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  • T22456Voreloxin hydrochloride(3S-反式)-1,4-二氢-7-[3-甲氧基-4-(甲基氨基)-1-吡咯烷基]-4-氧代-1-(2-噻唑基)-1,8-萘啶-3-羧酸单盐酸盐；SNS-5

    Voreloxin hydrochloride is a potent inhibitor of Topoisomerase II with broad-spectrum anti-tumor activity.

    价 格：￥电议型 号：T22456产 地：中国大陆

  • T22106MLS-573151

    MLS-573151 is a selective inhibitor of GTPase Cdc42(EC50 of 2 μM). It is inactive against other GTPases family members, such as Rab2, Rab7, H-Ras, Rac1, Rac 2 and RhoA wild-type. MLS-573151 acts by blocking the binding of GTP to Cdc42.

    价 格：￥电议型 号：T22106产 地：中国大陆

  • T2204DiaveridineCCRIS-3784；EGIS-5645；AI3-23935；二氨藜芦啶；敌菌净

    Diaveridine (DVD) is a popular antibacterial synergist that is widely used in combination with sulfonamide. It has been reported to be genotoxic to mammalian cells, but more studies are required to clarify this.

    价 格：￥电议型 号：T2204产 地：中国大陆

  • T20689TemocaprilatRNH5139；RS-5139；RNH 5139；RS5139；RS 5139；RNH-5139

    Temocaprilat is an Angiotensin-converting Enzyme (ACE) inhibitor. Temocaprilat is effectively excreted in bile via cMOAT that is deficient in EHBR and that many of other ACE inhibitors have low affinity for cMOAT.

    价 格：￥电议型 号：T20689产 地：中国大陆

  • T1736ApixabanBMS-562247-01；阿哌沙班

    Apixaban is an orally active inhibitor of coagulation factor Xa with anticoagulant activity. Apixaban directly inhibits factor Xa, thereby interfering with the conversion of prothrombin to thrombin and preventing the formation of cross-linked fibrin clots

    价 格：￥电议型 号：T1736产 地：中国大陆

  • T16348NS5806NS-5806

    NS5806 is an effective potassium current activator. NS5806 slows KV4.3 and KV4.2 current decay in channel complexes containing KChIP2. NS5806 enhances KV4.3/KChIP2 peak current amplitudes (EC50: 5.3 μM).

    价 格：￥电议型 号：T16348产 地：中国大陆

  • T12584PXS-5120A

    PXS-5120A is an irreversible fluoroallylamine Lysyl Oxidase-like 2/3 (LOXL2/3) inhibitor with anti-fibrotic activity.

    价 格：￥电议型 号：T12584产 地：中国大陆

  • T11285FIDAS-5

    FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-5 has anticancer activities. FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.

    价 格：￥电议型 号：T11285产 地：中国大陆

  • T0672Pravastatin sodium普伐他汀钠；CS-514 Sodium；CS-514 (sodium)

    Pravastatin sodium, an HMG-CoA reductase inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM.

    价 格：￥电议型 号：T0672产 地：中国大陆

  • T0147Clemastine fumarateMeclastine fumarate；Meclastine (fumarate)；HS-592 (fumarate)；富马酸氯马斯汀

    Clemastine Fumarate is a synthetic ethanolamine with anticholinergic, sedative, and histamine H1 antagonistic properties.

    价 格：￥电议型 号：T0147产 地：中国大陆

  • T0147Clemastine fumarateClemastine fumarate,Meclastine (fumarate),HS-592 (fumarate)

    Clemastine Fumarate is a synthetic ethanolamine with anticholinergic, sedative, and histamine H1 antagonistic properties.

    价 格：￥电议型 号：T0147产 地：美洲

  • T0672Pravastatin sodiumPravastatin sodium,CS-514 (sodium),CS-514 Sodium

    Pravastatin sodium, an?HMG-CoA reductase?inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM.

    价 格：￥电议型 号：T0672产 地：美洲

  • T11285FIDAS-5FIDAS-5

    ?FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding.?FIDAS-5 has anticancer activities.?FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.

    价 格：￥电议型 号：T11285产 地：美洲

  • T11832Ledipasvir D-tartrateLedipasvir D-tartrate,GS-5885 D-tartrate,

    Ledipasvir D-tartrate with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon.?is an inhibitor of the hepatitis C virus NS5A.

    价 格：￥电议型 号：T11832产 地：美洲

  • T14124ADAMTS-5 InhibitorADAMTS-5 Inhibitor

    ADAMTS-5 Inhibitor is a potent ADAMTS-5 (aggrecanase-2) inhibitor, with an IC50 of 1.1 ?M. ADAMTS-5 Inhibitor shows >40-fold functional selectivity over ADAMTS-4 (aggrecanase-1)[1].

    价 格：￥电议型 号：T14124产 地：美洲

  • T14674BMS-509744BMS-509744

    BMS-509744 is an inhibitor of ATP competitive Itk (IC50: 19 nM).

    价 格：￥电议型 号：T14674产 地：美洲

  • T14675BMS-564929BMS-564929

    BMS-564929 is an androgen receptor (AR) agonist. Which binds to androgen receptor (AR) with a Ki of 2.11±0.16 nM.

    价 格：￥电议型 号：T14675产 地：美洲

  • T1736ApixabanApixaban,BMS-562247-01,

    Apixaban is an orally active inhibitor of coagulation factor Xa with anticoagulant activity. Apixaban directly inhibits factor Xa, thereby interfering with the conversion of prothrombin to thrombin and preventing the formation of cross-linked fibrin clots

    价 格：￥电议型 号：T1736产 地：美洲

  • T2204DiaveridineDiaveridine,EGIS-5645,AI3-23935

    Diaveridine (DVD) is a popular antibacterial synergist that is widely used in combination with sulfonamide. It has been reported to be genotoxic to mammalian cells, but more studies are required to clarify this.

    价 格：￥电议型 号：T2204产 地：美洲

  • T2389DapagliflozinDapagliflozin,BMS-512148,

    Dapagliflozin is a selective sodium-glucose co-transporter subtype 2 (SGLT2) inhibitor with antihyperglycemic activity.

    价 格：￥电议型 号：T2389产 地：美洲

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