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T8405Vardenafil hydrochloridePDE-5 inhibitors,Vardenafil,Endogenous Metabolite,diabetes,Zucker diabetic f
Vardenafil hydrochloride is a New Phosphodiesterase Type 5(PDE5) Inhibitor, in the Treatment of Erectile Dysfunction in Men With Diabetes
价 格：￥电议型 号：T8405产 地：中国大陆
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T4692Protein kinase inhibitors 1 hydrochloridProtein kinase inhibitors 1 hydrochlorid (1365986-44-2(free
Protein kinase inhibitors 1 is a novel inhibitor of HIPK2 with an IC50 of 74 nM and Kd of 9.5 nM.
价 格：￥电议型 号：T4692产 地：中国大陆
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T3190PIK-inhibitorsMDK34597
PIK-inhibitors is a pan PI3K inhibitors, an analog of PI-103.
价 格：￥电议型 号：T3190产 地：中国大陆
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T4636Protein kinase inhibitors 1Protein kinase inhibitors 1
Protein kinase inhibitors 1 is a novel inhibitor of HIPK2 with an IC50 of 74 nM and Kd of 9.5 nM.
价 格：￥电议型 号：T4636产 地：美洲
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T81115sPLA2-IIA Inhibitor；化合物 sPLA2-IIA InhibitorsPLA2-IIA Inhibitor
The sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK, specifically cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2), which interacts with human IIA phospholipase A2 (hGIIA) to impede its ester bond hydrolyzing function. As part of the esterase superfamily, sPLA2 enzymatically cleaves the sn-2 ester bond in glycerophospholipids, releasing arachidonic acid and lysophospholipids[1].
价 格：￥电议型 号：T81115产 地：中国大陆
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T7263SMS2-IN-2；化合物SMS2-IN-2SMS2 inhibitors；SMS2 inhibitors
SMS2-IN-2 (SMS2 inhibitors) is a potent, selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, (IC50s of 100 and 56 μM for SMS2 and SMS1, respectively). SMS2-IN-2 has anti-chronic inflammatory activity.
价 格：￥电议型 号：T7263产 地：中国大陆
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T71947SGK1 inhibitor；化合物 SGK1 inhibitorSGK1 inhibitor
SGK1 inhibitor is an inhibitor of serum- and glucocorticoid-regulated kinase 1 (SGK1) and SGK2. It is selective for SGK1 and SGK2 over SGK3 in the presence of a high concentration of ATP. SGK1 inhibitor prevents phosphorylation of GSK3β in U2OS cells and decreases cell viability in BYL719-insensitive HCC1954 cells when used in combination with the PI3Kα inhibitor BYL719. SGK1 inhibitor reduces tumor growth in an HCC1954 mouse xenograft model when administered in combination with BYL719.
价 格：￥电议型 号：T71947产 地：中国大陆
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T71175SCD1 Inhibitor；化合物 SCD1 InhibitorSCD1 Inhibitor
SCD1 Inhibitor is a novel stearoyl-CoA desaturase1 (SCD1) inhibitor.
价 格：￥电议型 号：T71175产 地：中国大陆
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T4692Protein kinase inhibitors 1 hydrochlorid；化合物T4692Protein kinase inhibitors 1 hydrochlorid (1365986-4
Protein kinase inhibitors 1 hydrochlorid (Protein kinase inhibitors 1 hydrochlorid (1365986-44-2(free base))) is a novel inhibitor of HIPK2 with an IC50 of 74 nM and Kd of 9.5 nM.
价 格：￥电议型 号：T4692产 地：中国大陆
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T4636Protein kinase inhibitors 1；化合物Protein kinase inhibitors 1Protein kinase inhibitors 1
Protein kinase inhibitors 1 is a novel inhibitor of HIPK2 with an IC50 of 74 nM and Kd of 9.5 nM.
价 格：￥电议型 号：T4636产 地：中国大陆
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T4216STAT5-IN-1；化合物STAT5 InhibitorSTAT5 Inhibitor；STAT5 Inhibitor
STAT5-IN-1 (STAT5 Inhibitor) is a cell-permeable inhibitor which suppresses Stat5 via binding to the SH2 domain.
价 格：￥电议型 号：T4216产 地：中国大陆
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T39860Protein kinase inhibitors 1 hydrochloride；Protein kinase inhibitors 1 hydrochlorideProtein kinase in
Protein Kinase Inhibitors 1 Hydrochloride effectively inhibits HIPK2, demonstrating high potency with IC50 values of 136 nM for HIPK1 and 74 nM for HIPK2, alongside a dissociation constant (Kd) of 9.5 nM for HIPK2.
价 格：￥电议型 号：T39860产 地：中国大陆
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T3190PIK-inhibitors；化合物PIK-inhibitorsMDK34597；MDK34597
PIK-inhibitors (MDK34597) is a pan PI3K inhibitors, an analog of PI-103.
价 格：￥电议型 号：T3190产 地：中国大陆
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T23420Tankyrase Inhibitors (TNKS) 22；化合物 T23420Tankyrase Inhibitors (TNKS) 22
Tankyrase Inhibitors 22 is a potent, selective, and orally bioavailable inhibitor of tankyrase (IC50: 0.1nM).
价 格：￥电议型 号：T23420产 地：中国大陆
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T23419Tankyrase Inhibitors (TNKS) 49；化合物 T23419Tankyrase Inhibitors (TNKS) 49
Tankyrase Inhibitors 49 is an effective, selective, and orally bioavailable inhibitor of tankyrase (IC50: 0.1nM).
价 格：￥电议型 号：T23419产 地：中国大陆
