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  • T670711,2-Dipalmitoyl-sn-glycero-3-phospho-rac-glycerol sodium salt；化合物 1,2-Dipalmitoyl-sn-glycero-3-phosp

    1,2-Dipalmitoyl-sn-glycero-3-phospho-rac-glycerol sodium salt is a useful organic compound for research related to life sciences and the catalog number is T67071.

    价 格：￥电议型 号：T67071产 地：中国大陆

  • T6704TG 100713；化合物TG100713TG100713；TG100713

    TG 100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.

    价 格：￥电议型 号：T6704产 地：中国大陆

  • T66071N-[5-Bromomethyl-4-(4-fluorophenyl)-6-isopropylpyrimidine-2-yl]-N-methylmethane sulfonamide；化合物 N-[5

    N-[5-Bromomethyl-4-(4-fluorophenyl)-6-isopropylpyrimidine-2-yl]-N-methylmethane sulfonamide is a useful organic compound for research related to life sciences. The catalog number is T66071 and the CAS number is 799842-07-2.

    价 格：￥电议型 号：T66071产 地：中国大陆

  • T650711-(4-Bromophenyl)piperazine (hydrochloride)；化合物 1-(4-Bromophenyl)piperazine (hydrochloride)1-(4-Brom

    1-(4-Bromophenyl)piperazine (hydrochloride) is a useful organic compound for research related to life sciences. The catalog number is T65071 and the CAS number is 68104-62-1.

    价 格：￥电议型 号：T65071产 地：中国大陆

  • T64206VGD071；化合物 VGD071VGD071

    VGD071, a compound that targets sortilin, presents a promising avenue for forthcoming research utilizing mouse models of breast cancer.

    价 格：￥电议型 号：T64206产 地：中国大陆

  • T64071Antitumor agent-42；化合物 Antitumor agent-42Antitumor agent-42

    Antitumor agent-42 inhibits microtubule multimerisation and NO release, exhibiting anti-angiogenic, colony-forming and apoptosis-inducing effects.

    价 格：￥电议型 号：T64071产 地：中国大陆

  • T63071CDK6/PIM1-IN-1；化合物 CDK6/PIM1-IN-1CDK6/PIM1-IN-1

    CDK6/PIM1-IN-1 is a balanced, potent, dual CDK6 (IC50: 39 nM) and PIM1 (IC50: 88 nM) inhibitor. CDK6/PIM1-IN-1 showed inhibitory effect on CDK4 with IC50 value of 3.6 nM. CDK6/PIM1-IN-1 can significantly inhibit the proliferation of acute myeloid leukemia (AML) cells, arrest the cell cycle in G1 phase and induce cell apoptosis. CDK6/PIM1-IN-1 showed anti-AML activity.

    价 格：￥电议型 号：T63071产 地：中国大陆

  • T6278Sotrastaurin；索曲妥林AEB071；索曲妥林|||AEB071

    Sotrastaurin (AEB071) is a potent pan-PKC inhibitor (Kis: 0.95/0.64/2.1/3.2/1.8/0.22 nM for PKCα/βI/δ/ε/η/θ).

    价 格：￥电议型 号：T6278产 地：中国大陆

  • T62071VEGFR-2-IN-16；化合物 VEGFR-2-IN-16VEGFR-2-IN-16

    VEGFR-2-IN-16 (Compound 15b) is a potent inhibitor of VEGFR-2 (IC50: 86.36 nM) that exhibits antitumour effects.

    价 格：￥电议型 号：T62071产 地：中国大陆

  • T6108Ki16425；化合物Ki16425Debio 0719；Debio 0719

    Ki16425 (Debio 0719) is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM, respectively.

    价 格：￥电议型 号：T6108产 地：中国大陆

  • T61071AX-024；化合物 AX-024AX-024

    AX-024 is a novel chemical compound that acts as an orally available inhibitor of the TCR-Nck interaction. Its primary mechanism of action is the selective inhibition of T cell activation triggered by TCR stimulation. With an IC50 value of approximately 1 nM, AX-024 effectively modulates cell signaling by specifically targeting SH3 domains. Additionally, AX-024 demonstrates desirable characteristics such as low acute toxicity, high potency, and excellent selectivity. Notably, it exhibits strong

    价 格：￥电议型 号：T61071产 地：中国大陆

  • T60719AR antagonist 3；化合物 AR antagonist 3AR antagonist 3

    When administered intratumorally, AR antagonist 3 shows effective inhibition on the growth of tumor. AR antagonist 3 is a potent and selective antagonist of androgen receptor (AR) with an IC 50 of 0.47 μM. AR antagonist 3 dose-dependently decrease the FRET signal with an IC50 of 18.05 μM [1].

    价 格：￥电议型 号：T60719产 地：中国大陆

  • T607183-IN-PP1；化合物 3-IN-PP13-IN-PP1

    3-IN-PP1, a potent protein kinase D (PKD) inhibitor, exhibits pan-PKD inhibitory activity with IC50 values of 108 nM for PKD1, 94 nM for PKD2, and 108 nM for PKD3. Additionally, it serves as a broad-spectrum anticancer agent by inhibiting the growth of various tumor cells. 3-IN-PP1 is utilized in cancer research [1].

    价 格：￥电议型 号：T60718产 地：中国大陆

  • T60717Phenolphthalol；化合物 PhenolphthalolPhenolphthalol

    Phenolphthalol is estrogenically active which is also a laxative in drug preparations [1].

    价 格：￥电议型 号：T60717产 地：中国大陆

  • T60716Antitubercular agent-28；化合物 Antitubercular agent-28Antitubercular agent-28

    Antitubercular agent-28 (compound 2) has antimycobacterial activity for resistant isolates of Mycobacterium tuberculosis H37Rv. Antitubercular agent-28 is a potent antitubercular agent with an MIC value of 4.5 μM, an IC 50 value of 1.5 μM, and an IC 90 value of 2.5 μM. Antitubercular agent-28 shows effective intracellular antimycobacterial activity with low cytotoxicity [1].

    价 格：￥电议型 号：T60716产 地：中国大陆

  • T60715α-Glucosidase-IN-4；α-Glucosidase抑制剂4α-Glucosidase-IN-4

    α-Glucosidase-IN-4 is a potent α-glucosidase inhibitor with antihypertensive and hypoglycemic activity.

    价 格：￥电议型 号：T60715产 地：中国大陆

  • T60714gp120-IN-2；化合物 gp120-IN-2gp120-IN-2

    gp120-IN-2 (compound 4i) exhibits anti-HIV-1 activity which is a potent inhibitor of HIV-1 gp120 with an IC 50 of 7.5 μM and CC 50 of 112.93 μM. gp120-IN-2 dose-dependently shows cytotoxicity in SUP-T1 cells [1].

    价 格：￥电议型 号：T60714产 地：中国大陆

  • T60713TK-129；化合物 TK-129TK-129

    TK-129 is an orally active, potent inhibitor of KDM5B with IC 50 of 44 nM that is low-toxicity. TK-129 shows cardioprotective effects by inhibiting KDM5B and blocking the KDM5B -associated Wnt pathway. TK-129 can be used in cardiovascular disease studies which reduce isoprenaline-induced myocardial remodelling and fibrosis in vivo as well as reduce ang II-induced activation of cardiac fibroblasts in vitro [1].

    价 格：￥电议型 号：T60713产 地：中国大陆

  • T60712MAO-B-IN-17；MAO-B抑制剂17MAO-B-IN-17

    MAO-B-IN-17 is a selective and potent monoamine oxidase B (MAO-B) inhibitor (IC50: 5.08 μM) for the study of central nervous system disorders like Parkinson´s.

    价 格：￥电议型 号：T60712产 地：中国大陆

  • T60711Avibactam sodium hydrate；化合物 Avibactam sodium hydrateAvibactam sodium hydrate

    Avibactam sodium hydrate (NXL-104 hydrate) is a covalent and reversible inhibitor of β-lactamase that does not contain a β-lactam core. Avibactam sodium hydrate inhibits β-lactamase CTX-M-15 and TEM-1 with IC 50 s of 5 nM and 8 nM, respectively.

    价 格：￥电议型 号：T60711产 地：中国大陆

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