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  • T24417Yakuchinone A益智酮甲；Yakuchinone-A

    Yakuchinone A is a natural product isolated from Alpinia oxyphylla Miquel. Yakuchinone-A has strong inhibitory effects on the synthesis of prostaglandins and leukotrienes in vitro. Yakuchinone A inhibits the expression of cyclooxygenase-2 and of inducible

    价 格：￥电议型 号：T24417产 地：中国大陆

  • T19895ChlorotoluronDicuran；Dikurin；绿麦隆

    Chlorotoluron is a pheylurea herbicide. Chlorotoluron has been used to control the growth of broad-leaved weeds in winter wheat, rye, barley, and triticale crops.

    价 格：￥电议型 号：T19895产 地：中国大陆

  • T11076Dooku1

    Dooku1 is an analog of Yoda1 and a selective antagonist of endogenous Piezo1 channels. Dooku1 inhibits Ca2+ entry induced by 2μMYoda1 with IC50 values of 1.3μM (in HEK 293 cells) and 1.5μM (in HUVEC). Dooku1 inhibits Yoda1-induced aortic relaxation.

    价 格：￥电议型 号：T11076产 地：中国大陆

  • T0720Gallamine triethiodide加拉碘铵；三碘季胺酚；Flaxedil；Benzkurin

    Gallamine Triethiodide, a synthetic inhibiting drug, is nondepolarizing.

    价 格：￥电议型 号：T0720产 地：中国大陆

  • T0720Gallamine triethiodideGallamine triethiodide,Flaxedil,Benzkurin

    Gallamine Triethiodide, a synthetic inhibiting drug, is nondepolarizing.

    价 格：￥电议型 号：T0720产 地：美洲

  • T11076Dooku1Dooku1

    Dooku1 is an analog of Yoda1 and a selective antagonist of endogenous Piezo1 channels. Dooku1 inhibits Ca2+ entry induced by 2μMYoda1 with IC50 values of 1.3μM (in HEK 293 cells) and 1.5μM (in HUVEC). Dooku1 inhibits Yoda1-induced aortic relaxation.

    价 格：￥电议型 号：T11076产 地：美洲

  • T15498HOKU-81HOKU-81,4-Hydroxytulobuterol,

    HOKU-81is a new bronchodilator and is one of the metabolites of tulobuterol.

    价 格：￥电议型 号：T15498产 地：美洲

  • T15673KU 59403KU 59403

    KU 59403 is an effective ATM inhibitor (IC50: 3 nM, 9.1 μM, and 10 μM for ATM, DNA-PK, and PI3K, respectively).

    价 格：￥电议型 号：T15673产 地：美洲

  • T2474KU-60019KU-60019,KU60019,KU 60019

    Ku-60019 is a potent, reversible inhibitor of ATM kinase (IC50: 6.3 nM). It is much less effective or without effect against a panel of 229 other kinases.

    价 格：￥电议型 号：T2474产 地：美洲

  • T2475KU0063794KU0063794

    KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTORC2.

    价 格：￥电议型 号：T2475产 地：美洲

  • T2685KU55933KU55933,ATM Kinase Inhibitor,

    KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.

    价 格：￥电议型 号：T2685产 地：美洲

  • T2726SinomenineSinomenine,Cucoline,Kukoline

    Sinomenine is a pure alkaloid isolated from the Sinomenium acutum, is utilized in the treatment of rheumatism and arthritis.

    价 格：￥电议型 号：T2726产 地：美洲

  • T4S0290Chikusetsusaponin IVChikusetsusaponin IV,Araloside A,

    1. Chikusetsusaponin IV might relieve cutaneous symptoms caused by excessive apoptotic cell death in the skin through the Fas/FasL pathway.

    价 格：￥电议型 号：T4S0290产 地：美洲

  • T6276NU7441NU7441,KU-57788,

    NU7441 (KU-57788) is a highly effective and specific DNA-PK inhibitor (IC50: 14 nM).

    价 格：￥电议型 号：T6276产 地：美洲

  • T83948Sakura 6；化合物 Sakura 6Sakura 6

    Sakura 6, a synthetic serotonin transporter (SERT)-binding peptide, enhances the interaction between SERT and neuronal nitric oxide synthase. This interaction decreases SERT activity and its presence on the cell surface, augments auto-inhibition, lowers synaptic 5-HT release, and diminishes activity in the dorsal raphe nucleus, ultimately inducing an acute depressive phenotype in a mouse depression model.

    价 格：￥电议型 号：T83948产 地：中国大陆

  • T8376PKCβ inhibitor 1；化合物PKCβ inhibitor 1KUN79359；KUN79359

    PKCβ inhibitor 1 (KUN79359)(KUN79359) is a potent, selective and ATP-competitive inhibitor of PKC isozymes(IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2, respectively).

    价 格：￥电议型 号：T8376产 地：中国大陆

  • T82739Chikusaikoside Ⅱ；化合物 Chikusaikoside ⅡChikusaikoside Ⅱ

    Chikusaikoside II, a natural product, is isolated from Bupleurum longeradiatum [1].

    价 格：￥电议型 号：T82739产 地：中国大陆

  • T8214Kushenol E；苦参醇EFlemiphilippinin D；苦参醇E|||Flemiphilippinin D

    Kushenol E (Flemiphilippinin D) is a class of flavonoids isolated from Sophora flavescens. It is a non-competitive IDO1 inhibitor (IC50: 7.7 μM, Ki: 9.5 μM), has anti-tumor activity.

    价 格：￥电议型 号：T8214产 地：中国大陆

  • T81972Kuwanon K；化合物 Kuwanon KKuwanon K

    Kuwanon K, a natural product, is extractable from Morus Lhou [1].

    价 格：￥电议型 号：T81972产 地：中国大陆

  • T81971Kuwanon O；化合物 Kuwanon OKuwanon O

    Kuwanon O, a flavonoid derivative featuring a fused dihydrochalcone segment, is extractable from the root bark of Morus lhou (set.) Koidz [1].

    价 格：￥电议型 号：T81971产 地：中国大陆

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