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和厚樸酚
分析標(biāo)準(zhǔn)品,HPLC≥98%
Honokiol
CAS號(hào)：35354-74-6
分子式：C18H18O2
分子量：266.33
MDL：MFCD00016674
貨號(hào) | 規(guī)格/參數(shù)/品牌 | 價(jià)格 | 貨期 |
YJ-B20498-20mg | 分析標(biāo)準(zhǔn)品,HPLC≥98% | ￥180.00 | 現(xiàn)貨 |
JS31381-1g | 98% | ￥520.00 | 現(xiàn)貨 |
JS31381-5g | 98% | ￥1280.00 | 現(xiàn)貨 |
JS31381-25g | 98% | ￥2980.00 | 現(xiàn)貨 |
A10304-20mg | 分析標(biāo)準(zhǔn)品,含量98.7%，可溯源 | ￥270.00 | 現(xiàn)貨 |
YJ-BW10003-50mg | 分析標(biāo)準(zhǔn)品,標(biāo)準(zhǔn)物質(zhì)，見(jiàn)證書(shū) | ￥294.00 | 現(xiàn)貨 |
產(chǎn)品介紹
熔點(diǎn)：87.5℃
沸點(diǎn)：400.1℃ at 760 mmHg
外觀：棕褐色至白色精細(xì)粉末，單體為無(wú)色鱗片狀晶體
溶解性：可溶于一般的有機(jī)溶劑，易溶于苯，乙mi，氯仿，乙醇等，難溶于水。
儲(chǔ)存條件：2-8℃
注意：部分產(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。
參考文獻(xiàn)(39篇)
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38. [IF=1.7] Yu-Han Piao et al."Integrating Intestinal Biotransformation and Gut Microbiota to Uncover the Influence of Tongfu Xiexia Decoction in Rats With Constipation."RAPID COMMUNICATIONS IN MASS SPECTROMETRY.2025 May;39(15):e10065
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34. [IF=4.8] Haitao Li et al."Honokiol relieves hippocampal neuronal damage in Alzheimer's disease by activating the SIRT3‐mediated mitochondrial autophagy."CNS Neuroscience & Therapeutics.2024 Aug; 30(8): e14878
33. [IF=8.2] Yulong Wei et al."New insight into molecular mechanisms of different polyphenols affecting Sirtuin 3 deacetylation activity."INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES".2024 May;:132026
32. [IF=3] Xiaoshuang He et al."Affinity character analysis of magnolol and honokiol based on stepwise frontal analysis coupled with cell membrane chromatography."JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES.2023 Sep;1229:12
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29. [IF=2.866] Sun, Guang-wei et al."Honokiol Reduces Mitochondrial Dysfunction and Inhibits Apoptosis of Nerve Cells in Rats with Traumatic Brain Injury by Activating the Mitochondrial Unfolded Protein Response."JOURNAL OF MOLECULAR NEUROSCIENCE.2022 Dec;:1-9
28. [IF=3.251] Kanglei Zhang et al."Honokiol Antagonizes Cadmium-Induced Nephrotoxicity in Quail by Alleviating Autophagy Dysfunction, Apoptosis and Mitochondrial UPR Inhibition with Its Antioxidant Properties."Life-Basel.2022 Oct;12(10):1574
27. [IF=11.467] Xinmian Chen et al."Local delivery of gambogic acid to improve anti-tumor immunity against oral squamous cell carcinoma."JOURNAL OF CONTROLLED RELEASE.2022 Nov;351:381
26. [IF=4.927] Wenguang Jing et al."Application of Multiple-Source Data Fusion for the Discrimination of Two Botanical Origins of Magnolia Officinalis Cortex Based on E-Nose Measurements, E-Tongue Measurements, and Chemical Analysis."MOLECULES.2022 Jan;27(12):3892
25. [IF=3.373] Kewei Zhang et al."Discrimination between raw and ginger juice processed Magnoliae officinalis cortex based on HPLC and Heracles NEO ultra-fast gas phase electronic nose."Phytochemical Analysis. 2022 Mar 22
24. [IF=1.719] Xiaoying Zhu et al."Honokiol suppresses TNF-α-induced migration and matrix metalloproteinase expression by blocking NF-κB activation via the ERK signaling pathway in rat aortic smooth muscle cells."Acta Histochem. 2014 May;116:588
23. [IF=1.902] Junjun Wang et al."The pharmacokinetics and tissue distribution of curcumin and its metabolites in mice."Biomed Chromatogr. 2018 Sep;32(9):e4267
22. [IF=2.939] Fan Shuli et al."Honokiol Inhibits Tumor Necrosis Factor-α-Stimulated Rat Aortic Smooth Muscle Cell Proliferation via Caspase- and Mitochondrial-Dependent Apoptosis."Inflammation. 2014 Feb;37(1):17-26
21. [IF=3.205] Dong-Dong Hu et al."Simultaneous determination of ten compounds in rat plasma by UPLC-MS/MS: Application in the pharmacokinetic study of Ma-Zi-Ren-Wan."J Chromatogr B. 2015 Sep;1000:136
20. [IF=5.418] Qiu Ling et al."Honokiol ameliorates endothelial dysfunction through suppression of PTX3 expression, a key mediator of IKK/IκB/NF-κB, in atherosclerotic cell model."Exp Mol Med. 2015 Jul;47(7):e171-e171
19. [IF=5.81] Zhang Xianhua et al."Pharmacokinetic Study of 7 Compounds Following Oral Administration of Fructus Aurantii to Depressive Rats."Front Pharmacol. 2018 Mar;0:131
18. Qiu, Ling, et al. "Honokiol ameliorates endothelial dysfunction through suppression of PTX3 expression, a key mediator of IKK/IκB/NF-κB, in atherosclerotic cell model." Experimental & molecular medicine 47.7 (2015): e171-e171.
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