20188-85-6 Usage
Description
Ombuoside is a flavonoid compound that exhibits antimicrobial properties, making it a potential candidate for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
Ombuoside is used as an antimicrobial agent for its ability to combat several strains of Gram-positive and Gram-negative bacteria, as well as the yeast Candida albicans. Its effectiveness against these microorganisms makes it a valuable asset in the development of new drugs and treatments for infections.
Used in Cosmetic Industry:
Ombuoside can be used as a natural preservative in cosmetic products due to its antimicrobial properties. This can help maintain the shelf life and safety of the products while reducing the need for synthetic preservatives.
Used in Food Industry:
In the food industry, Ombuoside can be utilized as a natural preservative to extend the shelf life of perishable items and inhibit the growth of harmful bacteria and fungi. This can contribute to improved food safety and quality.
Used in Agricultural Industry:
Ombuoside can be employed as a biopesticide or antimicrobial agent in agriculture to protect crops from bacterial and fungal infections. This can lead to increased crop yields and reduced reliance on chemical pesticides.
Overall, Ombuoside's antimicrobial activity makes it a versatile compound with potential applications across various industries, from pharmaceuticals to cosmetics, food, and agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 20188-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,8 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20188-85:
(7*2)+(6*0)+(5*1)+(4*8)+(3*8)+(2*8)+(1*5)=96
96 % 10 = 6
So 20188-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C29H34O16/c1-10-19(32)22(35)24(37)28(42-10)41-9-17-20(33)23(36)25(38)29(44-17)45-27-21(34)18-14(31)7-12(39-2)8-16(18)43-26(27)11-4-5-13(30)15(6-11)40-3/h4-8,10,17,19-20,22-25,28-33,35-38H,9H2,1-3H3/t10-,17+,19-,20+,22+,23-,24+,25+,28+,29-/m0/s1
20188-85-6Relevant articles and documents
Synthesized quercetin derivatives stimulate melanogenesis in B16 melanoma cells by influencing the expression of melanin biosynthesis proteins MITF and p38 MAPK
Yamauchi, Kosei,Mitsunaga, Tohru,Inagaki, Mizuho,Suzuki, Tohru
, p. 3331 - 3340 (2014/06/23)
In order to understand the effect of structure-activity relationships on melanogenesis using B16 melanoma cells, 19 quercetin derivatives were synthesized. Among the synthesized compounds, 3-O-methylquercetin (11) and 3′,4′,7-O-trimethylquercetin (14) increased melanin content more potently than the positive control theophylline, while exhibiting low cytotoxicity. Compound 11 exhibited less melanogenesis-stimulating activity than compound 14. However, 11 increased the expression of tyrosinase and tyrosinase-related protein 1 (TRP-1) to a greater extent than 14, thereby suggesting that melanogenesis in melanoma cells does not depend solely on the expression of the enzymes catalyzing melanin biosynthesis. Furthermore, 14 also stimulated the expression of the microphthalmia-associated transcription factor (MITF) and p-p38 mitogen activated protein kinase (MAPK), while they were not increased by 11. These results suggest that 11 may enhance the expression of tyrosinase and TRP-1 by regulating the proteasomal degradation of melanogenic enzymes and/or by activating other transcriptional factors regulating enzyme expression.
