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  • T3523Fostemsavir磷坦姆沙韦；BMS-663068

    BMS-663068 is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.

    价 格：￥电议型 号：T3523产 地：中国大陆

  • T34760SYR127063SYR-127063；BDBM92454；BDBM 92454；SYR 127063；BDBM-92454

    SYR127063 (BDBM92454) is a potent and selective HER2 inhibitor, binds to HER2 in a reactive conformation.

    价 格：￥电议型 号：T34760产 地：中国大陆

  • T3463NVP-ACC789ZK202650；ACC-789

    ACC-789 (NVP-ACC789; ZK-202650) is an effective, specific and orally active inhibitor of the VEGF receptor tyrosine kinases.

    价 格：￥电议型 号：T3463产 地：中国大陆

  • T3430PF-4136309PF 4136309；INCB8761；PF4136309

    INCB8761(PF-4136309) is a specific, effective, and orally bioavailable CCR2 antagonist.

    价 格：￥电议型 号：T3430产 地：中国大陆

  • T33639Neotame纽甜；NC-00723；NC00723；HSDB 7965；NC 00723

    Neotame is a white-colored, dipeptide methyl ester, which is found to be a highly potent and non-nutritive sweetener or flavour enhancer and hence finds applications in a variety of foods.

    价 格：￥电议型 号：T33639产 地：中国大陆

  • T3363Jervine蒜黎芦碱；Iervin；Jerwiny；11-Ketocyclopamine

    The biological activity of Jervine is mediated via its interaction with the 7 passes transmembrane protein Smoothened. Jervine binds with and inhibits smoothened, which is an integral part of the Hedgehog signaling pathways. With smoothened inhibited, the

    价 格：￥电议型 号：T3363产 地：中国大陆

  • T3360ZK 756326ZK756326 2HCl

    ZK 756326 is a selective, non-peptide CCR8 chemokine receptor agonist (IC50: 1.8 μM, in human; 2.6 μM, in mouse). Displays no activity at CCR4/5 and CXCR3/4 and shows higher 28-fold selectivity over 26 other GPCRs (less selective at α2A and 5-HT receptors

    价 格：￥电议型 号：T3360产 地：中国大陆

  • T32668Leucomalachite greenNSC36379；NSC-36379；NSC 36379；隐色孔雀绿

    Leucomalachite green is used in detecting latent bloodstains and in the forensic field because of convenience and cost/time-effectiveness.

    价 格：￥电议型 号：T32668产 地：中国大陆

  • T3263(6R,7S)-Cefminox sodium heptahydrate头孢米诺钠；Cefminox Sodium；Meicelin；Tencef；Alteporina

    Cefminox Sodium is a broad-spectrum, bactericidal cephalosporin antibiotic. It is especially effective against Gram-negative and anaerobic bacteria.

    价 格：￥电议型 号：T3263产 地：中国大陆

  • T3257UNC0638

    UNC0638 is an inhibitor of β-protein lysine methyltransferases G9a(IC50<15 nM) and GLP(IC50=19 nM) with excellent potency and selectivity over a wide range of epigenetic and non-epigenetic targets.

    价 格：￥电议型 号：T3257产 地：中国大陆

  • T31675EsaprazoleC/63

    Esaprazole has a dose - dependent cellular protective effect on the human gastric mucosa.

    价 格：￥电议型 号：T31675产 地：中国大陆

  • T3163PS 48

    PS 48 has been shown to be a PKB Kinase (PDK1) activator (Kd: 10.3 μM). This compound selectively binds to the PIF-binding pocket of PKB Kinase (PDK1).

    价 格：￥电议型 号：T3163产 地：中国大陆

  • T3119JNJ-63533054JNJ63533054；JNJ 63533054

    JNJ-63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM.

    价 格：￥电议型 号：T3119产 地：中国大陆

  • T3113ForetinibGSK089；EXEL-2880；GSK1363089；XL880

    Foretinib is a broad-spectrum tyrosine kinase inhibitor with IC50s of 0.4 nM and 0.9 nM for Met and KDR.

    价 格：￥电议型 号：T3113产 地：中国大陆

  • T3077SB 216763SB216763

    SB216763 is an effective and specific GSK-3α/β inhibitor (IC50: 34.3 nM).

    价 格：￥电议型 号：T3077产 地：中国大陆

  • T3076GLPG0634 analogGLPG0634 analogue

    GLPG0634 (analog) is a specific JAK1 inhibitor with IC50 of 10/28/810/116 nM for JAK1/2/3 and TYK2, respectively.

    价 格：￥电议型 号：T3076产 地：中国大陆

  • T3063PD173955PD 173955；PD-173955

    PD173955 is src family-selective tyrosine kinase inhibitor with IC50 of ~22 nM for Src, Yes and Abl kinase; less potent for FGFRα and no activity on InsR and PKC.

    价 格：￥电议型 号：T3063产 地：中国大陆

  • T3061LorlatinibPF-6463922；PF-06463922；劳拉替尼；Loratinib

    PF-06463922 is an orally available, ATP-competitive inhibitor of the receptor tyrosine kinases, anaplastic lymphoma kinase (ALK) and C-ros oncogene 1 (Ros1), with potential antineoplastic activity.

    价 格：￥电议型 号：T3061产 地：中国大陆

  • T2S16353-Isomangostin

    3-Isomangostin is an acetylcholinesterase selective inhibitor and a potent human aldose reductase inhibitor with an IC50 of 3.48 uM. 3-Isomangostin has free radical scavenging activity and inhibits MutT homolog 1 (MTH1) with an IC50 of 52 nM. It shows ant

    价 格：￥电议型 号：T2S1635产 地：中国大陆

  • T2S0663Humantenmine

    1. Humantenmine is a toxic compound isolated from Gelsemium elegans Benth . 2. Humantenmine and koumine may inhibit several CYP450 enzyme activities.

    价 格：￥电议型 号：T2S0663产 地：中国大陆

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