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  • T8320J14cancer,inhibit,damage,Sulfiredoxin,J14,cytotoxicity,Reactive Oxygen Species,J 14,death,adenocarci

    J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 μM). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death

    价 格：￥电议型 号：T8320产 地：中国大陆

  • T27026LCJ-13,610 hydrochlorideCJ 13,610 hydrochloride,CJ13,610 hydrochloride

    CJ-13,610 hydrochloride is an orally active nonredox-type inhibitor of 5-LOX and can be used in studies about the prevention of untoward pathophysiological effects of LTs.

    价 格：￥电议型 号：T27026L产 地：中国大陆

  • T6847GSK-J1GSK-J1,inhibit,Inhibitor,Histone Demethylase,GSKJ1,GSK-J-1

    GSK-J1 is a highly potent H3K27 histone demethylase inhibitor with IC50 of 28 nM and 53 nM in cell-free assays for JMJD3 (KDM6B) and UTX (KDM6A), respectively, >10-fold selectivity over other tested demethylases.

    价 格：￥电议型 号：T6847产 地：中国大陆

  • T9936ZX-J-19JZXJ19J,ZX J 19J

    ZX-J-19J, an inhibitor of Cyclophilin J (CyPJ), demonstrates remarkable inhibition of tumor cell growth, comparable to cyclosporine A but much stronger than 5-fluorouracil.

    价 格：￥电议型 号：T9936产 地：中国大陆

  • T9104TJ191cancer,TJ 191,Apoptosis,PMBC,MOLT-3,CEM,inhibit,C8166,Inhibitor,MOLT-4,MT-2,TJ191,HSB-2,TJ-191,

    TJ191 is a selective anti-cancer agent, targeting low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.

    价 格：￥电议型 号：T9104产 地：中国大陆

  • TP1906L1DPC AJ1951 acetateDPC AJ1951 acetate

    DPC-AJ1951 acetate, a 14 amino acid peptide that acts as a potent agonist of the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR). And characterized the activity of DPC-AJ1951 acetate in ex vivo and in vivo assays of bone resorption[1].

    价 格：￥电议型 号：TP1906L1产 地：中国大陆

  • T9980AVJ16AVJ16

    AVJ16 as a member of the insulin growth factor 2 mRNA-binding protein family, binds to the mRNA of certain genes to regulate protein translation.

    价 格：￥电议型 号：T9980产 地：中国大陆

  • T5512JNJ16259685.TN.T 16259685

    JNJ16259685 is a selective mGluR1 antagonist, and inhibits the synaptic activation of mGluR1 in a concentration-dependent manner with IC50 of 19 nM.

    价 格：￥电议型 号：T5512产 地：中国大陆

  • T5464JNJ-10229570JNJ10229570；JNJ 10229570；UNII-N9IX402L35

    JNJ-10229570 is an antagonist of melanocortin receptor 1 (MC1R) and melanocortin receptor 5 (MC5R), which inhibits sebaceous gland differentiation and the production of sebum-specific lipids.

    价 格：￥电议型 号：T5464产 地：中国大陆

  • T4251GJ103 sodium salt

    GJ103 sodium salt is an active analog of the read-through compound GJ072.

    价 格：￥电议型 号：T4251产 地：中国大陆

  • T3448GJ103

    GJ103 sodium salt is an active analog of the read-through compound GJ072. Some GJ072 analogs (e.g., GJ103, GJ106, GJ109, and GJ111) consistently demonstrates their activities in all three PTCs by both FCATMpSer1981 and IRIF assays. GJ103 have similar read

    价 格：￥电议型 号：T3448产 地：中国大陆

  • T2684JNJ-1661010JNJ 1661010；Takeda-25；JNJ1661010

    JNJ-1661010 is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.

    价 格：￥电议型 号：T2684产 地：中国大陆

  • T19991N-desmethylmirtazapine米氮平杂质D；J1.061.658A；ORG3838；Normirtazapine；ORG 3838；N-Demethylmirtazapine；ORG-3

    N-desmethylmirtazapine is a metabolite of mirtazapine. N-desmethylmirtazapine is also commonly used as an anxiolytic, hypnotic, antiemetic, and appetite stimulant.

    价 格：￥电议型 号：T19991产 地：中国大陆

  • T1993J-147J147

    J147 is an experimental drug with reported effects against both Alzheimer´s disease and ageing in mouse models of accelerated aging. It is a curcumin derivative and a potent neurogenic and neuroprotective drug candidate initially developed for the treatme

    价 格：￥电议型 号：T1993产 地：中国大陆

  • T1993J147J147

    J147 is an experimental drug with reported effects against both Alzheimer´s disease and ageing in mouse models of accelerated aging. It is a curcumin derivative and a potent neurogenic and neuroprotective drug candidate initially developed for the treatme

    价 格：￥电议型 号：T1993产 地：美洲

  • T5464JNJ-10229570JNJ-10229570,JNJ10229570,UNII-N9IX402L35

    JNJ-10229570 is an antagonist of melanocortin receptor 1 (MC1R) and melanocortin receptor 5 (MC5R), which inhibits sebaceous gland differentiation and the production of sebum-specific lipids.

    价 格：￥电议型 号：T5464产 地：美洲

  • T8320J14；化合物J-14J-14；J-14

    J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 μM). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death

    价 格：￥电议型 号：T8320产 地：中国大陆

  • T82507Ecleralimab；化合物 EcleralimabCSJ-117|||NVP-CSJ117；CSJ-117|||NVP-CSJ117

    Ecleralimab (CSJ-117; NVP-CSJ117), a Fab-IgG1-λ2 monoclonal antibody, selectively targets thymic stromal lymphopoietin (TSLP). It is typically produced using a Chinese Hamster Ovary (CHO) cell expression system [1].

    价 格：￥电议型 号：T82507产 地：中国大陆

  • T80754YJ196；化合物 YJ196YJ196

    Compound YJ196 (Compound 59) serves as an inhibitor of New Delhi Metallo-β-lactamase-1 (NDM-1) [1].

    价 格：￥电议型 号：T80754产 地：中国大陆

  • T80433δ-Buthitoxin-Hj1a；化合物 δ-Buthitoxin-Hj1aδ-Buthitoxin-Hj1a

    δ-Buthitoxin-Hj1a, a scorpion-venom peptide, functions as a potent agonist for the NaV1.1 channel, exhibiting an EC50 value of 17 nM. It can be employed in research pertaining to Dravet syndrome (DS) [1].

    价 格：￥电议型 号：T80433产 地：中国大陆

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