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  • T2669BerzosertibVX-970;VE-822

    VE-822 has been used in trials studying the treatment of Ovarian Neoplasms, Ovarian Serous Tumor, Adult Solid Neoplasm, Advanced Solid Tumor, and Advanced Solid Neoplasm, among others.

    价 格:¥电议型 号:T2669产 地:中国大陆

  • T2618LGK974LGK 974;WNT974;LGK-974;NVP-LGK974

    LGK-974 is an effective and selective PORCN inhibitor and inhibits Wnt signaling (IC50: 0.4 nM) in TM3 cells. It has been used in trials studying the treatment of Metastatic Colorectal Cancer and Squamous Cell Carcinoma, Head And Neck.

    价 格:¥电议型 号:T2618产 地:中国大陆

  • T2597Norgestrel甲基炔诺酮;炔诺孕酮;SH-850;WY-3707;SH-70850;FH 122-A

    Norgestrel is a synthetic progestin commonly used alone or in combination with an estrogen for contraception. Norgestrel suppresses the secretion of luteinizing and follicle-stimulating hormones (LH and FSH), thickens cervical mucus, and slows the transit

    价 格:¥电议型 号:T2597产 地:中国大陆

  • T2562Eltrombopag艾曲波帕;SB-497115-GR;SB-497115

    Eltrombopag, an orally active thrombopoietin receptor agonist with megakaryopoiesis stimulating activity, binds to and stimulates the platelet thrombopoietin receptor (TPO-R or CD110).

    价 格:¥电议型 号:T2562产 地:中国大陆

  • T249774-Isopropoxybenzoic acidAI3 12104;AI3-12104;AI312104;4-异丙氧苯甲酸

    4-Isopropoxybenzoic acid is a Centromere-Associated Protein E inhibitor.

    价 格:¥电议型 号:T24977产 地:中国大陆

  • T2497MPEP hydrochloride

    MPEP hydrochloride is an effective and highly specific non-competitive antagonist at the mGlu5 receptor subtype (IC50: 36 nM).

    价 格:¥电议型 号:T2497产 地:中国大陆

  • T2494CilengitideEMD 121974;西仑吉肽

    Cilengitide is a potent integrin inhibitor for the αvβ3/5 receptor (IC50: 4.1/79 nM, in cell-free assays); ~10-fold selectivity against gpIIbIIIa.

    价 格:¥电议型 号:T2494产 地:中国大陆

  • T24897TP0427736TP427736;TP-0427736;TP-427736

    TP0427736 is a potent and selective inhibitor of ALK5 with an IC50 of 2.72 nM, 300-fold higher than the inhibitory effect on ALK3. TP0427736 reduces TGF-β-induced growth inhibition in human outer root sheath cells and elongates the anagen phase in mouse h

    价 格:¥电议型 号:T24897产 地:中国大陆

  • T24697LR 396 acetate

    R 396 acetate is an NK-2 Tachykinin Receptor $nAntagonist.

    价 格:¥电议型 号:T24697L产 地:中国大陆

  • T2464NSC319726ZMC1

    NSC319726, a mutant p53R175 reactivator, suppresses growth of fibroblasts that expresses the p53R175 mutation (IC50 = 8 nM).

    价 格:¥电议型 号:T2464产 地:中国大陆

  • T2397TopiroxostatFYX-051;托匹司他

    Topiroxostat is a selective xanthine oxidase inhibitor developed for treatment and management of hyperuricemia and gout.

    价 格:¥电议型 号:T2397产 地:中国大陆

  • T23087NPY 5RA972

    NPY 5RA972 is a neuropeptide Y Y5 receptor antagonist

    价 格:¥电议型 号:T23087产 地:中国大陆

  • T22976MFZ 10-7

    MFZ 10-7 is anegative allosteric modulator of the mGluR5. In rats, MFZ 10-7 (i.p.) inhibits cocaine-induced reinstatement of drug-seeking behavior, cocaine-associated cue-induced cocaine-seeking behavior and intravenous cocaine self-administration.

    价 格:¥电议型 号:T22976产 地:中国大陆

  • T22974Methyl 2,5-dihydroxycinnamate

    Methyl 2,5-dihydroxycinnamate is an EGF receptor-associated tyrosine kinases inhibitor.

    价 格:¥电议型 号:T22974产 地:中国大陆

  • T2297PIK-294PIK294;PIK 294

    PIK-294 is a excellently specific p110δ inhibitor(IC50=10 nM).

    价 格:¥电议型 号:T2297产 地:中国大陆

  • T22851ICI 63197三氮唑嘧啶酮;2-Amino-6-methyl-4-propyl-[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one

    ICI 63197 is a PDE4 inhibitor.

    价 格:¥电议型 号:T22851产 地:中国大陆

  • T2272BPR1J-097BPR1J097;BPR1J 097

    BPR1J-097 is a novel FLT-3 inhibitor(IC50: 11±7 nM) with promising in vivo anti-tumor activities. It also inhibits FLT-3 D835Y (IC50: 3 nM).

    价 格:¥电议型 号:T2272产 地:中国大陆

  • T22697CS 21001-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxy

    CS 2100 is an S1P1 agonist.

    价 格:¥电议型 号:T22697产 地:中国大陆

  • T2268VER49009VER 49009;CCT0129397;VER-49009

    VER-49009 is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).

    价 格:¥电议型 号:T2268产 地:中国大陆

  • T22665PD 128042CI 976

    CI 976 is a potent orally active and selective ACAT inhibitor(IC50: 73 nM) and a potent lysophospholipid acyltransferase(LPAT) inhibitor. CI 976 inhibits Golgi-associated LPAT activity (IC50: 15 μM) and multiple membrane trafficking steps.

    价 格:¥电议型 号:T22665产 地:中国大陆

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