee University (Korea)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
| Description: |
Violanone, an isoflavanone compound, can inhibit tubulin polymerization. Violanone also exhibits larvicidal activity against A. aegypti. |
| In vitro: |
| Exp Parasitol . 2015 Jun;153:160-164. | | Extract of Bowdichia virgilioides and maackiain as larvicidal agent against Aedes aegypti mosquito[Pubmed: 25819294] | | The larvicidal activities of extracts of three hardwood species (Hymenaea stigonorcapa, Anadenanthera colubrina and Bowdichia virgilioides) against 4th instar larvae of Aedes aegypti were evaluated using WHO guidelines. Extracts of H. stignocarpa and A. colubrina showed weak activity. The highest larvicidal effect was obtained with the cyclohexane extract of the heartwood of B. virgilioides, which caused 100% mortality at concentrations at 50 and 100 μg/mL. Fraction toluene/EtOAc (8:2) from this extract showed larvicidal activity (LC₅₀ = 34.90 ± 1.27 μg/mL). A mixture of two compounds identified as medicarpin and maackiain exhibited a very good larvicidal activity (sub-fraction 2, LC₅₀ = 17.5 ± 1.87 μg/mL) and maackiain showed to be a strong larvicidal compound (LC₅₀ = 21.95 ± 1.34 μg/mL). This result can be of value in the search for new natural larvicidal compounds from other hardwood plant extracts and presents the first report of B. virgilioides being used to control a mosquito vector. | | Tetrahedron. 2007 Dec 24; 63(52): 12986-12993. | | Synthesis and biological evaluation of isoflavone analogues from Dalbergia oliveri[Reference: WebLink] | | Mucronulatol 1 and violanone 2 isolated from Dalbergia oliveri Gamble, and the corresponding isoflavone 3 were prepared by ligand coupling reactions involving organolead reagent. Biological studies have shown a significant cytotoxic effect against an HBL100 leukemia cell line only for isoflavan 1 with an IC50 value amounting to 5.7 μM. All the drugs modestly inhibit the in vitro microtubule assembly, independently of the cytotoxic ability. Natural compounds 1 and 2 have no antibacterial activity, but are potent inhibitors of the Fusarium oxysporum phytopathogenic fungal growth. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
| 1 mM |
3.1616 mL |
15.8078 mL |
31.6156 mL |
63.2311 mL |
79.0389 mL |
| 5 mM |
0.6323 mL |
3.1616 mL |
6.3231 mL |
12.6462 mL |
15.8078 mL |
| 10 mM |
0.3162 mL |
1.5808 mL |
3.1616 mL |
6.3231 mL |
7.9039 mL |
| 50 mM |
0.0632 mL |
0.3162 mL |
0.6323 mL |
1.2646 mL |
1.5808 mL |
| 100 mM |
0.0316 mL |
0.1581 mL |
0.3162 mL |
0.6323 mL |
0.7904 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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