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  • TN7050Potassium 7-hydroxy-1-naphthalenesulfonaPotassium 7 hydroxy 1 naphthalenesulfona,Potassium 7hydroxy1

    Potassium 7-hydroxy-1-naphthalenesulfona is naturally present in the fruit of the Rubiaceae gardenia, the flowers of the Iridaceae crocus, and the flowers and leaves of the Scrophulariaceae Scrophulariaceae.

    价 格：￥电议型 号：TN7050产 地：中国大陆

  • T6517GolvatinibE7050,Golvatinib,c-Met/HGFR,VEGFR,Inhibitor,Vascular endothelial growth factor receptor,E

    Golvatinib is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050 binds to and inhibits the activities of both c-Met and VEGFR-2, which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of tumor cell types

    价 格：￥电议型 号：T6517产 地：中国大陆

  • T7050alpha-TocopherolquinonePhaeodactylum tricornutum,inhibit,vitamin K,α-Tocopherylquinone,alpha Tocophe

    During hypoxia in rats, levels of α-tocopherylquinon have been found to rise. It is reported to downregulate the respiratory activity of mitochondria. It has also displayed antioxidant activities after it is reduced to tocopherylhydroquinone.

    价 格：￥电议型 号：T7050产 地：中国大陆

  • T4637R-7050R7050；R 7050；TNF-α Antagonist III

    R-7050 is a tumor necrosis factor receptor (TNFR) antagonist with greater selectivity toward TNFα.

    价 格：￥电议型 号：T4637产 地：中国大陆

  • T4637R-7050R-7050,R7050,R 7050

    R-7050 is a tumor necrosis factor receptor (TNFR) antagonist with greater selectivity toward TNFα.

    价 格：￥电议型 号：T4637产 地：美洲

  • T6517GolvatinibGolvatinib,E-7050,

    Golvatinib is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050

    价 格：￥电议型 号：T6517产 地：美洲

  • T77050Laprituximab；化合物 LaprituximabLaprituximab

    Laprituximab (J2898A), a humanized IgG1 anti-EGFR antibody, is utilized in the synthesis of the antibody-drug conjugate (ADC) IMGN289 [1].

    价 格：￥电议型 号：T77050产 地：中国大陆

  • T70509INU-101；化合物 INU-101INU-101

    INU-101 is an 11β-HSD1 inhibitor. In KKAy mice, ob/ob mice, and ZDF rats, oral administration of INU-101 led to enhanced insulin sensitivity and the lowering of the fasting level of glucose in the blood. INU-101 therefore shows promise as a potential treatment for type 2 diabetes and metabolic syndrome.

    价 格：￥电议型 号：T70509产 地：中国大陆

  • T70507KAI-407；化合物 KAI-407KAI-407

    KAI407 is a potent non-8-aminoquinoline compound that kills Plasmodium cynomolgi early dormant liver stage parasites in vitro. KAI407 showed an activity profile similar to that of primaquine (PQ), efficiently killing the earliest stages of the parasites that become either primary hepatic schizonts or hypnozoites (50% inhibitory concentration [IC50] for hypnozoites, KAI407, 0.69 μM, and PQ, 0.84 μM; for developing liver stages, KAI407, 0.64 μM, and PQ, 0.37 μM). KAI407 may represent a new compou

    价 格：￥电议型 号：T70507产 地：中国大陆

  • T70506Bupranolol HCl；化合物 Bupranolol HClBupranolol HCl

    Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity. Its potency is similar to propranolol. Bupranolol is quickly and completely absorbed from the gut. Over 90% undergo first-pass metabolism. Bupranolol has a plasma half life of about two to four hours, with levels never reaching 1 ?g/l in therapeutic doses. The main metabolite is carboxybupranolol, 4-chloro-3-[3-(1,1-dimethylethylamino)-2-hydroxy-propyloxy]be

    价 格：￥电议型 号：T70506产 地：中国大陆

  • T70505Apaxifylline；化合物 ApaxifyllineApaxifylline

    Apaxifylline is a selective Adenosine A1 antagonist.

    价 格：￥电议型 号：T70505产 地：中国大陆

  • T705046,8-Diprenyleriodictyol；化合物 6,8-Diprenyleriodictyol6,8-Diprenyleriodictyol

    6,8-Diprenyleriodictyol is an antioxidant, which inhibits Cu(2+)-mediated oxidation of human low density lipoprotein (LDL).

    价 格：￥电议型 号：T70504产 地：中国大陆

  • T70503Exp 631；化合物 Exp 631Exp 631

    Exp 631 is a centrally-acting non-opioid analgesic; exhibits serotonin and norepinephrine reuptake inhibiting activities.

    价 格：￥电议型 号：T70503产 地：中国大陆

  • T70502AZ-27；化合物 AZ-27AZ-27

    AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.

    价 格：￥电议型 号：T70502产 地：中国大陆

  • T70501BDZ-h；化合物 BDZ-hBDZ-h

    BDZ-h is a potent inhibitor of both the closed-channel and the open-channel conformations of all four homomeric AMPA receptor channels and two GluA2R containing complex AMPA receptor channels.

    价 格：￥电议型 号：T70501产 地：中国大陆

  • T7050alpha-Tocopherolquinone托可醌托可醌|||Metarene

    During hypoxia in rats, levels of α-tocopherylquinon have been found to rise. alpha-Tocopherolquinone (Metarene) is reported to downregulate the respiratory activity of mitochondria. alpha-Tocopherolquinone has also displayed antioxidant activities after it is reduced to tocopherylhydroquinone.

    价 格：￥电议型 号：T7050产 地：中国大陆

  • T6517Golvatinib；戈伐替尼E-7050；E-7050|||戈伐替尼

    Golvatinib (E-7050) is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050 binds to and inhibits the activities of both c-Met and VEGFR-2, which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of tumor c

    价 格：￥电议型 号：T6517产 地：中国大陆

  • T4637R-7050；化合物R-7050TNF-α Antagonist III；TNF-α Antagonist III

    R-7050 (TNF-α Antagonist III), a tumor necrosis factor receptor (TNFR) antagonist, exhibits heightened selectivity for TNFα.

    价 格：￥电议型 号：T4637产 地：中国大陆

  • T37050MPS1/TTK Inhibitor；MPS1/TTK InhibitorMPS1/TTK Inhibitor；MPS1/TTK Inhibitor

    MPS1/TTK inhibitor is an inhibitor of monopolar spindle 1 (MPS1/TTK; IC50 = 5.8 nM), a kinase involved in mitotic spindle checkpoint signaling that is overexpressed in certain cancerous tumors. It inhibits MPS1 phosphorylation of kinetochore scaffold 1 (KNL1) and increases the rate of mitosis and the number of cells entering anaphase within 15 minutes, indicating MPS1 checkpoint inhibition, when used at a concentration of 100 nM. MPS1/TTK inhibitor (50 and 100 nM) increases the number of missegr

    价 格：￥电议型 号：T37050产 地：中国大陆

  • T28693SB-737050A；化合物 T28693SB 737050-A|||SB-737050-A|||SB737050-A；SB 737050-A|||SB-737050-A|||SB737050-A

    SB-737050A, a 5-HT antagonist, is used potentially for the treatment of schizophrenia.

    价 格：￥电议型 号：T28693产 地：中国大陆

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