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关于此项目
经验公式(希尔记法):
C25H24O12
化学文摘社编号:
分子量:
516.45
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352205
MDL number:
InChI
1S/C25H24O12/c26-15-5-1-13(9-17(15)28)3-7-21(31)36-20-12-25(35,24(33)34)11-19(30)23(20)37-22(32)8-4-14-2-6-16(27)18(29)10-14/h1-10,19-20,23,26-30,35H,11-12H2,(H,33,34)/b7-3+,8-4+/t19-,20-,23+,25-/m1/s1
SMILES string
O[C@@H]1C[C@@](O)(C[C@@H](OC(=O)\C=C\c2ccc(O)c(O)c2)[C@H]1OC(=O)\C=C\c3ccc(O)c(O)c3)C(O)=O
InChI key
UFCLZKMFXSILNL-RVXRWRFUSA-N
Quality Level
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
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General description
4,5-Di-O-咖啡酰奎宁酸(4,5-COQ)作为咖啡酰奎宁酸的衍生物,是一种具有生物活性的苯丙素。
Application
4,5-Di-O-咖啡酰奎宁酸可作为参考标准物,利用高效液相色谱和二极管阵列检测(HPLC-DAD)检测蒿属植物中的酚类化合物还可分别作为高效液相色谱和二极管阵列检测(HPCL-DAD)的标准物。
Biochem/physiol Actions
4,5-Di-O-咖啡酰奎宁酸(4,5-COQ)是一种优异的抗氧化剂、抗炎剂、抗菌剂、抗真菌剂和细胞保护剂。此外,它还表现出神经保护和抗淀粉样变等特性,并能够抑制 42-聚淀粉样β-蛋白(Aβ42)。4,5-COQ 具有抗人类免疫缺陷病毒(HIV)活性,因其能有效抑制 HIV-1 逆转录酶。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Phenolic compounds and in vitro antioxidant, anti-inflammatory, antimicrobial activities of Scorzonera hieraciifolia Hayek roots
Sari A, et al.,
Asia-Pacific Journal of Molecular Biology and Biotechnology, 125, 116-119 (2019)
HIV-1 reverse transcriptase inhibitory activity of flavones and chlorogenic acid derivatives from Moquiniastrum floribundum (Asteraceae)
Tamayose CI, et al.,
South African Journal of botony, 123, 142-146 (2019)
HIV-1 reverse transcriptase inhibitory activity of flavones and chlorogenic acid derivatives from Moquiniastrum floribundum (Asteraceae)
Tamayose CI, et al.,
Asia-Pacific Journal of Molecular Biology and Biotechnology, 123, 142-146 (2019)
Phenolic compounds and in vitro antioxidant, anti-inflammatory, antimicrobial activities of Scorzonera hieraciifolia Hayek roots
Sari A, et al.,
South African Journal of botony, 125, 116-119 (2019)
Yinku Liang et al.
Molecular medicine reports, 21(1), 229-239 (2019-11-21)
In this study, six compounds were isolated and purified from dandelion, and only sample I exhibited notable antifungal effect on Candida albicans (CA). high‑performance liquid chromatography‑diode‑array detector‑electrospray ionization‑tandem mass spectrometry analysis showed that sample I comprised 4‑coumaric acid, ferulic acid, quercetin
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