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顺式-(+)-凯林内酯
Khellactone
|
产品编号 |
CFN96394 |
CAS编号 |
24144-61-4 |
分子式 = 分子量 |
C14H14O5 = 262.3 |
产品纯度 |
>=98% |
物理属性 |
Powder |
化合物类型 |
Coumarins |
植物来源 |
The roots of Angelica purpuraefolia. |
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 |
顺式-(+)-凯林内酯 |
CFN96394 |
24144-61-4 |
1mg |
QQ客服:3257982914 |
顺式-(+)-凯林内酯 |
CFN96394 |
24144-61-4 |
5mg |
QQ客服:3257982914 |
顺式-(+)-凯林内酯 |
CFN96394 |
24144-61-4 |
10mg |
QQ客服:3257982914 |
顺式-(+)-凯林内酯 |
CFN96394 |
24144-61-4 |
20mg |
QQ客服:3257982914 |
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ChemFaces的产品在许多优秀和顶级科学期刊中被引用
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Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914
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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
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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
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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
Monash University (Australia)
University of Zurich (Switzerland)
Johannes Gutenberg University Mainz (JGU) (Germany)
Universidad de La Salle (Mexico)
Universidad de Ciencias y Artes de Chiapas (Mexico)
VIB Department of Plant Systems Biology, UGent (PSB) (Belgium)
FORTH-IMBB (Greece)
Lodz University of Technology (Poland)
Michigan State University (USA)
University of Bordeaux (France)
MTT Agrifood Research Finland (Finland)
Pennsylvania State University (USA)
Sri Ramachandra University (India)
Universite Libre de Bruxelles (Belgium)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
J Cell Biochem.2018, 119(2):2231-2239
Appl. Sci.2023, 13(17), 9653.
Biomol Ther (Seoul).2020, 28(6):542-548.
Chem Biol Interact.2018, 290:44-51
Nutrients.2023, 15(6):1417.
Agronomy2020, 10(3),388.
J Ethnopharmacol.2023, 317:116789.
Translational Neuroscience2024, 15:20220339
Description: |
Khellactone shows antitumor activity,it can suppress the growth of NCI-H460 tumor cells. (+)-4'-cis-Khellactone and (+)-3'-cis-khellactone have antiplasmodial activities, they show notable inhibitory activity against -sensitive strains of with IC(50) values from 1.5 and 2.4 microM. |
Targets: |
Antifection |
In vitro: |
Phytother Res. 2010 Mar;24(3):469-71. | Antiplasmodial and cytotoxic activity of khellactone derivatives from Angelica purpuraefolia Chung.[Pubmed: 19960419 ] | The methanolic extract of the rhizomes parts of Agelica purpuraefolia was investigated for its activity against chloroquine-sensitive strains of Plasmodium falciparum using the parasite lactate dehydrogenase assay method.
METHODS AND RESULTS:
Two natural khellactone, (+)-4'-Decanoyl-cis-khellactone (1) and (+)-3'-Decanoyl-cis-khellactone (2) were isolated from the rhizomes parts of A. purpuraefolia. Two compounds were evaluated for in vitro antiplasmodial activities as well as their cytotoxic potential on SK-OV-3 cancer cell line cells. Compounds 1, 2 showed notable growth inhibitory activity against chloroquine-sensitive strains of Plasmodium falciparum with IC(50) values from 1.5 and 2.4 microM. This compound showed no significant cytotoxicity (IC(50) > 100 microM) evaluated using SK-OV-3 cancer cell line cells.
CONCLUSIONS:
This is the first report on the antiplasmodial activity of the compounds from A. purpuraefolia. |
|
In vivo: |
Phytother Res. 2007 May;21(5):406-9. | Isolation of coumarins and ferulate from the roots of Angelica purpuraefolia and the antitumor activity of khellactone.[Pubmed: 17236175 ] | A new coumarin, hydroxylomatin (1), was isolated from the CHCl(3)-soluble fraction of the roots of Angelica purpuraefolia, along with one ferulate (2) and three other known coumarins (3-5) including Khellactone (3). The structure of hydroxylomatin (1) was determined to be 3'beta,5'-dihydroxy-3',4'-dihydroseselin (1) by spectroscopic means including 2D-NMR. The modified Mosher's method was used to determine the chiral center at C-1 of compound 2. Khellactone (3) is a major compound of the roots of A. purpuraefolia.
METHODS AND RESULTS:
This study also examined the antitumor activity of Khellactone (3) using a LLC mouse lung carcinoma in the BDF-1 mice and a NCI-H460 human lung carcinoma in a human tumor xenograft model in nude mice. This compound (3) inhibited LLC tumor growth with a T/C (mean value of treated group/mean value of control group) value of 12.9% at a dose of 5 mg/kg and 33.2% at a dose of 10 mg/kg, respectively, in a dose-dependent manner. In addition, it suppressed the growth of NCI-H460 tumor cells, accounting for 81.4% at a dose of 10 mg/kg in nude mice. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
3.8124 mL |
19.0621 mL |
38.1243 mL |
76.2486 mL |
95.3107 mL |
5 mM |
0.7625 mL |
3.8124 mL |
7.6249 mL |
15.2497 mL |
19.0621 mL |
10 mM |
0.3812 mL |
1.9062 mL |
3.8124 mL |
7.6249 mL |
9.5311 mL |
50 mM |
0.0762 mL |
0.3812 mL |
0.7625 mL |
1.525 mL |
1.9062 mL |
100 mM |
0.0381 mL |
0.1906 mL |
0.3812 mL |
0.7625 mL |
0.9531 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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