
曲酸
Kojic acid
|
|
产品编号 |
CFN94478 |
| CAS编号 |
501-30-4 |
| 分子式 = 分子量 |
C6H6O4 = 142.11 |
| 产品纯度 |
>=98% |
| 物理属性 |
Powder |
| 化合物类型 |
Miscellaneous |
| 植物来源 |
From the Aspergillus parasiticus. |
| 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 |
| 曲酸 |
CFN94478 |
501-30-4 |
10mg |
QQ客服:3257982914 |
| 曲酸 |
CFN94478 |
501-30-4 |
20mg |
QQ客服:3257982914 |
| 曲酸 |
CFN94478 |
501-30-4 |
50mg |
QQ客服:3257982914 |
| 曲酸 |
CFN94478 |
501-30-4 |
100mg |
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

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
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Leibniz Institute of Plant Biochemistry (Germany)
Agricultural Research Organization (ARO) (Israel)
Kitasato University (Japan)
Univerzita Karlova v Praze (Czech Republic)
Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
Universiti Kebangsaan Malaysia (Malaysia)
Helmholtz Zentrum München (Germany)
Research Unit Molecular Epigenetics (MEG) (Germany)
Julius Kühn-Institut (Germany)
University of the Basque Country (Spain)
Universitas islam negeri Jakarta (Indonesia)
University of Beira Interior (Portugal)
Shanghai Institute of Biochemistry and Cell Biology (China)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
| Description: |
Kojic acid has been used as a food additive for preventing enzymatic browning of crustaceans and as a cosmetic agent for skin whitening.
Kojic acid exhibits concentration-dependent scavenging activity on DPPH possessing strong antioxidant activity, it can reduce the mortality induced by gamma irradiation; it exhibits a competitive inhibition for the oxidation of chlorogenic acid and catechol by potato polyphenol oxidase (PPO) and of 4-methylcatechol and chlorogenic acid by apple PPO; it also has significant tyrosinase inhibitory activity.
|
| Targets: |
Tyrosinase |
| In vitro: |
| J Pharm Pharmacol. 1994 Dec;46(12):982-5. | | Kojic acid, a cosmetic skin whitening agent, is a slow-binding inhibitor of catecholase activity of tyrosinase.[Pubmed: 7714722] | METHODS AND RESULTS:
It was found that kojic acid, which is used in cosmetics for its excellent whitening effect, inhibits catecholase activity of tyrosinase in a non-classical manner. A decrease in the initial velocity to a steady-state inhibited velocity can be observed over a few minutes. This time-dependence, which is unaltered by prior incubation of the enzyme with the inhibitor, is consistent with a first-order transition.
CONCLUSIONS:
The kinetic data obtained correspond to those for a postulated mechanism that involves the rapid formation of an enzyme inhibitor complex that subsequently undergoes a relatively slow reversible reaction. Kinetic parameters characterizing this type of inhibition were evaluated by means of nonlinear regression of product accumulation curves. |
|
| In vivo: |
| Toxicol Sci. 2004 Sep;81(1):43-9. | | Enhancement of hepatocarcinogenesis by kojic acid in rat two-stage models after initiation with N-bis(2-hydroxypropyl)nitrosamine or N-diethylnitrosamine.[Pubmed: 15201437] |
Kojic acid (KA) has been used as a food additive for preventing enzymatic browning of crustaceans and as a cosmetic agent for skin whitening. METHODS AND RESULTS: In the present experiments, effects of KA on the induction of hepatic pre-neoplastic lesions in N-bis(2-hydroxypropyl)nitrosamine-initiated (experiment 1) and non-initiated (experiment 2) models, and its promoting influence in a medium-term liver bioassay (experiment 3) were investigated at dietary doses of up to 2% in male F344 rats. In experiment 1, 2% KA feeding induced significant increases in numbers (22.3 +/- 13.0 vs 8.5 +/- 3.4 in the 0%) and areas (0.37 +/- 0.29 vs 0.05 +/- 0.03 in the 0%) of glutathione-S-transferase P form (GST-P)-positive foci and toxic changes such as vacuolation of hepatocytes and microgranulomas. The development of GST-P-positive foci was pronounced in the animals with hepatocellular toxic changes. In experiment 2, numbers (0.65 +/- 0.57 vs 0.17 +/- 0.28 in the 0%) and areas (0.005 +/- 0.005 vs 0.0007 +/- 0.0012 in the 0%) of GST-P-positive foci and hepatocellular proliferating cell nuclear antigen (PCNA) expression (3.8 +/- 2.3 vs 2.6 +/- 0.7 in the 0%) were significantly increased by the 2% treatment. The PCNA-positive hepatocytes were abundantly localized around the vacuolated and granulomatous legions in both experiments 1 and 2. In experiment 3, significant increases in numbers (16.9 +/- 3.2 vs 8.4 +/- 2.7 in the 0%) and areas (1.62 +/- 0.39 vs 0.77 +/- 0.34 in the 0%) of GST-P-positive foci were again observed with 2% KA. CONCLUSIONS: These results demonstrate tumor-promoting and possible hepatocarcinogenic activity of KA at 2%, but the carcinogenic potential is likely to be weak. This study also indicated that enhanced replication of hepatocytes related to toxic changes might be involved as an underlying mechanism. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
| 1 mM |
7.0368 mL |
35.184 mL |
70.368 mL |
140.736 mL |
175.9201 mL |
| 5 mM |
1.4074 mL |
7.0368 mL |
14.0736 mL |
28.1472 mL |
35.184 mL |
| 10 mM |
0.7037 mL |
3.5184 mL |
7.0368 mL |
14.0736 mL |
17.592 mL |
| 50 mM |
0.1407 mL |
0.7037 mL |
1.4074 mL |
2.8147 mL |
3.5184 mL |
| 100 mM |
0.0704 mL |
0.3518 mL |
0.7037 mL |
1.4074 mL |
1.7592 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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