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  • T11438GNE-1858

    GNE-1858 is an ATP-competitive hematopoietic progenitor kinase-1 (HPK1) inhibitor (IC50s of 1.9 nM, 1.9 nM, and 4.5 nM for wild-type and the active mimetic mutants HPK1-TSEE and HPK1-SA).

    价 格：￥电议型 号：T11438产 地：中国大陆

  • T101856-Phosphogluconic acid

    6-Phosphogluconic acid is a potent and competitive inhibitor of phosphoglucose isomerase (PGI).The activity of phosphoglucose isomerase was inhibited intensely and competitively by 6-Phosphogluconic acid, with an apparent Ki of 0.048 mM for glucose 6-phos

    价 格：￥电议型 号：T10185产 地：中国大陆

  • T0455Clozapine氯氮平；LX 100-129；HF 1854

    Clozapine is a tricylic dibenzodiazepine, classified as an atypical antipsychotic agent. It binds several types of central nervous system receptors, and displays a unique pharmacological profile. Clozapine is a serotonin antagonist, with strong binding to

    价 格：￥电议型 号：T0455产 地：中国大陆

  • T0209Loperamide hydrochloride盐酸洛哌丁胺；ADL 2-1294；Loperamide HCl；R-18553 (hydrochloride)

    Loperamide Hydrochloride is a synthetic, piperidine derivative and opioid agonist with antidiarrheal activity.

    价 格：￥电议型 号：T0209产 地：中国大陆

  • T0195Secnidazole塞克硝唑；PM-185184；RP-14539

    Secnidazole is a second-generation 5-nitroimidazole antimicrobial that is structurally related to other 5-nitroimidazoles including [DB00916] and [DB00911], but displays improved oral absorption and longer terminal elimination half-life than antimicrobial

    价 格：￥电议型 号：T0195产 地：中国大陆

  • T0185EscitalopramSeroplex；S-(+)-Citalopram；(S)-Citalopram；依他普仑；艾司西酞普兰

    Escitalopram is a furancarbonitrile that is one of the SEROTONIN UPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from tardive dyskinesia in

    价 格：￥电议型 号：T0185产 地：中国大陆

  • T0107Halcinonide哈西奈德；氯氟舒松；Halcimat；Halcinonida；Halciderm；SQ-18566

    Halcinonide, a high-efficiency corticosteroid, is served as an anti-inflammatory agent used in topical preparations.

    价 格：￥电议型 号：T0107产 地：中国大陆

  • T0107HalcinonideHalcinonide,SQ-18566,Halciderm

    Halcinonide, a high-efficiency corticosteroid, is served as an anti-inflammatory agent used in topical preparations.

    价 格：￥电议型 号：T0107产 地：美洲

  • T0195SecnidazoleSecnidazole,PM-185184,RP-14539

    Secnidazole is a second-generation 5-nitroimidazole antimicrobial that is structurally related to other 5-nitroimidazoles including [DB00916] and [DB00911], but displays improved oral absorption and longer terminal elimination half-life than antimicrobial

    价 格：￥电议型 号：T0195产 地：美洲

  • T0209Loperamide hydrochlorideLoperamide hydrochloride,R-18553 (hydrochloride),Loperamide HCl

    Loperamide Hydrochloride is a synthetic, piperidine derivative and opioid agonist with antidiarrheal activity.

    价 格：￥电议型 号：T0209产 地：美洲

  • T0455ClozapineClozapine,HF 1854,LX 100-129

    Clozapine is a tricylic dibenzodiazepine, classified as an atypical antipsychotic agent. It binds several types of central nervous system receptors, and displays a unique pharmacological profile. Clozapine is a serotonin antagonist, with strong binding to

    价 格：￥电议型 号：T0455产 地：美洲

  • T11607ICI 118,551 hydrochlorideICI 118,551 hydrochloride,ICI 118551 hydrochloride,

    ICI 118,551 ?is a highly selective β2 adrenergic receptor antagonist, with Kis of 0.7, 49.5 and 611 nM for β2, β1 and β3 receptors, respectively.?

    价 格：￥电议型 号：T11607产 地：美洲

  • T1185RofecoxibRofecoxib,MK 966,MK-0966

    Rofecoxib binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in an inhibition of the conversion of arachidonic acid to prostaglandins. Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with anti-inflammatory, antipyret

    价 格：￥电议型 号：T1185产 地：美洲

  • T11852LiclotideLiclotide,Linaclotide,

    Linaclotide?developed for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) and chronic constipation, and is a potent and selective guanylate cyclase C agonist.

    价 格：￥电议型 号：T11852产 地：美洲

  • T11854LipofermataLipofermata

    Lipofermata is a fatty acid transporter protein (FATP) inhibitor that prevents lipid transport to melanoma cells and reduces melanoma growth and invasion.

    价 格：￥电议型 号：T11854产 地：美洲

  • T11857LIT-001LIT-001

    LIT-001 improves social interaction in a mouse model of autism.LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist (EC50=55 nM;?Ki=226 nM).

    价 格：￥电议型 号：T11857产 地：美洲

  • T11858Lith-O-AspLith-O-Asp

    Lith-O-Asp is a sialytransferase (ST) inhibitor,(IC50s：12-37 μM).

    价 格：￥电议型 号：T11858产 地：美洲

  • T11859Litronesib RacemateLitronesib Racemate,LY-2523355 Racemate,KF-89617 Racemate

    Litronesib is a selective, allosteric inhibitor of kinesin Eg5.Litronesib (Racemate) is the racemate of litronesib.

    价 格：￥电议型 号：T11859产 地：美洲

  • T11859LLitronesibLitronesib,LY-2523355,KF-89617

    Litronesib is a selective inhibitor of mitosis-specific kinesin Eg5. It also has antitumor activity.

    价 格：￥电议型 号：T11859L产 地：美洲

  • T15185LucitanibLucitanib,E-3810,

    Lucitanib (E-3810) is a novel dual VEGFR and FGFR inhibitor. It potently and selectively inhibits VEGFR1, VEGFR2, VEGFR3, FGFR1 and FGFR2 (IC50s: 7 nM, 25 nM, 10 nM, 17.5 nM, and 82.5 nM, respectively).

    价 格：￥电议型 号：T15185产 地：美洲

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