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  • T16841SAR-260301

    SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM).

    价 格:¥电议型 号:T16841产 地:中国大陆

  • T1684Nitisinone尼替西农;NTBC;Nitisone;SC0735

    Nitisinone(SC0735) is an enzyme 4-hydroxyphenylpyruvate dioxygenase inhibitor.

    价 格:¥电议型 号:T1684产 地:中国大陆

  • T16684Puromycin aminonucleosideNSC 3056;维生素E醋酸酯

    Puromycin aminonucleoside increases podocyte permeability by modulating ZO-1 in an oxidative stress-dependent manner.

    价 格:¥电议型 号:T16684产 地:中国大陆

  • T11684Isoguvacine hydrochloride异四氢烟酸;1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride

    Isoguvacine hydrochloride is a GABA receptor agonist. Isoguvacine hydrochloride binds to rat synaptic cortical membranes and activates α1β2γ2S, α2β2γ2S, α3β2γ2S, α5β2γ2S, and ρ1 subunit GABAA receptors.

    价 格:¥电议型 号:T11684产 地:中国大陆

  • T0684RibavirinICN-1229;Tribavirin;NSC-163039;RTCA;利巴韦林

    Ribavirin is a synthetic nucleoside analog of ribofuranose with activity against hepatitis C virus and other RNA viruses.

    价 格:¥电议型 号:T0684产 地:中国大陆

  • T0684RibavirinRibavirin,ICN-1229,NSC-163039

    Ribavirin is a synthetic nucleoside analog of ribofuranose with activity against hepatitis C virus and other RNA viruses.

    价 格:¥电议型 号:T0684产 地:美洲

  • T11684Isoguvacine hydrochlorideIsoguvacine hydrochloride

    Isoguvacine hydrochloride is a GABA receptor agonist.

    价 格:¥电议型 号:T11684产 地:美洲

  • T12684Radioprotectin-1Radioprotectin-1

    Radioprotectin-1 is a potent and specific nonlipid lysophosphatidic acid receptor 2 (LPA2) agonist(murine LPA2 subtype with an EC50 value of 25 nM).

    价 格:¥电议型 号:T12684产 地:美洲

  • T16491PF-06446846 hydrochloridePF-06446846 hydrochloride

    PF-06446846 hydrochloride suppresses PCSK9 by inducing the ribosome to stall around codon 34. PF-06446846 hydrochloride is an orally active and highly selective inhibitor of translation of Proprotein convertase subtilisin/kexin type 9.

    价 格:¥电议型 号:T16491产 地:美洲

  • T16684Puromycin aminonucleosidePuromycin aminonucleoside,NSC 3056,

    Puromycin aminonucleoside is the aminonucleoside portion of the antibiotic puromycin. It is used in nephrosis animal models. Puromycin aminonucleoside also is a reversible inhibitor of dipeptidyl peptidase II and cytosol alanyl aminopeptidase. Puromycin a

    价 格:¥电议型 号:T16684产 地:美洲

  • T1684NitisinoneNitisinone,Nitisone,SC0735

    Nitisinone(SC0735) is an enzyme 4-hydroxyphenylpyruvate dioxygenase inhibitor.

    价 格:¥电议型 号:T1684产 地:美洲

  • T16841SAR-260301SAR-260301

    SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM).

    价 格:¥电议型 号:T16841产 地:美洲

  • T16842SaredutantSaredutant,SR 48968,SR 48968C

    Saredutant is an antagonist of selective NK2 receptors.

    价 格:¥电议型 号:T16842产 地:美洲

  • T16843SaridegibSaridegib,IPI-926,Patidegib

    Saridegib is an effective and specific inhibitor of Smoothened and a key signaling transmembrane protein in the Hedgehog pathway.

    价 格:¥电议型 号:T16843产 地:美洲

  • T16845SarolanerSarolaner,PF-6450567,

    Sarolaner is an orally active and broad-spectrum ectoparasiticide (LC80: 0.3 μg/mL against C. felis and an LC100: 0.003 μg/mL against O. turicata).

    价 格:¥电议型 号:T16845产 地:美洲

  • T16847SA 47SA 47

    SA 47 is a selective and effective inhibitor of fatty acid amide hydrolase and carbamate.

    价 格:¥电议型 号:T16847产 地:美洲

  • T16848SB-218078SB-218078

    SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 inhibitor that inhibits Chk1 phosphorylation of cdc25C (IC50: 15 nM).

    价 格:¥电议型 号:T16848产 地:美洲

  • T16849SB-222200SB-222200

    SB 222200 is a selective, reversible, and competitive antagonist of the human NK-3 receptor(Ki=4.4 nM).

    价 格:¥电议型 号:T16849产 地:美洲

  • T1851ZM 336372ZM 336372,Zinc00581684,

    ZM 336372 is a potent and selective c-Raf inhibitor.

    价 格:¥电议型 号:T1851产 地:美洲

  • T1852BelinostatBelinostat,NSC726630,PX-105684

    Belinostat is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibit

    价 格:¥电议型 号:T1852产 地:美洲

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