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  • T9004TM2-115TM2 115,TM2115

    TM2-115 is a inhibitor of malaria parasite histone methyltransferases that results in rapid and irreversible parasite death [1].

    价 格：￥电议型 号：T9004产 地：中国大陆

  • T6S2115Ginkgolide Jinhibit,Ginkgolide J,Inhibitor

    Ginkgolide J has neuroprotective activity, it can prevent A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices.

    价 格：￥电议型 号：T6S2115产 地：中国大陆

  • T5360Eprotirome伊罗替罗；KB2115

    Eprotirome, a synthetic thyroid hormone mimetic, is a thyroid hormone receptor agonist.

    价 格：￥电议型 号：T5360产 地：中国大陆

  • T4657LWHI-P97 HCl 211555-05-4(free base)

    WHI-P97 HCl is a potent and selective JAK-3 inhibitor. WHI-P97 had an estimated Ki value of 0.09 microM from modeling studies and a measured IC50 value of 2.5 microM in EGFR kinase inhibition assays. WHI-P97 effectively inhibited the in vitro invasiveness

    价 格：￥电议型 号：T4657L产 地：中国大陆

  • T22115SM-7368SM 7368

    The NF-κB Activation Inhibitor III, controls the biological activity of NF-κB. It is primarily used for Inflammation/Immunology applications.

    价 格：￥电议型 号：T22115产 地：中国大陆

  • T21153Clothianidin噻虫胺；TI-435；TI435；Celero；TI 435

    Clothianidin, an insecticide, acts as an agonist of acetylcholine to stimulate nAChR, thereby activating post-synaptic acetylcholine receptors but not inhibiting AChE.

    价 格：￥电议型 号：T21153产 地：中国大陆

  • T21152Ac-Phe-NH2Ac Phe NH2；Ac Phe-NH2；Ac-Phe NH2

    Ac-Phe-NH2 is a non-competitive inhibitor of polyubiquitin chain elongation at Ki value of 8 ± 1.2 mM.

    价 格：￥电议型 号：T21152产 地：中国大陆

  • T2115PexidartinibPLX-3397

    Pexidartinib is a capsule formulation containing a small-molecule receptor tyrosine kinase (RTK) inhibitor of KIT, CSF1R and FLT3 with potential antineoplastic activity.

    价 格：￥电议型 号：T2115产 地：中国大陆

  • T19807Dithiazanine iodideAbminthic；Netocyd；Delvex；Telmide；NSC 221154；Vercidon

    Dithiazanine iodide is a benzothiazole. It has been used as an antinematodal agent. It also has been effective as a nanoparticle in treating glioblastoma.

    价 格：￥电议型 号：T19807产 地：中国大陆

  • T19802ZINC72115182

    N-(3-(5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonamide is a novel selective inhibitor. The DFG-in conformation of the B-Raf kinase V600E mutant is superior to the DFG-out conformation in colorectal cancer.

    价 格：￥电议型 号：T19802产 地：中国大陆

  • T12115MSC2360844

    MSC2360844 is a potent, orally active and selective inhibitor of PI3Kδ(IC50 of 145 nM).

    价 格：￥电议型 号：T12115产 地：中国大陆

  • T16380OGT 2115OGT 2115

    OGT 2115 is an effective and cell-permeable heparanase inhibitor (IC50: 0.4 μM). OGT 2115 also suppresses heparan sulfate degradation activity. OGT 2115 has anti-angiogenic properties (IC50: 1 μM).

    价 格：￥电议型 号：T16380产 地：美洲

  • T2115PexidartinibPexidartinib,PLX-3397,

    Pexidartinib is a capsule formulation containing a small-molecule receptor tyrosine kinase (RTK) inhibitor of KIT, CSF1R and FLT3 with potential antineoplastic activity.

    价 格：￥电议型 号：T2115产 地：美洲

  • T5360EprotiromeEprotirome,KB2115,

    Eprotirome, a synthetic thyroid hormone mimetic, is a thyroid hormone receptor agonist.

    价 格：￥电议型 号：T5360产 地：美洲

  • T82115ICMT-IN-29；化合物 ICMT-IN-29ICMT-IN-29

    ICMT-IN-29, also known as compound 66, effectively inhibits ICMT with an IC50 value of 0.019 μM [1].

    价 格：￥电议型 号：T82115产 地：中国大陆

  • T721155-Iminodaunorubicin hydrochloride化合物 5-Iminodaunorubicin hydrochloride盐酸5-亚氨基柔红霉素

    5-Iminodaunorubicin hydrochloride, a quinone-modified anthracycline, maintains antitumor efficacy. It induces concealed DNA strand breaks within cancer cells, mediated by protein interactions.

    价 格：￥电议型 号：T72115产 地：中国大陆

  • T6S2115Ginkgolide J；银杏内酯JBN 52024|||7-beta-Hydroxyginkgolide A；BN 52024|||7-beta-Hydroxyginkgolide A|||银杏内酯

    Ginkgolide J (BN 52024) has neuroprotective activity, it can prevent A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices.

    价 格：￥电议型 号：T6S2115产 地：中国大陆

  • T64279ODN 21158；化合物 ODN 21158ODN 21158

    ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.

    价 格：￥电议型 号：T64279产 地：中国大陆

  • T62115HBV-IN-24；化合物 HBV-IN-24HBV-IN-24

    HBV-IN-24 (compound (2 S, 6S)-1a) is a potent inhibitor of HBV. HBV-IN-24 is a strong inhibitor of HBV DNA (EC50: 0.6 nM), HBsAg (EC50: 0.6 nM) and HBeAg (EC50: 4.6 nM). antiviral effect and was able to improve neurotoxicity.

    价 格：￥电议型 号：T62115产 地：中国大陆

  • T5360Eprotirome；伊罗替罗KB2115；伊罗替罗|||KB2115

    Eprotirome (KB2115), a synthetic thyroid hormone mimetic, is a thyroid hormone receptor agonist.

    价 格：￥电议型 号：T5360产 地：中国大陆

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