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  • T4199Desmethyl-VS-5584

    Desmethyl-VS-5584 is a dimethyl analog of VS-5584, which is a novel and highly selective PI3K/mTOR kinase inhibitor for the treatment of cancer.

    价 格:¥电议型 号:T4199产 地:中国大陆

  • T4177U 19963

    U 19963 is an active compound.

    价 格:¥电议型 号:T4177产 地:中国大陆

  • T4119Octreotide AcetateSMS 201-995 (acetate);Sandostatin;Longastatin;SMS 201995;醋酸奥曲肽

    Octreotide acetate is a potent, long-acting synthetic somatostatin octapeptide analog that inhibits secretion of growth hormone.

    价 格:¥电议型 号:T4119产 地:中国大陆

  • T3199PTACHNCH-51;Cpd 51

    PTACH (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).

    价 格:¥电议型 号:T3199产 地:中国大陆

  • T3057UNC1999

    UNC1999 is a orally bioavailable, effective and specific inhibitor of EZH2 (IC50=2 nM) and EZH1 (IC50=45).

    价 格:¥电议型 号:T3057产 地:中国大陆

  • T2S1992Perillartine紫苏葶;DL-Perillartine;Perilla sugar;Peryllartine

    Perillartine is a sweetener, which activates the taste receptor type 1 member 2 (Tas1r2) subunit in a species-dependent manner.

    价 格:¥电议型 号:T2S1992产 地:中国大陆

  • T28199NS9283NS 9283;NS-9283

    NS9283, a positive allosteric modulator selective for the α4β2 form, reduces ethanol consumption.

    价 格:¥电议型 号:T28199产 地:中国大陆

  • T26375(S)-Amisulpride(S)-氨磺必利;SEP-4199;Esamisulpride

    (S)-Amisulpride (Esamisulpride) is a potent dopamine D2/D3 receptor antagonist. (S)-Amisulpride is an antagonist at the 5-HT7 receptor with a Ki of 900 nM. (S)-Amisulpride has antipsychotic and antidepressant effects.

    价 格:¥电议型 号:T26375产 地:中国大陆

  • T21995XAP044

    XAP044 is a mGlu7-selective antagonist which inhibits lateral amygdala long term potentiation (LTP) in brain slices from wild type mice with a half-maximal blockade at 88 nm[1].

    价 格:¥电议型 号:T21995产 地:中国大陆

  • T21992Vacuolin-1

    Vacuolin-1 is a cell-permeable inhibitor of Ca2+ dependent fusion of lysosomes to the cell membrane. It acts by inhibiting release of lysosomal content.vacuolin‐1 is a potent and selective PIKfyve inhibitor and inhibits late‐stage autophagy by impairing l

    价 格:¥电议型 号:T21992产 地:中国大陆

  • T2199Myclobutanil腈菌唑;Systhane

    Myclobutanil is a triazole chemical used as a fungicide. It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis. Ergosterol is a critical component of fungal cell membranes.

    价 格:¥电议型 号:T2199产 地:中国大陆

  • T2119Venetoclax维奈妥拉;ABT 199;ABT199;GDC-0199;ABT-199

    ABT-199 is a selective inhibitor of Bcl-2 (Ki < 0.010 nM), binding over 3 orders of magnitude less avidly to Bcl-xL, and Bcl-W (Kis = 48 and 245 nM, respectively).

    价 格:¥电议型 号:T2119产 地:中国大陆

  • T20166LDeltorphin acetateDeltorphin acetate(119975-64-3 Free base)

    Deltorphin acetate is a substance obtained from the skin secretions of a frog, Phyllomedusa bicolor and shows high selectivity and affinity for δ-opioid receptor.

    价 格:¥电议型 号:T20166L产 地:中国大陆

  • T199991-Tetralol, (S)-(S)-Tetralin-1-ol;J330.337C;(S)-1-Hydroxytetralin

    1-Tetralol, (S)- can be used as a substrate of AKR1C1 in cell assays.

    价 格:¥电议型 号:T19999产 地:中国大陆

  • T19991N-desmethylmirtazapine米氮平杂质D;J1.061.658A;ORG3838;Normirtazapine;ORG 3838;N-Demethylmirtazapine;ORG-3

    N-desmethylmirtazapine is a metabolite of mirtazapine. N-desmethylmirtazapine is also commonly used as an anxiolytic, hypnotic, antiemetic, and appetite stimulant.

    价 格:¥电议型 号:T19991产 地:中国大陆

  • T1999TaselisibRG-7604;GDC-0032

    Taselisib is an orally bioavailable inhibitor of the class I phosphatidylinositol 3-kinase (PI3K) alpha isoform (PIK3CA), with potential antineoplastic activity.

    价 格:¥电议型 号:T1999产 地:中国大陆

  • T19983Ethychlozate吲熟酯;IZAA;J 455;Etychlozate;BRN 0793218;Figaron

    Ethychlozate is a chemical agent that can accelerate coloration and enhance fruit quality.

    价 格:¥电议型 号:T19983产 地:中国大陆

  • T19982TralkoxydimTralkoxydime;Splendor

    Tralkoxydim is an alkyl ketone herbicide. Tralkoxydim works as an ACCase inhibitor.

    价 格:¥电议型 号:T19982产 地:中国大陆

  • T1998CHS-828GMX1778;CHS 828

    GMX1778(CHS-828), a pyridyl cyanoguanidine, is an effective inhibitor of NAD+ biosynthesis enzyme NAMPT (IC50 <25 nM).

    价 格:¥电议型 号:T1998产 地:中国大陆

  • T1997JNJ-31020028JNJ 31020028;JNJ31020028

    JNJ-31020028 is a selective brain penetrant antagonist of neuropeptide Y2 receptor with high affinity(pIC50=8.07, human; pIC50=8.22, rat); it exhibits >100-fold selectivity for Y2 versus human Y1/Y4/Y5 receptors.

    价 格:¥电议型 号:T1997产 地:中国大陆

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