
大果桉醛C
Macrocarpal C
|
产品编号 |
CFN99469 |
CAS编号 |
142628-53-3 |
分子式 = 分子量 |
C28H38O5 = 454.6 |
产品纯度 |
>=98% |
物理属性 |
Yellow powder |
化合物类型 |
Sesquiterpenoids |
植物来源 |
The branches of Eucalyptus globulus |
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 |
大果桉醛C |
CFN99469 |
142628-53-3 |
1mg |
QQ客服:2056216494 |
大果桉醛C |
CFN99469 |
142628-53-3 |
5mg |
QQ客服:2056216494 |
大果桉醛C |
CFN99469 |
142628-53-3 |
10mg |
QQ客服:2056216494 |
大果桉醛C |
CFN99469 |
142628-53-3 |
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
Johannes Gutenberg University Mainz (JGU) (Germany)
Wageningen University (Netherlands)
Gyeongsang National University (Korea)
University of East Anglia (United Kingdom)
Universita' Degli Studi Di Cagliari (Italy)
The University of Newcastle (Australia)
University of Cincinnati (USA)
Mahidol University (Thailand)
Pennsylvania State University (USA)
University of Illinois at Chicago (USA)
Melbourne University (Australia)
Siksha O Anusandhan University (India)
Biotech R&D Institute (USA)
Vin?a Institute of Nuclear Sciences (Serbia)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
Biomolecules.2019, 9(11):E696
GENENCELL2023, 25:4356740
Plant Physiol Biochem.2019, 144:355-364
ACS Omega2020, 5,33,20825-20830
Appl. Sci.2020, 10(23), 8729
Antioxidants (Basel).2022, 11(12):2411.
JEJU National University2022, 24032.
J Microbiol Biotechnol.2023, 33(10):1317-1328.
Description: |
Macrocarpal C, isolated from the fresh leaves of Eucalyptus globulus Labill. (Lan An) and identified as its major antifungal component by bioassay-guided purification, the antifungal action of macrocarpal C was associated with increases of membrane permeability, intracellular ROS and DNA fragmentation. |
Targets: |
ROS | Antifection |
In vitro: |
Am J Chin Med. 2010;38(5):1005-14. | Two antifungal components isolated from Fructus Psoraleae and Folium Eucalypti Globuli by bioassay-guided purification.[Pubmed: 20821830] | Fructus Psoraleae and Folium Eucalypti Globuli have long been used as Chinese medicines to treat various ailments such as asthma, eczema and dermatomycosis. In previous studies, their antifungal activities were demonstrated. The aim of the present study was to isolate active antidermatophytic compounds from their ethanolic extracts by means of bioassay-guided purification.
METHODS AND RESULTS:
Guided by the inhibitory activities on Trichophyton mentagrophytes, Trichophyton rubrum and Paecilomyces variotii, bakuchiol was isolated from the n-hexane fraction of Fructus Psoraleae whilst Macrocarpal C was isolated from the n-hexane fraction of Folium Eucalypti Globuli. Both pure compounds could effectively inhibit the growth of dermatophytes in vitro.
CONCLUSIONS:
This is the first paper to report the isolation and identification of active antidermatophytic compounds from Fructus Psoraleae and Folium Eucalypti Globuli by the bioassay-guided purification. | Chin Med. 2015 Nov 21;10:34. | Antifungal mode of action of macrocarpal C extracted from Eucalyptus globulus Labill (Lan An) towards the dermatophyte Trichophyton mentagrophytes.[Pubmed: 26594235 ] | The fresh leaves of Eucalyptus globulus Labill. (Lan An) have been used in Chinese medicine for many years to treat dermatomycosis. Macrocarpal C was isolated from this herb and identified as its major antifungal component by bioassay-guided purification.
This study aims to investigate the antifungal activity of Macrocarpal C against Trichophyton mentagrophytes, which can cause tinea pedis. METHODS AND RESULTS: The suppression in the growth of T. mentagrophytes following its treatment with Macrocarpal C was associated with an increase in the permeability of the fungal membrane (P = 0.0043 when compared to control); an increase in the production of intracellular ROS (P = 0.0063); and the induction of apoptosis as a consequence of DNA fragmentation (P = 0.0007). CONCLUSION:
CONCLUSIONS:
This study demonstrated that the antifungal action of Macrocarpal C was associated with increases of membrane permeability, intracellular ROS and DNA fragmentation. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
2.1997 mL |
10.9987 mL |
21.9974 mL |
43.9947 mL |
54.9934 mL |
5 mM |
0.4399 mL |
2.1997 mL |
4.3995 mL |
8.7989 mL |
10.9987 mL |
10 mM |
0.22 mL |
1.0999 mL |
2.1997 mL |
4.3995 mL |
5.4993 mL |
50 mM |
0.044 mL |
0.22 mL |
0.4399 mL |
0.8799 mL |
1.0999 mL |
100 mM |
0.022 mL |
0.11 mL |
0.22 mL |
0.4399 mL |
0.5499 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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