Mitophagy
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Mitophagy is the selective degradation of mitochondria by autophagy.
Mitochondria are essential organelles that regulate cellular energy homeostasis and cell death. The removal of damaged mitochondria through autophagy, a process called mitophagy, is thus critical for maintaining proper cellular functions. Indeed, mitophagy has been recently proposed to play critical roles in terminal differentiation of red blood cells, paternal mitochondrial degradation, neurodegenerative diseases, and ischemia or drug-induced tissue injury.
Autophagy and mitophagy are important cellular processes that are responsible for breaking down cellular contents, preserving energy and safeguarding against accumulation of damaged and aggregated biomolecules.
Products Related to Mitophagy(84)
- GC10480Betulinic acidCAS: 472-15-1Purity: >98.00%
Betulinic acid is a natural pentacyclic triterpenoid compound and an inhibitor of eukaryotic topoisomerase I with an IC 50 value of 5 μM.
- GC10585Simvastatin (Zocor)CAS: 79902-63-9Purity: >98.00%
Simvastatin (Zocor) (MK 733) is a competitive inhibitor of HMG-CoA reductase with a Ki of 0.2 nM.
- GC107103-MethyladenineCAS: 5142-23-4Purity: >98.00%
3-Methyladenine is a PI3K inhibitor with IC 50 values of 25μM and 60μM for Vps34 and PtdIns3Kγ, respectively.
- GC11332PitavastatinCAS: 147511-69-1Purity: >98.00%
Pitavastatin is a 3-Hydroxymethyl-3-glutaryl-CoA (HMG-CoA) reductase inhibitors. The IC 50 value of the HMG-CoA reductase activity in the Hep G2 cells for Pitavastatin was 5.8nM.
- GC1172017-AAG (KOS953)CAS: 75747-14-7Purity: >98.00%
17-AAG (KOS953) is a potent Hsp90 inhibitor (IC 50 =5nM).
- GC12339IvermectinCAS: 70288-86-7Purity: >98.00%
Ivermectin is a macrolide endectocide with activity against both endoparasites and ectoparasites.
- GC12807U0126-EtOHCAS: 1173097-76-1Purity: >98.00%
U0126-EtOH is a non-ATP competitive and selective inhibitor of MEK1 and MEK2 with IC 50 values of 72nM and 58nM, respectively.
- GC13001SB 203580 hydrochlorideCAS: 869185-85-3Purity: >98.00%
Adezmapimod (SB 203580) hydrochloride is a selective and ATP-competitive p38 MAPK inhibitor with IC50s of 50 nM and 500 nM for SAPK2a/p38 and SAPK2b/p38β2, respectively.
- GC13554Deferoxamine mesylateCAS: 138-14-7Purity: >98.00%
Deferoxamine mesylate is an iron chelator that binds Fe(III) and many other metal cations.
- GC14191Ruxolitinib (INCB18424)CAS: 941678-49-5Purity: >98.00%
Ruxolitinib (INCB018424), as an inhibitor, inhibits Janus-associated kinases (JAKs)JAK1 and JAK2 with IC 50 values of 3.3 nM and 2.8 nM, respectively.
- GC14553ResveratrolCAS: 501-36-0Purity: >99.50%
Resveratrol (trans-Resveratrol; SRT501) is a phytoalexin.
- GC14591Hemin chlorideCAS: 16009-13-5Purity: >98.00%
Hemin chloride, a substrate of heme oxygenase (HO)-1, induces HO-1 expression on a variety of cells to exert anti-oxidant and anti-inflammatory roles.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GA10942 | H-D-Gln-OH | 5959-95-5 | >99.00% | |
| GC10200 | Mdivi 1 | 338967-87-6 | >98.00% | |
Mdivi-1 (Mitochondrial division inhibitor 1) inhibits traumatic brain injury (TBI)-induced dynamin-related protein 1(Drp1) up-regulation, autophagy dysfunction and mitophagy activation. | ||||
| GC10480 | Betulinic acid | 472-15-1 | >98.00% | |
Betulinic acid is a natural pentacyclic triterpenoid compound and an inhibitor of eukaryotic topoisomerase I with an IC 50 value of 5 μM. | ||||
| GC10518 | AICAR | 2627-69-2 | >99.00% | |
AICAR (also called acadesine) is a purine nucleoside. | ||||
| GC10580 | AICAR phosphate | 681006-28-0 | >98.00% | |
AMPK activator | ||||
| GC10585 | Simvastatin (Zocor) | 79902-63-9 | >98.00% | |
Simvastatin (Zocor) (MK 733) is a competitive inhibitor of HMG-CoA reductase with a Ki of 0.2 nM. | ||||
| GC10710 | 3-Methyladenine | 5142-23-4 | >98.00% | |
3-Methyladenine is a PI3K inhibitor with IC 50 values of 25μM and 60μM for Vps34 and PtdIns3Kγ, respectively. | ||||
| GC11237 | Dexamethasone acetate | 1177-87-3 | >98.00% | |
IL Receptor modulator | ||||
| GC11332 | Pitavastatin | 147511-69-1 | >98.00% | |
Pitavastatin is a 3-Hydroxymethyl-3-glutaryl-CoA (HMG-CoA) reductase inhibitors. The IC 50 value of the HMG-CoA reductase activity in the Hep G2 cells for Pitavastatin was 5.8nM. | ||||
| GC11424 | Valproic acid | 99-66-1 | >98.00% | |
HDAC1 inhibitor | ||||
| GC11720 | 17-AAG (KOS953) | 75747-14-7 | >98.00% | |
17-AAG (KOS953) is a potent Hsp90 inhibitor (IC 50 =5nM). | ||||
| GC12017 | Isoniazid | 54-85-3 | >99.50% | |
antibiotic used for the treatment of tuberculosis | ||||
| GC12116 | Pitavastatin Calcium | 147526-32-7 | >99.00% | |
Enzyme HMGCR inhibitor | ||||
| GC12339 | Ivermectin | 70288-86-7 | >98.00% | |
Ivermectin is a macrolide endectocide with activity against both endoparasites and ectoparasites. | ||||
| GC12495 | Olanzapine | 132539-06-1 | >99.50% | |
Olanzapine is a monoamine antagonist. | ||||
| GC12807 | U0126-EtOH | 1173097-76-1 | >98.00% | |
U0126-EtOH is a non-ATP competitive and selective inhibitor of MEK1 and MEK2 with IC 50 values of 72nM and 58nM, respectively. | ||||
| GC13001 | SB 203580 hydrochloride | 869185-85-3 | >98.00% | |
Adezmapimod (SB 203580) hydrochloride is a selective and ATP-competitive p38 MAPK inhibitor with IC50s of 50 nM and 500 nM for SAPK2a/p38 and SAPK2b/p38β2, respectively. | ||||
| GC13443 | Doxazosin Mesylate | 77883-43-3 | >99.50% | |
α1-adrenergic receptor antagonist | ||||
| GC13554 | Deferoxamine mesylate | 138-14-7 | >98.00% | |
Deferoxamine mesylate is an iron chelator that binds Fe(III) and many other metal cations. | ||||
| GC13595 | SB 203580 | 152121-47-6 | >99.00% | |
SB 203580 is a specific inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) pathway . | ||||
| GC14191 | Ruxolitinib (INCB18424) | 941678-49-5 | >98.00% | |
Ruxolitinib (INCB018424), as an inhibitor, inhibits Janus-associated kinases (JAKs)JAK1 and JAK2 with IC 50 values of 3.3 nM and 2.8 nM, respectively. | ||||
| GC14553 | Resveratrol | 501-36-0 | >99.50% | |
Resveratrol (trans-Resveratrol; SRT501) is a phytoalexin. | ||||
| GC14591 | Hemin chloride | 16009-13-5 | >98.00% | |
Hemin chloride, a substrate of heme oxygenase (HO)-1, induces HO-1 expression on a variety of cells to exert anti-oxidant and anti-inflammatory roles. | ||||
| GC14787 | Curcumin | 458-37-7 | >98.00% | |
A yellow pigment with diverse biological activities | ||||
