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10Z-Nonadecenoic acid Sale

(Synonyms: 十九碳烯酸(顺-10)) 目录号 : GC33800

10Z-Nonadecenoic acid 是一种具有抗肿瘤活性的长链脂肪酸。也可以抑制 p53 活性

10Z-Nonadecenoic acid Chemical Structure

Cas No.:73033-09-7

规格 价格 库存 购买数量
10mg
¥714.00
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产品描述

cis-10-Nonadecenoic acid is a C19:1 monounsaturated fatty acid. It has been examined for potential antitumor activity and was reported to inhibit HL-60 cell proliferation with an IC50 value of 295 ?M and to prevent LPS-induced tumor necrosis factor production from mouse macrophages.1 Furthermore, long-chain fatty acids, such as cis-10-nonadecenoic acid, have been shown to inhibit p53 activity.2

1.Fukuzawa, M., Yamaguchi, R., Hide, I., et al.Possible involvement of long chain fatty acids in the spores of Ganoderma lucidum (Reishi Houshi) to its anti-tumor activityBiol. Pharm. Bull.31(10)1933-1937(2008) 2.Iijima, H., Kasai, N., Chiku, H., et al.The inhibitory action of long-chain fatty acids on the DNA binding activity of p53Lipids41(6)521-527(2006)

Chemical Properties

Cas No. 73033-09-7 SDF
别名 十九碳烯酸(顺-10)
Canonical SMILES CCCCCCCC/C=C\CCCCCCCCC(O)=O
分子式 C19H36O2 分子量 296.49
溶解度 DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 30 mg/ml,Ethanol:PBS (pH7.2) (1:7): 0.25 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 3.3728 mL 16.864 mL 33.728 mL
5 mM 0.6746 mL 3.3728 mL 6.7456 mL
10 mM 0.3373 mL 1.6864 mL 3.3728 mL
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Research Update

Analysis of gut microbiota and metabolites in patients with rheumatoid arthritis and identification of potential biomarkers

Aging (Albany NY) 2021 Oct 20;13(20):23689-23701.PMID:34670873DOI:PMC8580343

Rheumatoid arthritis (RA) is an autoimmune disease described by joint destruction, synovitis and pannus formation. The gut microbiota acts as an environmental factor that plays an important role in RA, but little research regarding the etiopathogenic mechanisms of the microbiome in RA has been carried out. We used an integrated approach of 16S rRNA gene sequencing and ultrahigh-performance liquid chromatography-mass spectrometry-based metabolomics to analyze the structure and diversity of the intestinal flora and metabolites of the gut microbiota in RA patients compared with healthy subjects. In this study, α-diversity analysis of the gut microbiota showed that there was no significant difference between the healthy control (HC) and RA groups. However, β-diversity analysis showed that there was a significant difference between the two groups. Further analysis of alteration of the gut microbiota revealed that at the phylum level, the relative abundance of p_Bacteroidetes was significantly decreased in the RA group, while that of Verrucomicrobia and Proteobacteria was significantly increased in the RA group. At the genus level, Bacteroides, Faecalibacterium and some probiotics were decreased in the RA group, while 97 genera, including Lactobacillus, Streptococcus and Akkermansia, were increased in the RA group. Seventy-four differentially abundant metabolites were identified between the HC and RA groups, and we identified two potential biomarkers (9,12-octadecadiynoic acid and 10Z-Nonadecenoic acid) in RA.