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  • T3762Hyaluronic acid透明质酸；玻尿酸；hyaluronan；Hyaluronate

    Hyaluronic Acid is a glucosaminoglycan consisting of D-glucuronic acid and N-acetyl-D-glucosamine disaccharide units that is a component of connective tissue, skin, vitreous humour, umbilical cord, synovial fluid and the capsule of certain microorganisms

    价 格：￥电议型 号：T3762产 地：中国大陆

  • T37611-OctacosanolOctacosanol；Montanyl alcohol；Octanosol；n-Octacosanol；Octacosyl alcohol；Cluytyl alcohol；

    1-Octacosanol is a straight-chain aliphatic 28-carbon primary fatty alcohol that is used as a nutritional supplement. It is reported to possess cholesterol-lowering effects, antiaggregatory properties, cytoprotective use, and ergogenic properties.

    价 格：￥电议型 号：T3761产 地：中国大陆

  • T37603LOsteogenic Growth Peptide (10-14) acetateOsteogenic Growth Peptide (10-14) acetate(105250-85-9 Free

    Osteogenic Growth Peptide (10-14) acetate is a Src inhibitor and an effective mitogen and stimulator of osteogenesis and hematopoiesis. Osteogenic Growth Peptide (10-14) acetate is responsible for the binding to the OGP receptor and activates an intracell

    价 格：￥电议型 号：T37603L产 地：中国大陆

  • T37600Dasatinib N-oxide

    Dasatinib N-oxide is a major metabolite of the Abl and Src kinase inhibitor dasatinib.It is also a potential impurity in commercial preparations of dasatinib[1][2].

    价 格：￥电议型 号：T37600产 地：中国大陆

  • T3713BAY-876BAY 876；BAY876

    BAY-876 is a potent and selective GLUT1 inhibitor.

    价 格：￥电议型 号：T3713产 地：中国大陆

  • T3705GDC0084RG7666；GDC-0084；GDC 0084

    GDC-0084 (RG7666) is a PI3K inhibitor with potential antineoplastic activity. GDC-0084 specifically inhibits PI3K in the PI3K/AKT kinase (or protein kinase B) signaling pathway, thereby inhibiting the activation of the PI3K signaling pathway. This may res

    价 格：￥电议型 号：T3705产 地：中国大陆

  • T3700SCH900776 (S-isomer)MK-8776 S-isomer；SCH900776 S-isomer

    SCH900776 (S-isomer) is an effective, specific and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50: 3 nM). It also inhibitors Chk2 (IC50: 1500 nM) and cyclin-dependent kinase CDK2 (IC50: 160 nM).

    价 格：￥电议型 号：T3700产 地：中国大陆

  • T3676Sesamol芝麻酚；1,3-Benzodioxol-5-ol；3,4-Methylenedioxyphenol

    Sesamol could decrease lung inflammation and lipopolysaccharide (LPS)-induced lung injury in rats. Sesamol ameliorates inflammatory and oxidative damage by upregulating AMPK activation and Nrf2 signaling and blocking the NF-κB and MAPK signaling pathways

    价 格：￥电议型 号：T3676产 地：中国大陆

  • T3643HMN-176HMN 176；HMN176

    HMN-176 is a stilbene derivative which inhibits mitosis, interfering with polo-like kinase-1 (plk1).

    价 格：￥电议型 号：T3643产 地：中国大陆

  • T35856BMS-986176

    AAK1-IN-1 is a highly selective and potent inhibitor of adaptor associated kinase 1 (AAK1, IC50 = 2 nM).

    价 格：￥电议型 号：T35856产 地：中国大陆

  • T3581KS176

    KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BCRP) multidrug transporter, showing no inhibitory activity against P-gp or MRP1.

    价 格：￥电议型 号：T3581产 地：中国大陆

  • T3576KDM5-inhibitorCPI-455 analogue

    KDM5 inhibitor

    价 格：￥电议型 号：T3576产 地：中国大陆

  • T3550X-376X-396；Ensartinib；恩沙替尼

    Ensartinib (X-396) is an orally available small molecule inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with potential antineoplastic activity. Upon oral administration, X-396 binds to and inhibits ALK kinase, ALK fusion protei

    价 格：￥电议型 号：T3550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

  • 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

  • T3476JI-101JI 101；JI101；CGI-1842

    JI-101 is an oral multi-kinase inhibitor that targets vascular endothelial growth factor receptor type 2 (VEGFR-2), platelet derived growth factor receptor β (PDGFR-β), and ephrin type-B receptor 4 (EphB4).

    价 格：￥电议型 号：T3476产 地：中国大陆

  • T3435Vicriviroc maleateSCH-D (maleate)；SCH-417690 (maleate)；维立韦罗马来酸盐

    Vicriviroc maleate(Sch-417690) is a piperazine-based CCR5 receptor antagonist with activity against human immunodeficiency virus. The IC50 value is 0.91 nM in clinical development for the treatment of HIV-1.

    价 格：￥电议型 号：T3435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

  • T3403Glabridin光甘草定；Q-100692；KB-289522；LS-176045

    Glabridin may serve as an anti-inflammatory agent in diabetes-related vascular dysfunction, through regulating the synthesis and activity of iNOS under high-glucose levels; may possess a therapeutic effect on metabolic disorders( such as diabetes and hype

    价 格：￥电议型 号：T3403产 地：中国大陆

  • T33762Fosifloxuridine nafalbenamideNUC-3373；NUC 3373；NUC3373

    NUC-3373 (Fosifloxuridine nafalbenamide), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor.NUC-3373 has anticancer activity. NUC-3373 is a ProTide transformation of 5-FU that generates much higher concentrations of FUDR-MP in patients

    价 格：￥电议型 号：T33762产 地：中国大陆

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