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  • T21919UCF 101

    UCF 101 is a specific inhibitor of HtrA2 and reduces apoptosis in PC12 cells.

    价 格：￥电议型 号：T21919产 地：中国大陆

  • T21314AmsilaroteneTAC-101；TAC 101；TAC101

    Amsilarotene inhibits the phosphorylation of retinoblastoma gene product (RB) and increases the presence of 2 cyclin-dependent kinases (CDK) inhibitors resulting in cell cycle arrest. This agent also causes a cytotoxic decline in the thymidylate synthase

    价 格：￥电议型 号：T21314产 地：中国大陆

  • T2120I-BET151GSK1210151A

    I-BET151 (GSK1210151A) is a specific BET inhibitor for BRD2/3/4 (IC50: 0.5/0.25/0.79 μM, in cell-free assays).

    价 格：￥电议型 号：T2120产 地：中国大陆

  • T21013Clomipramine氯米帕明；Anafranil (free base)；Clomicalm；Clomipramina；Chlorimipramine；Anafranil

    Clomipramine is a tricyclic antidepressant (TCA). It is used for the treatment of the panic disorder, obsessive-compulsive disorder, major depressive disorder, and chronic pain. It may decrease the risk of suicide in those over the age of 65. It is simila

    价 格：￥电议型 号：T21013产 地：中国大陆

  • T21011BuspironeAnsial

    Buspirone free base is an agonist of serotonin receptor with anxiolytic activity. Buspirone free base has an efficacy comparable to diazepam.

    价 格：￥电议型 号：T21011产 地：中国大陆

  • T2101NavitoclaxABT-263

    Navitoclax (ABT-263) is a potent, orally bioavailable Bcl-2 family protein inhibitor that avidly binds Bcl-2, Bcl-xL, and Bcl-W (Ki < 1 nM for all three proteins).

    价 格：￥电议型 号：T2101产 地：中国大陆

  • T2008LY294002NSC 697286；SF 1101；LY 294002

    LY294002 is an inhibitor of PI3K (IC50s: 0.5/0.57/0.97 μM for PI3Kα/δ/β in cell-free assays). It also blocks autophagosome formation.

    价 格：￥电议型 号：T2008产 地：中国大陆

  • T20076Irganox 1010Dovernox 10

    Irganox 1010 is an agent of antioxidant.

    价 格：￥电议型 号：T20076产 地：中国大陆

  • T1995FedratinibSAR 302503；TG-101348

    Fedratinib (TG101348) is an ATP-competitive inhibitor of JAK2 (IC50: 3 nM) with significantly less potent activity against JAK3.

    价 格：￥电议型 号：T1995产 地：中国大陆

  • T1911AfuresertibGSK2110183C；GSK2110183

    Afuresertib is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity.

    价 格：￥电议型 号：T1911产 地：中国大陆

  • T19062Sulforhodamine 101磺基罗丹明101；磺基罗丹明 101；SR101

    Sulforhodamine 101 is a red fluorescent dye.

    价 格：￥电议型 号：T19062产 地：中国大陆

  • T1894IdelalisibCAL-101；GS-1101；艾代拉里斯

    Idelalisib is a small molecule inhibitor of the PI3K catalytic subunit p110δ (IC50: 2.5 nM). The selectivity for p110δ is 40- to 300-fold than p110α/β/γ.

    价 格：￥电议型 号：T1894产 地：中国大陆

  • T1852BelinostatNSC726630；PXD101；PX-105684

    Belinostat is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibit

    价 格：￥电议型 号：T1852产 地：中国大陆

  • T17877VH032-cyclopropane-FPhenolic VH101；VHL ligand 3；E3 ligase Ligand 19

    VH032-cyclopropane-F is a VH032-based VHL ligand. VH032-cyclopropane-F can be connected to the ligand for protein by a linker to form PROTACs. PROTAC 1 is a partial degrader of SMARCA2 and SMARCA4.

    价 格：￥电议型 号：T17877产 地：中国大陆

  • T1774IntepirdineSB 742457；GSK-742457；RVT-101

    SB742457 is a highly selective 5-HT6 receptor antagonist, used in trials studying the treatment of Alzheimer´s Disease.

    价 格：￥电议型 号：T1774产 地：中国大陆

  • T15616JNJ-10198409JNJ-?10198409；3-氟-N-(6,7-二甲氧基-2,4-二氢茚并[1,2-C〕吡唑-3-基苯基胺

    JNJ- 10198409 is a relatively selective and ATP competitive PDGF-RTK inhibitor (IC50=2 nM). JNJ-10198409 has good activity against PDGFR-β kinase (IC50=4.2 nM) and PDGFR-α kinase (IC50=45 nM). It is a dual-mechanism, antiangiogenic, and tumor cell antipro

    价 格：￥电议型 号：T15616产 地：中国大陆

  • T15034RoluperidoneMT-210；CYR-101；MIN-101

    Roluperidone is a novel cyclic amide derivative. It has high equipotent affinities for 5-HT2A and σ2 receptors (Ki of 7.53 nM and 8.19 nM for 5-HT2A and σ2).

    价 格：￥电议型 号：T15034产 地：中国大陆

  • T14989CMPD101

    CMPD101 is a membrane-permeable small-molecule inhibitor of GRK2/3 (IC50: 18 nM and 5.4 nM). Which can be used for the study of heart failure. CMPD101 exhibits less selectively against GRK1, GRK5, ROCK-2 and PKCα with IC50s of 3.1 μM , 2.3 μM, 1.4 μM and

    价 格：￥电议型 号：T14989产 地：中国大陆

  • T1447Fenclonine芬克洛宁；CP-10188；PCPA；4-Chloro-DL-phenylalanine；Fenchlonine；DL-4-Chlorophenylalanine

    Fenclonine is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine acts pharmacologically to deplete endogenous levels of serotonin.

    价 格：￥电议型 号：T1447产 地：中国大陆

  • T14133AEOL-10150 pentachloride

    AEOL-10150 pentachloride is a metalloporphyrin catalytic antioxidant. AEOL-10150 pentachloride also is a superoxide dismutase mimetic. Which protects lungs from radiation-induced injury.

    价 格：￥电议型 号：T14133产 地：中国大陆

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