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  • T16670PS210

    PS210 is inactive against other protein kinases, including PDK1 downstream signaling components such as S6K, PKB/Akt, or GSK3. PS210 is a potent and selective PDK1 activator (Kd: 3 μM) and targets the PIF-binding pocket of PDK1. In cells, the prodrug of P

    价 格：￥电议型 号：T16670产 地：中国大陆

  • T1667Tandutinib坦度替尼；NSC726292；CT53518；MLN518

    Tandutinib (MLN518, CT53518), an effective FLT3 antagonist (IC50: 0.22 μM), can also inhibit c-Kit and PDGFR, 15-20 fold higher potency for FLT3 versus CSF-1R and >100-fold selectivity for the same target versus FGFR, EGFR, and KDR.

    价 格：￥电议型 号：T1667产 地：中国大陆

  • T14667BLT-1

    BLT-1 is a scavenger receptor BI (SR-BI)inhibitor.

    价 格：￥电议型 号：T14667产 地：中国大陆

  • T13398ZINC13466751

    ZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 ?M).

    价 格：￥电议型 号：T13398产 地：中国大陆

  • T10667Calmidazolium chlorideR 24571；钙调蛋白抑制剂

    Calmidazolium chloride is a calmodulin (CaMK) antagonist (Kd = 3 nM), antagonizing CaM-dependent phosphodiesterase(IC50 = 0.15 μM) and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase(IC50 = 0.35 μM). Calmidazolium chloride also induc

    价 格：￥电议型 号：T10667产 地：中国大陆

  • T0907SulfasalazineNSC 667219；Azulfidine；柳氮磺吡啶

    Sulfasalazine is a synthetic salicylic acid derivative with affinity for connective tissues containing elastin and formulated as a prodrug

    价 格：￥电议型 号：T0907产 地：中国大陆

  • T0667Flecainide Impurity D

    Flecainide Impurity D is used as an intermediate in industry.

    价 格：￥电议型 号：T0667产 地：中国大陆

  • T0667Flecainide Impurity DFlecainide Impurity D

    Flecainide Impurity D is used as an intermediate in industry.

    价 格：￥电议型 号：T0667产 地：美洲

  • T0907SulfasalazineSulfasalazine,NSC 667219,Azulfidine

    Sulfasalazine is a synthetic salicylic acid derivative with affinity for connective tissues containing elastin and formulated as a prodrug

    价 格：￥电议型 号：T0907产 地：美洲

  • T10667Calmidazolium chlorideCalmidazolium chloride,R 24571,

    Calmidazolium chloride (R 24571) is a calmodulin (CaMK) antagonist (Kd: 3 nM), antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase (IC50s: 0.15 and 0.35 μM).

    价 格：￥电议型 号：T10667产 地：美洲

  • T10823cis-Pralsetinibcis-Pralsetinib,cis-BLU-667,

    trans-Pralsetinib (trans-BLU-667) is an inhibitor of rearranged during transfection (RET) extracted from patent US20170121312A1 (Compound Example 129).

    价 格：￥电议型 号：T10823产 地：美洲

  • T12647(R)-VU 6008667(R)-VU 6008667

    (R)-VU 6008667 is devoid of M5 NAM activity (IC50>10 μM).

    价 格：￥电议型 号：T12647产 地：美洲

  • T12679(Rac)-VU 6008667(Rac)-VU 6008667

    (Rac)-VU 6008667 is a selective negative allosteric modulator of muscarinic acetylcholine receptor subtype 5 (M5 NAM) with IC50 of 1.8 μM and pIC50 of 5.75, has high CNS penetration.

    价 格：￥电议型 号：T12679产 地：美洲

  • T16430PalirodenPaliroden,SR 57667,

    Paliroden is an orally bioactive neurotrophic, non-peptidic compound that activates the synthesis of endogenous neurotrophines. It is used for the treatment of Alzheimer´s Disease and Parkinson´s.

    价 格：￥电议型 号：T16430产 地：美洲

  • T1667TandutinibTandutinib,CT53518,MLN518

    Tandutinib (MLN518, CT53518), an effective FLT3 antagonist (IC50: 0.22 μM), can also inhibit c-Kit and PDGFR, 15-20 fold higher potency for FLT3 versus CSF-1R and >100-fold selectivity for the same target versus FGFR, EGFR, and KDR.

    价 格：￥电议型 号：T1667产 地：美洲

  • T16673PseudouridimycinPseudouridimycin,PUM,

    Pseudouridimycin is a C-nucleoside analogue. Pseudouridimycin is an antibiotic and is a selective bacterial RNA polymerase (RNAP) inhibitor. It is effective against both Gram-negative and Gram-positive bacteria.

    价 格：￥电议型 号：T16673产 地：美洲

  • T16674PseudouridinePseudouridine

    Pseudouridine is the most abundant modified nucleoside in non-coding RNAs. It enhances the function of transfer RNA and ribosomal RNA by stabilizing RNA structure.

    价 格：￥电议型 号：T16674产 地：美洲

  • T16676PSI-697PSI-697,P-Selectin Inhibitor,

    PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).

    价 格：￥电议型 号：T16676产 地：美洲

  • T16677PsicofuraninePsicofuranine

    Psicofuranine also specifically inhibits GMP synthase and interrupts parasite growth. Psicofuramine is a nucleoside antibiotic. It has the inhibition of xanthosine 5´-phosphate aminase. Psicofuranine shows dose-dependent inhibition of P. falciparum growth

    价 格：￥电议型 号：T16677产 地：美洲

  • T16678PSN632408PSN632408

    PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).

    价 格：￥电议型 号：T16678产 地：美洲

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