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化驗
≥99.0% (HPLC)
mp
101-103 °C
101-104 °C (lit.)
溶解度
soluble 2.5%, clear, colorless (AcOH (MEOH))
SMILES 字串
CCCCCCCCOC(=O)c1cc(O)c(O)c(O)c1
InChI
1S/C15H22O5/c1-2-3-4-5-6-7-8-20-15(19)11-9-12(16)14(18)13(17)10-11/h9-10,16-18H,2-8H2,1H3
InChI 密鑰
NRPKURNSADTHLJ-UHFFFAOYSA-N
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一般說明
据报告，没食子酸辛酯（3，4，5-三羟基苯甲酸酯）对酿酒酵母和拜氏接合酵母具有抗真菌活性。与没食子酸辛酯相关的杀菌活性是由于其充当非离子表面活性剂（表面活性剂）的能力。据报告，没食子酸辛酯（一种没食子酸烷基酯）对金黄色葡萄球菌BB568具有直接的抗菌活性。据报告其可抑制大豆脂氧合酶-1（EC 1.13.11.12，I型）的活性，IC50为1.3 μM。对防止脂质过氧化也有效。
應用
在一项研究中，使用没食子酸辛酯研究了由没食子酸辛酯组成的两个梳状超分子系统中的自组装，该系统使用同步辐射将氢键合到聚异戊二烯-嵌段-聚（乙烯基吡啶）二嵌段共聚物的吡啶基上。
免責聲明
本品不可用作全球生物杀灭剂法规监管的生物杀灭剂，包括但不限于：美国联邦杀虫剂、杀菌剂和灭鼠剂法(US EPA′s Federal Insecticide Fungicide and Rodenticide Act)、欧盟生物杀灭剂法规(European Biocidal Products Regulation)、加拿大虫害管理监管机构(Canada’s Pest Management Regulatory Agency)、土耳其生物杀灭剂法规(Turkey’s Biocidal Products Regulation)、韩国生物杀灭剂法(Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR))等。
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Skin Sens. 1
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
Self-Assembly of Supramolecules Consisting of Octyl Gallate Hydrogen Bonded to Polyisoprene-b lock-poly (vinylpyridine) Diblock Copolymers.
Bondzic S, et al.
Macromolecules, 37(25), 9517-9524 (2004)
Tae Joung Ha et al.
Journal of agricultural and food chemistry, 52(10), 3177-3181 (2004-05-13)
Octyl gallate inhibited soybean lipoxygenase-1 (EC 1.13.11.12, type I) with an IC(50) of 1.3 microM. The inhibition of the enzyme by octyl gallate is a slow and reversible reaction without residual activity. The inhibition kinetics analyzed by Lineweaver-Burk plots indicates
Paul D Stapleton et al.
International journal of antimicrobial agents, 23(5), 462-467 (2004-05-04)
Aqueous extracts of Japanese green tea (Camellia sinensis) are able to reverse beta-lactam resistance in methicillin-resistant Staphylococcus aureus (MRSA). We have attributed the capacity to reverse oxacillin resistance in the homogeneous PBP2a producer BB568 and in EMRSA-16 to (-)-epicatechin gallate
Liisa Törmäkangas et al.
Biochemical pharmacology, 70(8), 1222-1230 (2005-09-06)
Increasing evidence suggests that plant polyphenolic compounds may protect from cardiovascular diseases, which have been addressed to their antioxidative properties. In addition, these compounds have been shown to possess anti-inflammatory and anti-microbial potential. In the present study we tested the
Anna Radomska
Acta poloniae pharmaceutica, 60(3), 191-195 (2003-10-15)
This paper reports on the effect of captopril on the stability of unsaturated fatty acids in the evening primrose oil. The experiment was performed for captopril at concentrations of 0.05%, 0.1% and 0.2% in the samples of evening primrose oil
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