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Search Results for " mek in 1 "

21

抑制剂 & 化合物

1

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T10675	MEK-IN-1	MEK	MAPK
	MEK-IN-1 is a MEK inhibitor.
T28012	MEK-IN-4	MEK	MAPK
	MEK-IN-4 是一种 MEK 抑制剂，可用于研究炎症性疾病和癌症。
T74360	MEK/PI3K-IN-1
	MEK/PI3K-IN-1（compound 6r）是一种高效的MEK/PI3K抑制剂，IC50值为124 nM（MEK1）、130 nM（PI3Kα）及236 nM（PI3Kδ）。该化合物能够降低pAKT和pERK1/2的活性，并展现对肿瘤细胞的抗增殖作用。
T40206	MEK4 inhibitor-1 MEK4 inhibitor-1
	MEK4 inhibitor-1 is a newly developed compound specifically designed to inhibit the activity of MEK4, a key enzyme involved in pancreatic adenocarcinoma, with an IC 50 value of 61 nM.
T76556	MEK1 Derived Peptide Inhibitor 1
	MEK1Derived Peptide Inhibitor 1，一种肽抑制剂，以IC50值30 μM抑制MEK1激活ERK2。适用于细胞渗透性研究。
T76557	Myristoyl-MEK1 Derived Peptide Inhibitor 1
	Myristoyl-MEK1 Derived Peptide Inhibitor 1 是MEK1Derived Peptide Inhibitor 1 的豆蔻酰化形式。Myristoyl-MEK1 Derived Peptide Inhibitor 1 抑制ERK 的激活，IC50为 10 μM。
T80543	STE-MEK1(13) ERK Activation Inhibitor Peptide,Ste-MPKKKPTPIQLNP-NH₂	ERK	MAPK
	STE-MEK1(13)（Ste-MPKKKPTPIQLNP-NH2）为一细胞渗透性ERK1/2抑制剂，IC50值为13-30μM，可抑制ERK1/2磷酸化。
T79144	PROTAC MEK1 Degrader-1	PROTACs	PROTAC
	PROTACMEK1Degrader-1是一种针对MEK1的PROTAC，显示出pIC50值为7.0。该化合物由MEK1抑制剂与von Hippel-Lindau配体构成，能够抑制ERK1/2的磷酸化，并对A375细胞展现出抗增殖活性。
T72407	c-Met/MEK1/Flt-3-IN-1
	Antiproliferative against-3 具有良好的抗癌细胞增殖活性，对 Hela、A549 和 MCF-7 的细胞的 IC50值分别为 0.21 µM、0.39 µM 和 0.33 µM。Antiproliferative against-3 (comp 33) 剂量依赖性的诱导 A549 细胞的凋亡，并将细胞阻滞在 G1 期。
T63547	MEK1/2-IN-2
	MEK1/2-IN-2 是有效的、ATP 竞争性的 MEK1/2 抑制剂，对野生型 MEK1/2 和一组 MEK1/2 突变细胞表现出同等的抑制效果。
T21635	PD184161	MEK	MAPK
	PD 184161 是一种口服有效的，时间和浓度依赖的 MEK 抑制剂，IC50为10-100 nM。它诱导抑郁样行为，抑制细胞增殖并诱导细胞凋亡。
T0468	Lidocaine Lignocaine,Alphacaine,Xylocaine,利多卡因	Apoptosis; ERK; NF-κB; MEK; Sodium Channel; Histamine Receptor	Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Neuroscience; NF-κB
	Lidocaine (Alphacaine) 是一种酰胺衍生物，抑制涉及复杂电压和依赖性的钠通道，可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长，迁移和侵袭。
T75110	Trametiglue
	Trametiglue 是 Trametinib 的衍生物，通过独特的界面结合相互作用，以前所未有的效力和选择性靶向 KSR-MEK 和 RAF-MEK。
T74361	MEK/PI3K-IN-2
	MEK/PI3K-IN-2 (compound 6s) 是一种有效的 MEK/PI3K 抑制剂，其 IC50值分别为 352 nM (MEK1), 107 nM (PI3Kα), 和 137 nM (PI3Kδ)。MEK/PI3K-IN-2 抑制 pAKT 和 pERK1/2 水平。MEK/PI3K-IN-2 对肿瘤细胞具有抗增殖活性。
T79048	MEK-IN-6 hydrate	MEK	MAPK
	MEK-IN-6 hydrate（compound 69）为MEK抑制剂，其对A375细胞展现出强效性，IC50仅为2 nM。
T79047	MEK-IN-6	ERK	MAPK
	MEK-IN-6（Example 69）是一种针对MEK的抑制剂，在A375细胞中有效抑制ERK1/2（THR202/Tyr204）的磷酸化，其IC50值为2 nM。此化合物主要应用于癌症研究领域。
T61627	iMDK quarterhydrate
	iMDK quarterhydrate, a potent PI3K inhibitor, is effective in inhibiting the growth factor MDK (also known as midkine or MK) while demonstrating suppression of non-small cell lung cancer (NSCLC). In combination with a MEK inhibitor, iMDK quarterhydrate demonstrates cooperative inhibition of NSCLC without causing harm to normal cells and mice [1].
T78608	Anticancer agent 164	Apoptosis	Apoptosis
	CML-IN-1（compound 7）是一种高效抗癌药物，针对人类慢性粒细胞白血病（CML）细胞系K562，能有效诱导凋亡（apoptosis）。该化合物主要通过显著抑制PI3K/Akt信号通路的蛋白磷酸化来发挥作用，同时CML-IN-1（compound 4）也能通过抑制结直肠癌的MEK/ERK信号通路来阻止细胞增殖。
T35594	Cuspin-1
	The Survival of Motor Neurons (SMN) protein participates in RNA splicing. Decreases in SMN, typically a consequence of defects in the smn1 gene, result in the death of motor neurons and lead to the neurodegenerative disease, spinal muscular atrophy (SMA). Cuspin-1 is a small molecule upregulator of SMN that has been shown in vitro to increase levels of SMN in SMA patient fibroblasts by 50% at 18 μM. Its mechanism of action is thought to involve increased phosphorylation of ERK to initiate Ras-Ra...
TP2091	Antisauvagine-30
	Potent, selective and competitive corticotropin-releasing factor CRF2 receptor antagonist (Kd values are 1.4 and 153.6 nM for binding to mouse CRF2β and rat CRF1 receptors respectively). Inhibits sauvagine-stimulated cAMP accumulation in HEK-mCRF2β cells
T35536	Tpl2 Kinase Inhibitor (hydrochloride)
	Tpl2 kinase inhibitor is an inhibitor of tumor progression locus 2 (Tpl2; IC50= 0.05 μM).1It is selective for Tpl2 over MEK, p38 MAPK, Src, MK2, and PKC (IC50s = >40, 180, >400, 110, and >400 μM, respectively). Tpl2 kinase inhibitor inhibits LPS-induced TNF-α production in isolated human monocytes and whole blood (IC50s = 0.7 and 8.5 μM, respectively). It enhances differentiation induced by calcitriol in HL-60 and U937 leukemia cells when used at a concentration of 5 μM.2Tpl2 kinase inhibitor (5...

化合物

Cat.No: T10675

Target: MEK

Cat.No: T28012

Target: MEK

MEK/PI3K-IN-1

Cat.No: T74360

MEK4 inhibitor-1

Cat.No: T40206

Synonym: MEK4 inhibitor-1

MEK1 Derived Peptide Inhibitor 1

Cat.No: T76556

Myristoyl-MEK1 Derived Peptide Inhibitor 1

Cat.No: T76557

Cat.No: T80543

Synonym: ERK Activation Inhibitor Peptide,Ste-MPKKKPTPIQLNP-NH₂

Target: ERK

PROTAC MEK1 Degrader-1

Cat.No: T79144

Target: PROTACs

c-Met/MEK1/Flt-3-IN-1

Cat.No: T72407

Cat.No: T63547

Cat.No: T21635

Target: MEK

Cat.No: T0468

Synonym: Lignocaine,Alphacaine,Xylocaine,利多卡因

Target: Apoptosis, ERK, NF-κB, MEK, Sodium Channel, Histamine Receptor

Cat.No: T75110

MEK/PI3K-IN-2

Cat.No: T74361

MEK-IN-6 hydrate

Cat.No: T79048

Target: MEK

Cat.No: T79047

Target: ERK

iMDK quarterhydrate

Cat.No: T61627

Anticancer agent 164

Cat.No: T78608

Target: Apoptosis

Cat.No: T35594

Antisauvagine-30

Cat.No: TP2091

Tpl2 Kinase Inhibitor (hydrochloride)

Cat.No: T35536

Cat. No.	Product Name	Target	Signaling Pathways
T6S1740	Nardosinone 苷松新酮,甘松新酮	Others	Others
	Nardosinone 是一个 dbcAMP 和 staurosporine 的神经生成作用增强剂，分离自Nardostachys chinensis 中。Nardosinone 可能成为一种有用的药理学工具，不仅可用于研究神经生长因子 (NGF) 的作用机理，而且可用于研究神经毒性物质的作用机理。

天然产物

Cat.No: T6S1740

Synonym: 苷松新酮,甘松新酮

Target: Others

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