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  • T367892-Methylcyclohexanone

    2-Methylcyclohexanone is an endogenous metabolite.

    价 格：￥电议型 号：T36789产 地：中国大陆

  • T367882-Methylacetophenone

    2-Methylacetophenone is an endogenous metabolite.

    价 格：￥电议型 号：T36788产 地：中国大陆

  • T367872-hydroxymethyl benzoic acid

    2-hydroxymethyl benzoic acid is a principal metabolite of the phthalidyl moiety in man.

    价 格：￥电议型 号：T36787产 地：中国大陆

  • T367862-Hydroxy-4-methylbenzaldehyde

    2-Hydroxy-4-methylbenzaldehyde is an endogenous metabolite.

    价 格：￥电议型 号：T36786产 地：中国大陆

  • T3678EntrectinibRXDX-101；NMS-E628；恩曲替尼

    Entrectinib is an inhibitor of TrkA (IC50: 1.7 nM), TrkB (IC50: 0.1 nM), and TrkC (IC50: 0.1 nM), as well as anaplastic lymphoma kinase (ALK; IC50: 1.6 nM) and C-ros oncogene 1 (ROS1; IC50: 0.2 nM). Entrectinib blocks proliferation of ALK-dependent cell l

    价 格：￥电议型 号：T3678产 地：中国大陆

  • T36670JNJ-67856633

    JNJ-67856633 is an orally active, first-in-class, potent, selective and allosteric MALT1 protease inhibitor. JNJ-67856633 in some cases lead to tumor stasis[1][2][3].

    价 格：￥电议型 号：T36670产 地：中国大陆

  • T3633CrenigacestatLY3039478

    LY3039478 is an orally bioavailable Notch inhibitor with an IC50 of ~1 nM in most of the tumor cell lines tested. LY3039478 effectively inhibits mutant Notch receptor activity. In a xenograft tumor model, LY3039478 inhibited expression of Notch-regulated

    价 格：￥电议型 号：T3633产 地：中国大陆

  • T3620SolcitinibGSK-2586184；GLPG-0778；索西替尼

    Solcitinib (GSK2586184, GLPG0778) is a JAK1 inhibitor. Solcitinib may be potentially used for the treatment of psoriasis, ulcerative colitis, and systemic lupus erythematosus.

    价 格：￥电议型 号：T3620产 地：中国大陆

  • T3618GSK-2881078GSK2881078；GSK 2881078

    GSK2881078 is a selective androgen receptor modulator (SARM) that is being evaluated for effects on muscle growth and strength in subjects with muscle wasting to improve their physical function.

    价 格：￥电议型 号：T3618产 地：中国大陆

  • T35878N-(3-Aminopropyl)cyclohexylamine

    N-(3-Aminopropyl)cyclohexylamine, a cyclohexylamine derivative, acts as a selective and competitive inhibitor of spermidine synthase. N-(3-Aminopropyl)cyclohexylamine can be used for the research of neurological diseases[1].

    价 格：￥电议型 号：T35878产 地：中国大陆

  • T3495TasimelteonVEC-162；BMS-214778；他司美琼

    Tasimelteon is a melatonin receptor agonist that is used for the treatment of non-24 hour sleep-wake disorder in blind individuals.

    价 格：￥电议型 号：T3495产 地：中国大陆

  • T3478Ro 67-7476

    Ro 67-7476 is a positive allosteric modulator of mGlu1 receptors. No activity at human mGlu1 receptors. Potentiates glutamate-induced calcium release with EC 50 of 60.1 nM.

    价 格：￥电议型 号：T3478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

  • T3378Alpha-Estradiolα-雌二醇；雌二醇；Epiestradiol；Epiestrol；17α-Estradiol；Alfatradiol

    Endogenous estrogen receptor ligand (Ki values are 0.2 and 1.2 nM for ERα and ERβ receptors respectively).

    价 格：￥电议型 号：T3378产 地：中国大陆

  • T3364Veratramine黎芦碱；藜芦胺；NSC23880；NSC17821

    Veratramine(NSC17821; NSC23880) is a potent signal transduction inhibitor for treating tumors.

    价 格：￥电议型 号：T3364产 地：中国大陆

  • T3336Rg3039PF-06687859

    RG3039 (PF-06687859) is a potent DcpS inhibitor. DcpS is a therapeutic target for spinal muscular atrophy. Spinal muscular atrophy (SMA) is caused by deletion or mutation of both copies of the SMN1 gene which produces an essential protein known as SMN. RG

    价 格：￥电议型 号：T3336产 地：中国大陆

  • T3278Piribedil吡贝地尔；EU-4200；Trivastan；Trivastal；ET-495

    Piribedil is a dopamine D2 agonist, used in the treatment of Parkinson´s disease.

    价 格：￥电议型 号：T3278产 地：中国大陆

  • T3182L-778123 hydrochlorideL 778123

    The L-778123 hydrochloride is an inhibitor of FPTase (IC50: 2 nM) and GGPTase-I (IC50: 98 nM) in enzyme inhibition determination.

    价 格：￥电议型 号：T3182产 地：中国大陆

  • T3078SGI-1776SGI-1776 free base；Pim-Kinase Inhibitor IX

    SGI-1776 has been used in trials studying the treatment of Prostate Cancer, Non-Hodgkins Lymphoma, and Relapsed/Refractory Leukemias.

    价 格：￥电议型 号：T3078产 地：中国大陆

  • T3046BMY 7378 dihydrochlorideBMY7378 HCl

    BMY-7378, α1D-adrenergic receptor antagonist, is a weak partial agonist/antagonist of 5-HT1A receptor.

    价 格：￥电议型 号：T3046产 地：中国大陆

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