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                同义名:
                    
                        
                            2-羟基-6-十五基苯甲酸
                            
                             / Ginkgolic Acid C15:0; Hydroginkgolic acid
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Anacardic Acid是一种强效的p300和p300/CBP相关因子组蛋白乙酰转移酶抑制剂,此外还具有抗菌活性、抗微生物活性、前列腺素合成酶抑制作用、以及酪氨酸酶和脂氧合酶抑制作用。
 
                                 
                                
                            

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| 描述 | Anacardic acid is a potent inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases, which also has antibacterial activity, antimicrobial activity,prostaglandin synthase inhibition, and tyrosinase and lipoxygenase inhibition. | 
| Concentration | Treated Time | Description | References | |
| LNCaP cells | 0, 5, 25, 125 µM | 0, 4, 24, 48 hours | To investigate the effects of AA on LNCaP cell proliferation, it was found that AA significantly inhibited LNCaP cell proliferation, with the optimal concentration being 125 μmol/L and the optimal exposure time being 24 hours. | Chin J Cancer Res. 2012 Dec;24(4):275-83. | 
| A375 | 0.2 to 50 µM | 48 and 72 hours | To evaluate the cytotoxicity of Anacardic Acid on melanoma cell lines, results showed that Anacardic Acid significantly enhanced the cytotoxicity of liposomal Mitoxantrone. | Int J Nanomedicine. 2014 Jan 23;9:653-68. | 
| Hs294T | 0.2 to 50 µM | 48 and 72 hours | To evaluate the cytotoxicity of Anacardic Acid on melanoma cell lines, results showed that Anacardic Acid significantly enhanced the cytotoxicity of liposomal Mitoxantrone. | Int J Nanomedicine. 2014 Jan 23;9:653-68. | 
| NHDF | 0.2 to 50 µM | 48 and 72 hours | To evaluate the cytotoxicity of Anacardic Acid on normal cells, results showed that vitamin C had a protective effect on normal cells. | Int J Nanomedicine. 2014 Jan 23;9:653-68. | 
| MCF-7 | 1 nM – 100 µM | 48 hours | To evaluate the inhibitory effect of AnAc 24:1ω5 on the proliferation of MCF-7 cells | Mol Cancer Ther. 2010 Mar;9(3):594-605. | 
| LCC9 | 1 nM – 100 µM | 48 hours | To evaluate the inhibitory effect of AnAc 24:1ω5 on the proliferation of LCC9 cells | Mol Cancer Ther. 2010 Mar;9(3):594-605. | 
| LY2 | 1 nM – 100 µM | 48 hours | To evaluate the inhibitory effect of AnAc 24:1ω5 on the proliferation of LY2 cells | Mol Cancer Ther. 2010 Mar;9(3):594-605. | 
| MCF-10A | 1 nM – 100 µM | 48 hours | To evaluate the inhibitory effect of AnAc 24:1ω5 on the proliferation of MCF-10A cells | Mol Cancer Ther. 2010 Mar;9(3):594-605. | 
| MDA-MB-231 | 1 nM – 100 µM | 48 hours | To evaluate the inhibitory effect of AnAc 24:1ω5 on the proliferation of MDA-MB-231 cells | Mol Cancer Ther. 2010 Mar;9(3):594-605. | 
| Vero-E6 cells | 15 µM | 48 hours | To evaluate the antiviral potency of Anacardic Acid against SARS-CoV-2 in vitro, the results showed significant reduction in virus plaque formation at non-toxic concentrations. | Cell Biosci. 2021 Feb 28;11(1):45. | 
| Rat oligodendrocyte precursor cells (OPCs) | 10 µM | Anacardic acid induced the expression of myelin basic protein (MBP) and increased the expression of genes involved in the transcription of myelin proteins. | Proc Natl Acad Sci U S A. 2020 Sep 1;117(35):21527-21535. | |
| Rat oligodendrocyte precursor cells (OPCs) | 5.0 µM | Anacardic acid increased the mRNA expression of Mbp, Sp1, Sox10, and Purα. | Proc Natl Acad Sci U S A. 2020 Sep 1;117(35):21527-21535. | |
| Rat oligodendrocyte precursor cells (OPCs) | 2.5 µM | Anacardic acid increased the mRNA expression of IL-33. | Proc Natl Acad Sci U S A. 2020 Sep 1;117(35):21527-21535. | |
| Administration | Dosage | Frequency | Description | References | ||
| C57/B6 mice | Experimental allergic encephalitis (EAE) and cuprizone-induced demyelination model | 0.025 mg/kg to 2.5 mg/kg | Daily administration for 9 weeks | Anacardic acid improved pathological scores in EAE and cuprizone models and promoted remyelination. | Proc Natl Acad Sci U S A. 2020 Sep 1;117(35):21527-21535. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.87mL 0.57mL 0.29mL | 14.35mL 2.87mL 1.43mL | 28.69mL 5.74mL 2.87mL | |
| CAS号 | 16611-84-0 | 
| 分子式 | C22H36O3 | 
| 分子量 | 348.52 | 
| SMILES Code | O=C(O)C1=C(CCCCCCCCCCCCCCC)C=CC=C1O | 
| MDL No. | MFCD07368254 | 
| 别名 | 2-羟基-6-十五基苯甲酸 ;Ginkgolic Acid C15:0; Hydroginkgolic acid; 6-pentadecylsalicylic Acid | 
| 运输 | 蓝冰 | 
| InChI Key | ADFWQBGTDJIESE-UHFFFAOYSA-N | 
| Pubchem ID | 167551 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, 2-8°C | 
| 溶解方案 | DMSO: 105 mg/mL(301.27 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
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