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三桠苦属

  • 3,5,6-trihydroxysitostane
    T84308133697-68-4In house
    3,5,6-trihydroxysitostane 是一种从吴茱萸果实中提取的类固醇天然产物。
    • ¥ 1300
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  • Stigmastane-3,5,6-triol
    TN506720835-91-0
    Stigmastane-3,5,6-triol and derivatives could be used for preparing antiviral medicine.
    • ¥ 2760
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  • Evodosin A
    TN40441291053-38-7
    Evodosin A 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4044,CAS号为 1291053-38-7。
    • ¥ 3940
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  • Evodine
    TCS23366989-38-4
    Evodine 是吴茱萸中的主要柠檬苦素,是P-gp 有效抑制剂,可通过保留抗氧化剂防御系统,针对谷氨酸诱导的毒性具有保护作用。
    • ¥ 478
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  • 1-Methyl-2-[(Z)-6-undecenyl]-4(1H)-quinolone
    TN6057120693-49-4
    (Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one shows strong inhibitory activity on leukotriene biosynthesis in human polymorphonuclear granulocytes, and it is very effective against mycobacteria.
    • ¥ 3940
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  • Glaucin B
    TN4135115458-73-6
    Glaucin B is a new bitter limonoid.
    • 询价
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  • 1-Methyl-2-undecyl-4(1H)-quinolone
    TN255359443-02-6
    1-Methyl-2-undecyl-4(1H)-quinolone, and dihydroevocarpine should also be served as the chemical markers together with evodiamine for the quality control of Evodia rutaecarpa (Juss.) Benth. 1-Methyl-2-undecyl-4(1H)-quinolone shows a selective inhibition of type B MAO (MAO-B) activity with the IC(50) value of 15.3 microM using a substrate kynuramine, but does not inhibit type A MAO (MAO-A) activity.It can mitigate high phosphate-induced human aortic valve interstitial cells (HAVICs) calcification by inhibiting phosphate cotransporter (PiT-1) gene expression. It also shows moderate antiangiogenic activity against human tumor cells.
    • ¥ 3230
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  • Flavaprin
    TN406153846-49-4
    Flavaprin是一种天然产物,属于芸香科三桠苦属,其产品编号为 TN4061,CAS号为 53846-49-4。Flavaprin可用作对照参考。
    • ¥ 14800
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  • 7-Isopentenyloxy-gamma-fagarine
    TN323723417-92-7
    7-Isopentenyloxy-gamma-fagarine has highly cytotoxicity against the MCF-7and Jurkat cell line. It has been used as a precursor for the chemical asymmetric synthesis of the enantiopure alkaloids: evoxine, anhydroevoxine and evodine.
    • ¥ 14980
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  • Limonexic acid
    TN444099026-99-0
    Limonexic acid shows antinociceptive actions , it produces dose-related inhibition of glutamate- and capsaicin-induced pain. Limonexic acid can effectively protect hepatocyte against CCl4-induced injury.
    • ¥ 17300
    5日内发货
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  • 12alpha-Hydroxyevodol
    TN2604120722-04-5
    12alpha-Hydroxyevodol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2604,CAS号为 120722-04-5。
    • ¥ 3940
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  • 1-Hydroxyrutaecarpine
    TN117353600-24-1
    1-Hydroxyrutaecarpine exhibits cytotoxicities (ED50 values < 4 microg mL) against P-388 or HT-29 cell lines in vitro.
    • ¥ 3710
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  • Hydroxyevodiamine
    TN17521238-43-3
    Hydroxyevodiamine is a natural product
    • ¥ 950
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  • Elasticamide
    TN2681154801-30-6
    (2S,3S,4R,2'R)-2-(2'-hydroxytetracosanoylamino)octadecane-1,3,4-triol shows selectively inhibitory activity against phospholipase A 2 (PLA 2) secreted from Crotalus adamenteus venom at concentration of 100 ug mL.
    • ¥ 33800
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  • 6-Acetonyl-N-methyl-dihydrodecarine
    TN31511253740-09-8
    6-Acetonyl- N -methyl-dihydrodecarine has mosquito larvicidal activity against the malaria vector Anopheles gambiae.
    • ¥ 3940
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  • Evodol
    TN163822318-10-1
    Evodol may as an anti-inflammatory agent or lead compound, it shows inhibitory activity on nitric oxide (NO) production in lipopolysaccharide -activated RAW264.7 macrophages. Evodol and limonin possess larvicidal activity against the Asian tiger mosquitoe
    • ¥ 4150
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  • 1-Methyl-2-nonylquinolin-4(1H)-one
    TN255268353-24-2
    1-Methyl-2-nonylquinolin-4(1H)-one has anti-inflammatory activity, it exhibits inhibitory activity on leukotriene biosynthesis in a bioassay using human polymorphonuclear granulocytes, with IC50 values of 12.1 microM.
    • ¥ 3090
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  • 1-Methyl-2-pentyl-4(1H)-quinolinone
    TN117522048-98-2
    1-Methyl-2-pentyl-4(1H)-quinolinone, a natural product,
    • ¥ 2289
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  • 5-Methoxy-2',3'-dehydromarmesin
    TN267354087-32-0
    5-Methoxy-2',3'-dehydromarmesin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2673,CAS号为 54087-32-0。
    • ¥ 5870
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  • Dihydroevocarpine
    TN109915266-35-0
    Dihydroevocarpine shows potent anti-Helicobacter pylori activity with the minimum inhibitory concentration (MIC) value of 10-20 microg ml. Dihydroevocarpine is a moderate modulator of p-glycoprotein (p-gp) activity; it shows more potent inhibitory effects against MAO-B compared to MAO-A.
    • ¥ 1390
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