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Glucokinase

Glucokinase

Glucokinase is an enzyme that facilitates phosphorylation of glucose to glucose-6-phosphate. Glucokinase occurs in cells in the liver and pancreas of humans and most other vertebrates. In each of these organs it plays an important role in the regulation of carbohydrate metabolism by acting as a glucose sensor, triggering shifts in metabolism or cell function in response to rising or falling levels of glucose, such as occur after a meal or when fasting. Mutations of the gene for this enzyme can cause unusual forms of diabetes or hypoglycemia.Glucokinase (GK) is a hexokinase isozyme, related homologously to at least three other hexokinases. All of the hexokinases can mediate phosphorylation of glucose to glucose-6-phosphate (G6P), which is the first step of both glycogen synthesis and glycolysis.
TargetMol
1 2
Cat. No. Product Name CAS No. Purity Chemical Structure
TN5192 Tuberosin
化合物 TN5192
41347-45-9 98%
TargetMol Chemical Structure Tuberosin
Tuberosin shows anti-inflammatory and antioxidant activities.It demonstrated a significantly potent inhibition on yeast α-glucosidase in a dose dependent manner....
TN5090 Tachioside
化合物 TN5090
109194-60-7 98%
TargetMol Chemical Structure Tachioside
Tachioside has antiobesity, antioxidant and α-glucosidase inhibitory activities, it decreases lipid content in 3T3-L1 adipocytes by inhibiting lipogenesis, shows...
TN4793 Pinoresinol diacetate
化合物 TN4793
32971-25-8 98%
TargetMol Chemical Structure Pinoresinol diacetate
Pinoresinol diacetate inhibits the enzyme α-glucosidase in vitro and may therefore act as a hypoglycemic agent.
T10751 Cefetrizole
头孢三唑
65307-12-2 98%
TargetMol Chemical Structure Cefetrizole
Ceftezole is an α-Glucosidase inhibitor (IC50: 2.1 μM; Ki: 0.578 μM).
TN5094 Tangshenoside I
党参苷 I
117278-74-7 98%
TargetMol Chemical Structure Tangshenoside I
Tangshenoside I might be a potential bioactive marker related to the hematopoietic and immunologic functions of Codonopsis Radix, which could be recommended as t...
TN3745 Cyclomusalenone
化合物 TN3745
30452-60-9 98%
TargetMol Chemical Structure Cyclomusalenone
Cyclomusalenone is a potent α-glucosidase inhibitor.
T11749 KDM4-IN-2
化合物 T11749
2369607-62-3 98%
TargetMol Chemical Structure KDM4-IN-2
KDM4-IN-2 is a potent and selective KDM4/KDM5 dual inhibitor with Kis of 4 and 7 nM for KDM4A and KDM5B, respectively.
TN4174 Guajadial
化合物 TN4174
959860-49-2 98%
TargetMol Chemical Structure Guajadial
Guajadial shows α-glucosidase inhibitory activities significantly and its activity was better than that of Acarbose.Guajadial may act as Selective Estrogen Recep...
T16480 PF-04991532
化合物 T16480
1215197-37-7 98%
TargetMol Chemical Structure PF-04991532
PF-04991532 is an effective, hepatoselective glucokinase activator. It has EC50s of 80 and 100 nM in human and rat, respectively.
T6759 AP-III-a4
化合物AP-III-a4
1177827-73-4 99.90%
TargetMol Chemical Structure AP-III-a4
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
化合物POMHEX
2004714-34-3 99.88%
TargetMol Chemical Structure POMHEX
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。
T11741 KAN0438757
化合物KAN0438757
1451255-59-6 99.8%
TargetMol Chemical Structure KAN0438757
KAN0438757 是一种选择性强效的代谢激酶 PFKFB3 抑制剂,IC50值为 0.19 μM。
T64320 ML251
化合物ML251 
1486482-16-9 99.79%
TargetMol Chemical Structure ML251
ML251 是一种有效的新型纳摩尔 T. brucei 和 T. cruzi 磷酸果糖激酶抑制剂,对 T. brucei PFK 和 T. cruzi PFK 的 IC50值为 0.37和 0.13 μM,可研究寄生虫。
T15159 Dorzagliatin
化合物Dorzagliatin
1191995-00-2 99.74%
TargetMol Chemical Structure Dorzagliatin
Dorzagliatin (HMS5552) 是双重作用的葡萄糖激酶 (glucokinase;GK) 激活剂,可改善 2 型糖尿病的血糖控制,提高胰腺 β 细胞功能。
T22223 3PO
化合物3PO
18550-98-6 99.67%
TargetMol Chemical Structure 3PO
3PO 是一种 PFKFB3 的小分子抑制剂,IC50值为22.9 μM。它抑制几种人类恶性造血和腺癌细胞系的增殖,IC50在1.4到24 μM 之间。它抑制葡萄糖摄取,并降低 Fru-2,6-BP、乳酸、ATP、NAD+ 和 NADH 的细胞内浓度。
T3312 AM-2394
化合物AM2394
1442684-77-6 99.58%
TargetMol Chemical Structure AM-2394
AM-2394 是新型的 glucokinase 激活剂 (GKA)。它能够激活葡萄糖激酶 (GK),EC50=60 nM。
T3386 Kaempferitrin
山奈苷
482-38-2 99.51%
TargetMol Chemical Structure Kaempferitrin
Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物,具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用,可激活胰岛素信号传导。
T26712 AZD-1656
化合物AZD-1656
919783-22-5 99.37%
TargetMol Chemical Structure AZD-1656
AZD-1656 是口服有效的葡萄糖激酶选择性激活剂,EC50为 60 nM。AZD1656在2 型糖尿病中有研究的价值。
T19500 Palmitelaidic Acid
软脂酸
10030-73-6 99.36%
TargetMol Chemical Structure Palmitelaidic Acid
trans-Palmitelaidic Acid (trans-Palmitoleic acid) 是palmitoleic acid 的反式异构体。Palmitoleic acid 是血清和组织中最丰富的脂肪酸之一。
T4049 Genz-123346 free base
化合物Genz-123346 free base
491833-30-8 99.23%
TargetMol Chemical Structure Genz-123346 free base
Genz-123346 free base 是一种能够阻断神经酰胺向GL1转化的GL1合酶的抑制剂,其抑制GM1的IC50值为14 nM。
Tuberosin
TN5192
Tuberosin shows anti-inflammatory and antioxidant activities.It demonstrated a significantly potent inhibition on yeast α-glucosidase in a dose dependent manner....
Tachioside
TN5090
Tachioside has antiobesity, antioxidant and α-glucosidase inhibitory activities, it decreases lipid content in 3T3-L1 adipocytes by inhibiting lipogenesis, shows...
Pinoresinol diacetate
TN4793
Pinoresinol diacetate inhibits the enzyme α-glucosidase in vitro and may therefore act as a hypoglycemic agent.
Cefetrizole
T10751
Ceftezole is an α-Glucosidase inhibitor (IC50: 2.1 μM; Ki: 0.578 μM).
Tangshenoside I
TN5094
Tangshenoside I might be a potential bioactive marker related to the hematopoietic and immunologic functions of Codonopsis Radix, which could be recommended as t...
Cyclomusalenone
TN3745
Cyclomusalenone is a potent α-glucosidase inhibitor.
KDM4-IN-2
T11749
KDM4-IN-2 is a potent and selective KDM4/KDM5 dual inhibitor with Kis of 4 and 7 nM for KDM4A and KDM5B, respectively.
Guajadial
TN4174
Guajadial shows α-glucosidase inhibitory activities significantly and its activity was better than that of Acarbose.Guajadial may act as Selective Estrogen Recep...
PF-04991532
T16480
PF-04991532 is an effective, hepatoselective glucokinase activator. It has EC50s of 80 and 100 nM in human and rat, respectively.
AP-III-a4
T6759
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。
POMHEX
T36491
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。
KAN0438757
T11741
KAN0438757 是一种选择性强效的代谢激酶 PFKFB3 抑制剂,IC50值为 0.19 μM。
ML251
T64320
ML251 是一种有效的新型纳摩尔 T. brucei 和 T. cruzi 磷酸果糖激酶抑制剂,对 T. brucei PFK 和 T. cruzi PFK 的 IC50值为 0.37和 0.13 μM,可研究寄生虫。
Dorzagliatin
T15159
Dorzagliatin (HMS5552) 是双重作用的葡萄糖激酶 (glucokinase;GK) 激活剂,可改善 2 型糖尿病的血糖控制,提高胰腺 β 细胞功能。
3PO
T22223
3PO 是一种 PFKFB3 的小分子抑制剂,IC50值为22.9 μM。它抑制几种人类恶性造血和腺癌细胞系的增殖,IC50在1.4到24 μM 之间。它抑制葡萄糖摄取,并降低 Fru-2,6-BP、乳酸、ATP、NAD+ 和 NADH 的细胞内浓度。
AM-2394
T3312
AM-2394 是新型的 glucokinase 激活剂 (GKA)。它能够激活葡萄糖激酶 (GK),EC50=60 nM。
Kaempferitrin
T3386
Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物,具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用,可激活胰岛素信号传导。
AZD-1656
T26712
AZD-1656 是口服有效的葡萄糖激酶选择性激活剂,EC50为 60 nM。AZD1656在2 型糖尿病中有研究的价值。
Palmitelaidic Acid
T19500
trans-Palmitelaidic Acid (trans-Palmitoleic acid) 是palmitoleic acid 的反式异构体。Palmitoleic acid 是血清和组织中最丰富的脂肪酸之一。
Genz-123346 free base
T4049
Genz-123346 free base 是一种能够阻断神经酰胺向GL1转化的GL1合酶的抑制剂,其抑制GM1的IC50值为14 nM。
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