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  • T71278IBPR002；化合物 IBPR002IBPR002

    IBPR002 is an aurora kinase inhibitor which reveals mechanisms of HURP in nucleation of centrosomal and kinetochore microtubules.

    价 格：￥电议型 号：T71278产 地：中国大陆

  • T71277Amiglumide；化合物 AmiglumideAmiglumide

    Amiglumide is a non-peptide cholecystokinin antagonist.

    价 格：￥电议型 号：T71277产 地：中国大陆

  • T71276MK-2748；化合物 MK-2748MK-2748

    MK-2748 is an inhibitor of NS3 protease, hepatitis C virus.

    价 格：￥电议型 号：T71276产 地：中国大陆

  • T71275CID16725315；化合物 CID16725315CID16725315

    Thiocarbazate, also known as CID16725315, is an inhibitor of human cathepsin L. Inhibition of cathepsin L thus holds promise for therapeutic intervention for both SARS-CoV and Ebola virus infection. With respect to the development of antiviral agents, inhibitors of human cathepsin L are not subject to resistance because of rapid mutations of the viral genome. Cathepsin L is therefore an attractive target for drug development.

    价 格：￥电议型 号：T71275产 地：中国大陆

  • T71274GLPG0259 A；化合物 GLPG0259 AGLPG0259 A

    GLPG0259 A is a small-molecule inhibitor of mitogen-activated protein kinase-activated protein kinase 5 (MAPKAPK5), a kinase enzyme that plays a role in important inflammatory pathways.

    价 格：￥电议型 号：T71274产 地：中国大陆

  • T71273CAY10788；化合物 CAY10788CAY10788

    CAY10788 is an antagonist of CysLT1 receptor.

    价 格：￥电议型 号：T71273产 地：中国大陆

  • T71272PI3K/Akt-IN-C89；化合物 PI3K/Akt-IN-C89PI3K/Akt-IN-C89

    PI3K/Akt-IN-C89 is a novel Inhibitor of the PI3K-Akt Pathway, Inducing Autophagy of Female Germline Stem Cells.

    价 格：￥电议型 号：T71272产 地：中国大陆

  • T71271RL71；化合物 RL71RL71

    RL71 is a sselective inhibitor of SERCA2, specially binding to SERCA2 at a novel site, suppressing the Ca2+-ATPase activity of SERCA2, inducing apoptosis and downregulating Akt.

    价 格：￥电议型 号：T71271产 地：中国大陆

  • T71270ZEL-H16；化合物 ZEL-H16ZEL-H16

    ZEL-H16 is an agonist of the histamine H3 receptor.

    价 格：￥电议型 号：T71270产 地：中国大陆

  • T7127DC260126；化合物DC260126DC260126

    DC260126 is a small-molecule antagonist of FFA1 (GPR40)

    价 格：￥电议型 号：T7127产 地：中国大陆

  • T71127Ipconazole [ISO]；化合物 Ipconazole [ISO]Ipconazole [ISO]

    Ipconazole is a member of the class of cyclopentanols carrying 1,2,4-triazol-1-ylmethyl, 4-chlorobenzyl and isopropyl substituents at positions 1, 2 and 5 respectively. Used to control a range of seed diseases in rice, vegetables and other, mainly non-food, crops. It has a role as an EC 1.14.13.70 (sterol 14alpha-demethylase) inhibitor and an antifungal agrochemical. It is a member of cyclopentanols, a member of monochlorobenzenes, a member of triazoles, a tertiary alcohol, a conazole fungicide

    价 格：￥电议型 号：T71127产 地：中国大陆

  • T70559GR-127935；化合物 GR-127935GR-127935

    GR-127935 is a potent and selective 5-HT1B/1D receptor antagonist.

    价 格：￥电议型 号：T70559产 地：中国大陆

  • T70334SRI-31277；化合物 SRI-31277SRI-31277

    SRI-31277 is a TSP1-TGFβ inhibitor.

    价 格：￥电议型 号：T70334产 地：中国大陆

  • T70127Famotine；化合物 FamotineFamotine

    Famotine is a histamine H2 receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease.

    价 格：￥电议型 号：T70127产 地：中国大陆

  • T6973RS-127445；化合物RS-127445MT500；MT500

    RS-127445 (MT500) is a selective 5-HT2B receptor antagonist with pKi of 9.5 and pIC50 of 10.4, exhibits >1000-fold selectivity against other 5-HT receptors.

    价 格：￥电议型 号：T6973产 地：中国大陆

  • T69127Moxisylyte；化合物 MoxisylyteMoxisylyte

    Moxisylyte, also known as thymoxamine, is a drug used in urology for the treatment of erectile dysfunction. It is an α1-adrenergic antagonist. Moxisylyte is also used for the short-term treatment of primary Reynaud´s syndrome, a condition where the fingers and toes become discoloured in response to cold or emotional distress. Moxisylyte helps by improving blood circulation to the extremities. It is also used locally in the eye to reverse the mydriasis caused by phenylephrine and other symp

    价 格：￥电议型 号：T69127产 地：中国大陆

  • T68913CCT068127；化合物 CCT068127CCT068127

    CCT068127 is a potent CDK2 and CDK9 inhibitor.

    价 格：￥电议型 号：T68913产 地：中国大陆

  • T68901SU11271；化合物 SU11271SU11271

    SU11271 is a potent c-MET inhibitor with potential anticancer activity.

    价 格：￥电议型 号：T68901产 地：中国大陆

  • T68758UNC10112785；化合物 UNC10112785UNC10112785

    UNC10112785 is a novel potent inhibitor of CDK8, CDK19, and CDK9 with IC50 at 1.05, 2.67, and 19.9 nM, respectively, causing MYC loss through both transcriptional and posttranslational mechanisms, and suppressing PDAC anchorage-dependent and anchorage-independent growth, inducing the substantial loss of MYC protein in both two-dimensional (2D) and 3D cell cultures.

    价 格：￥电议型 号：T68758产 地：中国大陆

  • T6837Flavopiridol；夫拉平度L868275|||Alvocidib|||NSC 649890 HCl|||HMR-1275；L868275|||Alvocidib|||夫拉平度|||NSC 64

    Flavopiridol (Alvocidib) (Alvocidib) competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1, 2, 4, 6 versus CDK7. Flavopiridol is initially found to inhibit EGFR and PKA. Phase 1/2.

    价 格：￥电议型 号：T6837产 地：中国大陆

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