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Search Results for " enolase "

10

抑制剂 & 化合物

3

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T6759	AP-III-a4 ENOblock	Glucokinase	Metabolism
	AP-III-a4 (ENOblock) 是第一个非底物类似物，可直接与烯醇酶结合，IC50=0.576 uM，可阻碍体内癌细胞转移。
T36491	POMHEX	Glucokinase	Metabolism
	Pomhex 是一种具有抗癌活性的细胞渗透性强效烯醇化酶抑制剂，可用于癌症致死率的研究。Pomhex是一种外消旋混合物，是一种强效且具有选择性的ENO2抑制剂。
T23446	TCS 2210	Others	Others
	TCS 2210是间充质干细胞中神经元分化的诱导剂，并增加神经元标志物β-III 管蛋白的表达和神经元特异性烯醇酶的表达。
T37185	D-(-)-3-Phosphoglyceric acid disodium 3-Phospho-D-glyceric acid disodium	Others	Others
	D-(-)-3-Phosphoglyceric acid disodium (3-Phospho-D-glyceric acid disodium) 是糖酵解、糖原合成以及丝氨酸、甘氨酸、苏氨酸生物合成等过程中的重要中间体,竞争性抑制酵母烯醇化酶 (enolase)。作为中间体它还在植物、真核细胞以及原核细胞许多的生物合成信号通路中发挥许多作用。
T39419	Hex
	Hex is a potent inhibitor of enolase, exhibiting inhibitory activity with Ki values of 74.4 nM and 269.4 nM against ENO2 and ENO1, respectively.
T70903	KRH102053
	KRH102053 is a HIF-1alpha inhibitor. KRH102053 decreased the protein level of HIF-1alpha and the mRNA levels of HIF-regulated downstream target genes, such as vascular endothelial growth factor, aldolase A, enolase 1 and monocarboxylate transporter 4. Consistent with these results, KRH102053 also inhibited the rates of HIF-related migration and invasion of HOS cells as well as the degree of tube formation in human umbilical vein endothelium cells.
T80931	Tri-valine NSC 35938
	Tri-valine (NSC 35938) 为多肽类化合物，可从肌酸激酶 (Creatine kinase)、β-烯醇化酶、三磷酸异构酶 (Triosephosphate isomerase) 及甘油醛 3-磷酸脱氢酶中分离得到。
T6759L	AP-III-a4 hydrochloride (1177827-73-4 free base) ENOblock hydrochloride,AP-III-a4 hydrochloride	Others	Others
	AP-III-a4 hydrochloride (ENOblock hydrochloride) is a novel small molecule which is the first, nonsubstrate analogue that directly binds to enolase and inhibits its activity (IC50=0.576 uM); inhibit cancer cell metastasis in vivo. IC50 value: 0.576 uM [1]
T78124	SF2312 ammonium	Antibiotic	Microbiology/Virology
	SF2312铵是SF2312的铵盐形式，后者为一种膦酸盐类抗生素兼烯醇酶抑制剂。该化合物可从放线菌小单孢菌分离而得，在缺氧环境中活性显著。SF2312对ENO1基因缺失的神经胶质瘤细胞显示出选择性毒杀作用。
T68511	KRH102140
	KRH102140 is a potent activator of PHD2. KRH102140, which has a structure similar to KRH102053. KRH102140 more efficiently suppressed HIF-1α than KRH102053 in human osteosarcoma cells under hypoxia. Furthermore, KRH102140 decreased the mRNA levels of HIF-regulated downstream target genes associated with angiogenesis and energy metabolism such as vascular endothelial growth factor, adrenomedullin, Glut1, aldolase A, enolase 1 and monocarboxylate transporter 4. KRH102140 also inhibited tube format...

化合物

Cat.No: T6759

Synonym: ENOblock

Target: Glucokinase

Cat.No: T36491

Target: Glucokinase

Cat.No: T23446

Target: Others

D-(-)-3-Phosphoglyceric acid disodium

Cat.No: T37185

Synonym: 3-Phospho-D-glyceric acid disodium

Target: Others

Cat.No: T39419

Cat.No: T70903

Cat.No: T80931

Synonym: NSC 35938

AP-III-a4 hydrochloride (1177827-73-4 free base)

Cat.No: T6759L

Synonym: ENOblock hydrochloride,AP-III-a4 hydrochloride

Target: Others

SF2312 ammonium

Cat.No: T78124

Target: Antibiotic

Cat.No: T68511

Cat. No.	Product Name	Target	Signaling Pathways
T4929	L-2-Phosphoglyceric acid L-GLYCERATE 3-PHOSPHATE 二钠盐,L-2-Phosphoglyceric acid disodium salt h	Others; Endogenous Metabolite	Metabolism; Others
	L-2-Phosphoglyceric acid (L-2-Phosphoglyceric acid disodium salt) 是内源性代谢产物的一种。
T28764	SF2312 SF-2312,SF 2312
	SF2312 is an enolase inhibitor produced by the actinomycete Micromonospora, which is active under anaerobic conditions.
T5141	L-2-Phosphoglyceric acid disodium salt hydrate L-2-Phosphoglyceric acid 二钠盐水合物	Others	Others
	L-2-Phosphoglyceric acid disodium salt hydrate 是一种甘油酸，可作为糖酵解第九步的底物。它被烯醇化酶催化为磷酸烯醇式丙酮酸 (PEP)，这是葡萄糖转化为丙酮酸的倒数第二个步骤。

天然产物

L-2-Phosphoglyceric acid

Cat.No: T4929

Synonym: L-GLYCERATE 3-PHOSPHATE 二钠盐,L-2-Phosphoglyceric acid disodium salt h

Target: Others, Endogenous Metabolite

Cat.No: T28764

Synonym: SF-2312,SF 2312

L-2-Phosphoglyceric acid disodium salt hydrate

Cat.No: T5141

Synonym: L-2-Phosphoglyceric acid 二钠盐水合物

Target: Others

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