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  • T4254TM5441

    TM5441 is an orally bioavailable inhibitor of plasminogen activator inhibitor 1 (PAI-1).

    价 格：￥电议型 号：T4254产 地：中国大陆

  • T4253Skp2 Inhibitor C1SKPin C1

    Skp2 Inhibitor C1(SKPin C1) is a specific small molecule inhibitor of Skp2-mediated p27 degradation.

    价 格：￥电议型 号：T4253产 地：中国大陆

  • T4252ML327

    ML327 is a blocker of MYC which can also de-repress E-cadherin transcription and reverse Epithelial-to-Mesenchymal Transition (EMT).

    价 格：￥电议型 号：T4252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

  • T4250Bilastine比拉斯汀；Bilaxten

    Bilastine is a novel new-generation antihistamine that is highly selective for the H1 histamine receptor, has a rapid onset and prolonged duration of action.

    价 格：￥电议型 号：T4250产 地：中国大陆

  • T39202CZC-54252 hydrochloride

    CZC-54252 hydrochloride is a potent and selective LRRK2 inhibitor with IC 50 s of 1.28 nM and 1.85 nM for wild-type and G2019S LRRK2 , respectively. G2019S LRRK2 -induced human neuronal injury is attenuated by CZC-54252 hydrochloride with an EC 50 of ~1 n

    价 格：￥电议型 号：T39202产 地：中国大陆

  • T2425KPT185KPT 185；KPT-185

    KPT-185 is a selective CRM1 inhibitor, inducing apoptosis, cell-cycle arrest.

    价 格：￥电议型 号：T2425产 地：中国大陆

  • T22689CP94253 hydrochlorideCP 94253 hydrochloride

    CP94253 hydrochloride is a potent, selective and centrally active agonist of 5-HT1B receptor with Ki of 2 nM. The Kis are 89, 49, 860, and 1600 nM for 5-HT1A, 5-HT1D, 5-HT1C and 5-HT2 receptors, respectively.

    价 格：￥电议型 号：T22689产 地：中国大陆

  • T22425SevofluraneFluoromethyl；七氟烷

    Sevoflurane, a noncompetitive inhibitor of 5-HT3 receptor, acts as a low-soluble inhalation anesthetics.

    价 格：￥电议型 号：T22425产 地：中国大陆

  • T21425MephenytoinPhenantoin；Methylphenetoin；Methoin；Mesantoin；Insulton；美芬妥因

    Mephenytoin is an anticonvulsant and a substrate of CYP2C19 and CYP2B6.

    价 格：￥电议型 号：T21425产 地：中国大陆

  • T2022CZC-54252CZC 54252；CZC54252

    CZC-54252 is a potent inhibitor of LRRK2.

    价 格：￥电议型 号：T2022产 地：中国大陆

  • T196618-Chloroadenosine8-Cl-Ado；NSC354258；8Chloroadenosine；NSC-354258；NSC 354258；8 Chloroadenosine；8-氯腺嘌呤核

    8-Chloroadenosine is a 5´ AMP-activated protein kinase agonist potentially for the treatment of chronic lymphocytic leukemia. 8-chloroadenosine activity is associated with inhibition of the mTOR pathway.8-Chloroadenosine is a nucleoside analog; metabolize

    价 格：￥电议型 号：T19661产 地：中国大陆

  • T16859SBI-425

    SBI-425 is a potent and selective tissue-nonspecific alkaline phosphatase inhibitor. Long-term administration of SBI-425 effectively reaches and inhibits TNAP in the vasculature, improving cardiovascular parameters and survival at a dose that does not cau

    价 格：￥电议型 号：T16859产 地：中国大陆

  • T15595LIRL-1620 acetateIRL-1620 acetate（142569-99-1 free base）

    IRL-1620 acetate is an effective and selective agonist of Endothelin B receptor (ETB) with a Ki of 16 pM which is more selective than ETA with a Ki of 19 μM.

    价 格：￥电议型 号：T15595L产 地：中国大陆

  • T15216EML 425

    EML 425 is a potent and selective inhibitor of CREB binding protein (CBP)/p300 (IC50s: 2.9 and 1.1 μM, respectively).

    价 格：￥电议型 号：T15216产 地：中国大陆

  • T1425Pemirolast potassium吡嘧司特钾；TWT-8152；BMY 26517

    Pemirolast Potassium is the potassium salt form of pemirolast, a pyrimidinone derivative with antiallergic property. Pemirolast potassium exerts its action by blocking the antigen-mediated calcium ion influx into mast cells.

    价 格：￥电议型 号：T1425产 地：中国大陆

  • T12425PF-06424439 methanesulfonate

    PF-06424439 methanesulfonate is an oral, potent and selective imidazopyridine diacylglycerol acyltransferase 2 (DGAT2) inhibitor(IC50 of 14 nM)[1]. PF-06424439 methanesulfonate is slowly reversible, time-dependent inhibitor, which inhibits DGAT2 in a nonc

    价 格：￥电议型 号：T12425产 地：中国大陆

  • T10550Bisindolylmaleimide X hydrochlorideRo31-8425 hydrochloride；BIM-X hydrochloride

    Bisindolylmaleimide X hydrochloride (BIM-X hydrochloride) is a potent and selective PKC inhibitor. It is also a potent CDK2 antagonist (IC50: 200 nM).

    价 格：￥电议型 号：T10550产 地：中国大陆

  • T10425AZ084

    AZ084 is a potent, selective, allosteric, and oral active CCR8 antagonist (Ki: 0.9 nM). It has the potential to treat asthma.

    价 格：￥电议型 号：T10425产 地：中国大陆

  • T0727Piperonyl butoxideButacide；Ethanol butoxide；ENT-14250；Pyrenone 606；增效醚

    Piperonyl butoxide is an insecticide synergist, particularly for rotenone and pyrethroids.

    价 格：￥电议型 号：T0727产 地：中国大陆

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