Glucokinase
Glucokinase phosphorylates glucose to produce glucose-6-phosphate during the initial step of glycogenesis. Pancreatic glucokinase regulates insulin secretion. Hepatic glucokinase facilitates the uptake and conversion of glucose.
Products Related to Glucokinase(17)
- GC31514PF-04991532CAS: 1215197-37-7Purity: >98%
PF-04991532 is a potent, hepatoselective glucokinase activator with EC50s of 80 and 100 nM in human and rat, respectively.
- GC33765Palmitelaidic Acid (9-trans-Hexadecenoic acid)CAS: 10030-73-6Purity: >98.00%
Palmitelaidic Acid (9-trans-Hexadecenoic acid) is a trans isomer of palmitoleic acid and dietary fatty acid that has been found in dairy fat products and various partially hydrogenated oils.
- GC36881PF-04937319CAS: 1245603-92-2Purity: >99.50%
PF-04937319 is a glucokinase activator (GKA) with EC50 value of 154.4 ?μM, one of the most promising strategies for the treatment of type 2 diabetes mellitus.
- GC37546Ro 28-1675CAS: 300353-13-3Purity: >99.50%
Ro 28-1675 is a potent allosteric glucokinase (GK) activator with an EC50 of 54 nM.
- GC61749GKA50 quarterhydratePurity: >98%
GKA50 quarterhydrate is a potent glucokinase activator (EC50=33 nM at 5 mM glucose) and stimulates insulin release from mouse islets of Langerhans.
- GC66015IHVR-11029CAS: 1383152-30-4Purity: >99.00%
IHVR-11029 is a small molecule inhibitor of ER α-glucosidases, with an EC50 of 0.09 μM.
- GC68783BMS-820132CAS: 1001419-18-6Purity: >99.00%
BMS-820132 is an orally effective, partial glucokinase activator with an AC50 of 29 nM. It can lower glucose levels in normal rat oral glucose tolerance test (OGTT) models but does not reduce glucose levels in Zucker diabetic fatty (ZDF) rats. BMS-820132 has pharmacological toxicity secondary to potent GK activation.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC13124 | LY2608204 | 1234703-40-2 | >98.00% | |
LY2608204 (LY2608204) is a activator of glucokinase (GK) with EC50 of 42 nM. | ||||
| GC18214 | AM2394 | 1442684-77-6 | >99.00% | |
A glucokinase activator | ||||
| GC19029 | AMG-3969 | 1361224-53-4 | >99.50% | |
AMG-3969 is a potent glucokinase-glucokinase regulatory protein interaction (GK-GKRP) disruptor with an IC50 of 4 nM. | ||||
| GC31514 | PF-04991532 | 1215197-37-7 | >98% | |
PF-04991532 is a potent, hepatoselective glucokinase activator with EC50s of 80 and 100 nM in human and rat, respectively. | ||||
| GC31618 | PSN-GK1 | 745051-61-0 | >98% | |
PSN-GK1 is a potent glucokinase activator with an EC50 of 0.13 μM. | ||||
| GC33765 | Palmitelaidic Acid (9-trans-Hexadecenoic acid) | 10030-73-6 | >98.00% | |
Palmitelaidic Acid (9-trans-Hexadecenoic acid) is a trans isomer of palmitoleic acid and dietary fatty acid that has been found in dairy fat products and various partially hydrogenated oils. | ||||
| GC36881 | PF-04937319 | 1245603-92-2 | >99.50% | |
PF-04937319 is a glucokinase activator (GKA) with EC50 value of 154.4 ?μM, one of the most promising strategies for the treatment of type 2 diabetes mellitus. | ||||
| GC37546 | Ro 28-1675 | 300353-13-3 | >99.50% | |
Ro 28-1675 is a potent allosteric glucokinase (GK) activator with an EC50 of 54 nM. | ||||
| GC38784 | GKA50 | 851884-87-2 | >98% | |
GKA50 is a potent glucokinase activator (EC50=33 nM at 5 mM glucose). | ||||
| GC44210 | MK-0941 | 1137916-97-2 | >98.50% | |
MK-0941 is a glucokinase activator with EC50 values of 0.24 and 0.065 μM at low (2.5 mM) and high (10 mM) concentrations of glucose, respectively. | ||||
| GC61749 | GKA50 quarterhydrate | - | >98% | |
GKA50 quarterhydrate is a potent glucokinase activator (EC50=33 nM at 5 mM glucose) and stimulates insulin release from mouse islets of Langerhans. | ||||
| GC62846 | AR453588 | 1065609-00-8 | >99.50% | |
AR453588 is a potent and orally bioavailable anti-diabetic glucokinase activator, with an EC50 of 42 nM. | ||||
| GC66015 | IHVR-11029 | 1383152-30-4 | >99.00% | |
IHVR-11029 is a small molecule inhibitor of ER α-glucosidases, with an EC50 of 0.09 μM. | ||||
| GC67901 | Glucokinase activator 3 | 1001417-92-0 | >98% | |
| GC68003 | Cadisegliatin | 859525-02-3 | >98% | |
| GC68783 | BMS-820132 | 1001419-18-6 | >99.00% | |
BMS-820132 is an orally effective, partial glucokinase activator with an AC50 of 29 nM. It can lower glucose levels in normal rat oral glucose tolerance test (OGTT) models but does not reduce glucose levels in Zucker diabetic fatty (ZDF) rats. BMS-820132 has pharmacological toxicity secondary to potent GK activation. | ||||
| GC70590 | AMG-1694 | 1361217-07-3 | - | |
AMG-1694 is a potent glucokinase–glucokinase regulatory protein (GK-GKRP) disruptors and promotes the dissociation of the GK-GKRP complex with an IC50 of 7 nM, indirectly increasing GK enzymatic activity. | ||||
