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  • T15432GSK256073

    GSK256073 is an orally active GPR109A agonist. GSK256073 also is a long-lasting and non-flushing HCA2 (hydroxy-carboxylic acid receptor 2) full agonist (pEC50: 7.5). GSK256073 acutely improves glucose homeostasis via inhibition of lipolysis.

    价 格:¥电议型 号:T15432产 地:中国大陆

  • T15430GSK2256294AGSK 2256294

    GSK2256294A is potent, selective inhibitor of recombinant human, rat and mouse sEH with IC50 of 27 pM, 61 pM and 189 pM, respectively.

    价 格:¥电议型 号:T15430产 地:中国大陆

  • T1543Naftifine hydrochloride盐酸萘替芬;Exoderil;Naftifungin;Naftin;Naftifine HCl

    Naftifine Hydrochloride is the hydrochloride salt form of naftifine, an allylamine derivate with synthetic broad-spectrum antifungal activity. Although the exact mechanism through which naftifine hydrochloride exerts its effect is unknown, it appears to s

    价 格:¥电议型 号:T1543产 地:中国大陆

  • T15427GSK2033

    GSK2033 is an antagonist of LXR (pIC50s: 7 and 7.4 for LXRα or LXRβ, respectively).

    价 格:¥电议型 号:T15427产 地:中国大陆

  • T15424GSK1379725A

    GSK1379725A is a selective BPTF ligand (Kd = 2.8 μM).

    价 格:¥电议型 号:T15424产 地:中国大陆

  • T15422GSK-626616

    GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50: 0.7 nM). It inhibits other members of the DYRK family with similar potency. GSK-626616 is a potential therapy for the treatment of anemia.

    价 格:¥电议型 号:T15422产 地:中国大陆

  • T1542Pirenzepine dihydrochloride盐酸哌仑西平;Bisvanil;LS519;Pirenzepine HCl;Tabe

    Pirenzepine dihydrochloride is a selective M1 muscarinic receptor antagonist, inhibiting gastric secretion.

    价 格:¥电议型 号:T1542产 地:中国大陆

  • T15418GS-6201CVT-6883

    GS-6201 is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors with a Ki of 22 nM.

    价 格:¥电议型 号:T15418产 地:中国大陆

  • T15416GR148672X4,4,4-三氟-1-(2-噻吩基)-1,2,3-丁三酮 2-[(3-甲基苯基)腙]

    GR148672X is an inhibitor of triacyglycerol hydrolase (TGH) (IC50: 4 nM).

    价 格:¥电议型 号:T15416产 地:中国大陆

  • T15413GPR120 Agonist 3GPR120-IN-1

    GPR120-IN-1 is a selective agonist of Gpr120 ( logEC50: -7.62).

    价 格:¥电议型 号:T15413产 地:中国大陆

  • T15411GPNA hydrochloride

    GPNA hydrochloride is specific glutamine (Gln) transporter ASCT2(SLC1A5) inhibitor. GPNA reversibly induces apoptosis in A549 cells. GPNA hydrochloride is a well-known substrate of the enzyme γ-glutamyltransferase (GGT). GPNA hydrochloride also inhibits

    价 格:¥电议型 号:T15411产 地:中国大陆

  • T15410GNF351

    GNF351 is a full antagonist of the aryl hydrocarbon receptor (AHR)with the capacity to inhibit both DRE-dependent and -independent activity. GNF351 is minimal toxicity in mouse or human keratinocytes. GNF351 competes with a photoaffinity AHR ligand for bi

    价 格:¥电议型 号:T15410产 地:中国大陆

  • T1541DrospirenoneDihydrospirorenone;ZK 3059;屈螺酮

    Drospirenone is a synthetic spironolactone analogue and progestin with progestational and anti-mineralocorticoid activity.

    价 格:¥电议型 号:T1541产 地:中国大陆

  • T15409GNF179

    GNF179 is an optimized 8,8-dimethyl IP analog. It exhibited the potency(4.8 nM against the multidrug resistant strain W2) in vitro metabolic stability and in vivo oral bioavailability.

    价 格:¥电议型 号:T15409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

  • T1540Doxepin hydrochlorideDoxepin HCl;Novoxapin;Toruan;Aponal;盐酸多塞平

    Doxepin Hydrochloride is a dibenzoxepin tricyclic compound. It displays a range of pharmacological actions including maintaining adrenergic innervation. Its mechanism of action is not fully understood, but it appears to block reuptake of monoaminergic neu

    价 格:¥电议型 号:T1540产 地:中国大陆

  • T14907CCT251545

    CCT251545 is an potent and oral-bioavailable WNT signaling inhibitor(IC50 of 5 nM in 7dF3 cells).

    价 格:¥电议型 号:T14907产 地:中国大陆

  • T12154LN-Desethyl amodiaquine dihydrochloride

    N-Desethyl amodiaquine dihydrochloride is an antiparasitic agent,is the major biologically active Amodiaquine metabolite .

    价 格:¥电议型 号:T12154L产 地:中国大陆

  • T11657INH154

    INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.

    价 格:¥电议型 号:T11657产 地:中国大陆

  • T11546hDHODH-IN-1

    hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.

    价 格:¥电议型 号:T11546产 地:中国大陆

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