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  • T16366NVR 3-778

    NVR 3-778 is a first-in-Class and oral bioavailable HBV CAM belonging to the SBA class It has anti-HBV activity.

    价 格:¥电议型 号:T16366产 地:中国大陆

  • T16355NSC781406

    NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).

    价 格:¥电议型 号:T16355产 地:中国大陆

  • T16350NSC-87877

    NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50=0.318 μM, 0.355 μM of shp2 and shp1, respectively).It also inhibits dual-specificity phosphatase 26 (DUSP26).

    价 格:¥电议型 号:T16350产 地:中国大陆

  • T1623Lopinavir洛匹那韦;ABT-378

    Lopinavir is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation. Lopinavir is less affected by binding to serum proteins than the structurally-related drug ritonavir.

    价 格:¥电议型 号:T1623产 地:中国大陆

  • T1617Enrofloxacin恩诺沙星;PD160788;BAY-Vp2674

    Enrofloxacin is a veterinary antibacterial agent, used in poultry.

    价 格:¥电议型 号:T1617产 地:中国大陆

  • T16156MT 63-78

    MT 63-78 is a specific and effective direct AMPK activator (EC50: 25 μM). MT 63-78 blocks prostate cancer growth by inhibiting the lipogenesis and mTORC1 pathways. MT 63-78 has antitumor effects. MT 63–78 also causes cell mitotic arrest and apoptosis.

    价 格:¥电议型 号:T16156产 地:中国大陆

  • T16153MS4078

    MS4078 is an inhibitor and aplastic lymphoma kinase (ALK) PROTAC (degrader) based on Cereblon ligand, with a Kd of 19?nM for binding affinity to ALK.

    价 格:¥电议型 号:T16153产 地:中国大陆

  • T16018MB-07811VK-2809

    MB-07811 is an orally active HepDirect prodrug of MB07344 and is a liver-targeted thyroid hormone receptor-β agonist. MB-07811 has cholesterol and triglycerides lowering activity.

    价 格:¥电议型 号:T16018产 地:中国大陆

  • T15789LTURM34

    LTURM34 is an inhibitor of DNA-PK with IC50 of 34 nM. LTURM34 displays effective antiproliferative activity in a wide range of tumor cell lines. LTURM34 shows 170-fold selectivity for DNA-PK over PI3K .

    价 格:¥电议型 号:T15789产 地:中国大陆

  • T15784LP99

    LP99 is an epigenetic probe. LP99 disrupts the binding of BRD7 and BRD9 to chromatin in cells. LP99 is an effective and selective inhibitor of the BRD7 and BRD9 bromodomains (Kd: 99 nM against BRD9).

    价 格:¥电议型 号:T15784产 地:中国大陆

  • T15782Lp-PLA2-IN-1Lp-PLA2 inhibitor 1;Lp-PLA2 -IN-1

    Lp-PLA2 -IN-1 suppresses Lp-PLA2 activity processes for their preparation. Lp-PLA2 -IN-1also inhibits to compositions containing them and to their use in the treatment of diseases associated with the activity of Lp-PLA2, for example, atherosclerosis, Alzh

    价 格:¥电议型 号:T15782产 地:中国大陆

  • T15781LP-935509

    LP-935509 is highly brain-penetrant and reverses fully established pain behavior following the SNL procedure. LP-935509 is an effective inhibitor of BIKE (IC50=14 nM) and a modest inhibitor of cyclin G-associated kinase(GAK, IC50=320 nM). LP-935509 is als

    价 格:¥电议型 号:T15781产 地:中国大陆

  • T1578Pargyline hydrochloridePargylamine hydrochloride;优降宁盐酸盐

    Pargyline hydrochloride is an irreversible monoamine oxidase(MAO) inhibitor with antihypertensive properties.

    价 格:¥电议型 号:T1578产 地:中国大陆

  • T15624JNJ-64619178

    JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.

    价 格:¥电议型 号:T15624产 地:中国大陆

  • T15578IndotecanNSC-724998;LMP-400

    Indotecan is an effective inhibitor of topoisomerase 1(Top1) (IC50: 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively).

    价 格:¥电议型 号:T15578产 地:中国大陆

  • T1546Nitazoxanide硝唑尼特;NSC 697855

    Nitazoxanide is a synthetic benzamide with antiprotozoal activity. Nitazoxanide exerts its antiprotozoal activity by interfering with the pyruvate ferredoxin/flavodoxin oxidoreductase dependent electron transfer reaction.

    价 格:¥电议型 号:T1546产 地:中国大陆

  • T15435GSK2837808A

    GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).

    价 格:¥电议型 号:T15435产 地:中国大陆

  • T15405GNE-781

    GNE-781 is a highly potent and selective inhibitor of CBP (IC50: 0.94 nM in TR-FRET assay). GNE-781 also inhibits BRET and BRD4(1) (IC50s: 6.2 nM and 5100 nM, respectively).

    价 格:¥电议型 号:T15405产 地:中国大陆

  • T15278FezolinetantESN-364

    Fezolinetant is an antagonist of the neurokinin 3 receptor (NK3R). It is used for the treatment of menopausal hot flushes.

    价 格:¥电议型 号:T15278产 地:中国大陆

  • T14978CL-82198

    CL-82198 is a selective inhibitor of MMP-13 and it is a pharmacologic treatment for preventing osteoarthritis (OA) progression. CL-82198 binds to the entire S1’ pocket of MMP-13, which is the basis for its selectivity towards MMP-13 and the lack of inhibi

    价 格:¥电议型 号:T14978产 地:中国大陆

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