Ferroptosis
Ferroptosis is a unique iron-dependent form of nonapoptotic cell death. It is triggered by oncogenic RAS-selective lethal small molecule erastin. Acitvation of ferroptosis lead to nonapoptotic destruction of cancer cells.
Products Related to Ferroptosis(211)
- GC30512Vatiquinone (EPI-743)CAS: 1213269-98-7Purity: >98.00%
Vatiquinone (EPI-743) (Vatiquinone; α-Tocotrienol quinone; PTC-743; NCT04378075) is a potent cellular oxidative stress protectant, inhibits ferroptosis in cells, which could be used for the study for mitochondrial diseases.
- GC30788L-Glutamic acid monosodium salt (Monosodium glutamate)CAS: 142-47-2Purity: >99.50%
L-Glutamic acid monosodium salt (Monosodium glutamate) acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA).
- GC31492Vildagliptin dihydrate (LAF237 dihydrate)CAS: 2133364-01-7Purity: >98%
Vildagliptin dihydrate (LAF237 dihydrate) (LAF237 dihydrate) is a potent, stable, selective dipeptidyl peptidase IV (DPP-IV) inhibitor with an IC50 of 3.5 nM in human Caco-2 cells.
- GC31940Docebenone (AA 861)CAS: 80809-81-0Purity: >99.00%
Docebenone (AA 861) (AA 861) is a potent, selective and orally active 5-LO (5-lipoxygenase) inhibitor.
- GC32723CDDO-Im (RTA-403)CAS: 443104-02-7Purity: >98.00%
CDDO-Im (RTA-403) is a synthetic triterpenoid that activates Nuclear factor erythroid 2–related factor 2 (Nrf2) signaling by binding to Kelch-like ECH-associated protein 1 (Keap1), thereby inhibiting Nrf2 degradation and increasing its protein levels.
- GC33023D,L-Buthionine-(S,R)-sulfoximine (Buthionine sulfoximine)CAS: 5072-26-4Purity: >98.00%
D,L-Buthionine-(S,R)-sulfoximine (Butionine sulfoximine) is a potent inhibitor of glutamylcysteine synthetase biosynthesis.
- GC33098L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine)CAS: 83730-53-4Purity: >98.00%
L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine) is a glutathione synthesis inhibitor.
- GC33468Rehmannioside ACAS: 81720-05-0Purity: >98.00%
Rehmannioside A is an inhibitor of cytochrome P450 enzymes (CYP3A4, 2C9, and 2D6), with IC 50 values of 10.08, 12.62, and 16.43μM, respectively.
- GC34057TBHQ (tert-Butylhydroquinone)CAS: 1948-33-0Purity: >99.50%
TBHQ(tert-Butylhydroquinone) is a powerful phenolic antioxidant capable of reducing oxidative stress and inflammatory reactions.
- GC34058NADPH tetrasodium saltCAS: 2646-71-1Purity: >98.00%
NADPH tetrasodium salt is a sodium salt form of reduced nicotinamide adenine dinucleotide phosphate (NADPH), which is an essential cofactor in cells and acts as an electron donor.
- GC34980(E)-Ferulic acidCAS: 537-98-4Purity: >99.00%
(E)-Ferulic acid is a isomer of Ferulic acid which is an aromatic compound, abundant in plant cell walls. (E)-Ferulic acid causes the phosphorylation of β-catenin, resulting in proteasomal degradation of β-catenin and increases the expression of pro-apoptotic factor Bax and decreases the expression of pro-survival factor survivin. (E)-Ferulic acid shows a potent ability to remove reactive oxygen species (ROS) and inhibits lipid peroxidation. (E)-Ferulic acid exerts both anti-proliferation and anti-migration effects in the human lung cancer cell line H1299.
- GC35398Arteannuin BCAS: 50906-56-4Purity: >98.00%
Arteannuin B co-occurs with artemisinin, which is the potent antimalarial principle of the Chinese medicinal herb Artemisia annua (Asteraceae).
- GC35876DL-GlutamineCAS: 6899-04-3Purity: >98.00%
DL-Glutamine is used for biochemical research and drug synthesis.
- GC36011Ethylenediaminetetraacetic acid trisodium saltCAS: 150-38-9Purity: >98.00%
Ethylenediaminetetraacetic acid trisodium salt (EDTA trisodium salt) is used to bind metal ions in the practice of chelation therapy, for treating mercury and lead poisoning, used in a similar manner to remove excess iron from the body, for treating the complication of repeated blood transfusions, as would be applied to treat thalassaemia.
- GC37664Sorafenib (D3)CAS: 1130115-44-4Purity: >99.00%
An internal standard for the quantification of sorafenib
- GC37665Sorafenib (D4)CAS: 1207560-07-3Purity: >98%
Sorafenib (D4) (Bay 43-9006-d4) is the deuterium labeled Sorafenib. Sorafenib is a multikinase inhibitor IC50s of 6 nM, 20 nM, and 22 nM for Raf-1, B-Raf, and VEGFR-3, respectively.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC30512 | Vatiquinone (EPI-743) | 1213269-98-7 | >98.00% | |
Vatiquinone (EPI-743) (Vatiquinone; α-Tocotrienol quinone; PTC-743; NCT04378075) is a potent cellular oxidative stress protectant, inhibits ferroptosis in cells, which could be used for the study for mitochondrial diseases. | ||||
| GC30788 | L-Glutamic acid monosodium salt (Monosodium glutamate) | 142-47-2 | >99.50% | |
L-Glutamic acid monosodium salt (Monosodium glutamate) acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). | ||||
| GC31492 | Vildagliptin dihydrate (LAF237 dihydrate) | 2133364-01-7 | >98% | |
Vildagliptin dihydrate (LAF237 dihydrate) (LAF237 dihydrate) is a potent, stable, selective dipeptidyl peptidase IV (DPP-IV) inhibitor with an IC50 of 3.5 nM in human Caco-2 cells. | ||||
| GC31940 | Docebenone (AA 861) | 80809-81-0 | >99.00% | |
Docebenone (AA 861) (AA 861) is a potent, selective and orally active 5-LO (5-lipoxygenase) inhibitor. | ||||
| GC32237 | CIL56 | 300802-28-2 | >98% | |
An inducer of non-apoptotic cell death; YAP1 (YES related protein 1) targeted inhibitor | ||||
| GC32723 | CDDO-Im (RTA-403) | 443104-02-7 | >98.00% | |
CDDO-Im (RTA-403) is a synthetic triterpenoid that activates Nuclear factor erythroid 2–related factor 2 (Nrf2) signaling by binding to Kelch-like ECH-associated protein 1 (Keap1), thereby inhibiting Nrf2 degradation and increasing its protein levels. | ||||
| GC33023 | D,L-Buthionine-(S,R)-sulfoximine (Buthionine sulfoximine) | 5072-26-4 | >98.00% | |
D,L-Buthionine-(S,R)-sulfoximine (Butionine sulfoximine) is a potent inhibitor of glutamylcysteine synthetase biosynthesis. | ||||
| GC33098 | L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine) | 83730-53-4 | >98.00% | |
L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine) is a glutathione synthesis inhibitor. | ||||
| GC33468 | Rehmannioside A | 81720-05-0 | >98.00% | |
Rehmannioside A is an inhibitor of cytochrome P450 enzymes (CYP3A4, 2C9, and 2D6), with IC 50 values of 10.08, 12.62, and 16.43μM, respectively. | ||||
| GC33469 | NADPH tetracyclohexanamine | 100929-71-3 | >98% | |
A reduced form of NADP + | ||||
| GC34057 | TBHQ (tert-Butylhydroquinone) | 1948-33-0 | >99.50% | |
TBHQ(tert-Butylhydroquinone) is a powerful phenolic antioxidant capable of reducing oxidative stress and inflammatory reactions. | ||||
| GC34058 | NADPH tetrasodium salt | 2646-71-1 | >98.00% | |
NADPH tetrasodium salt is a sodium salt form of reduced nicotinamide adenine dinucleotide phosphate (NADPH), which is an essential cofactor in cells and acts as an electron donor. | ||||
| GC34070 | Brusatol | 14907-98-3 | >98.00% | |
Brusatol is an Nrf2 inhibitor isolated from Brucea javanica and exhibits significant tumor inhibition in multiple cancers through decreased resistance to cancer oxidative stress injury. | ||||
| GC34939 | UAMC-3203 hydrochloride | 2271358-65-5 | >98.50% | |
A ferroptosis inhibitor | ||||
| GC34980 | (E)-Ferulic acid | 537-98-4 | >99.00% | |
(E)-Ferulic acid is a isomer of Ferulic acid which is an aromatic compound, abundant in plant cell walls. (E)-Ferulic acid causes the phosphorylation of β-catenin, resulting in proteasomal degradation of β-catenin and increases the expression of pro-apoptotic factor Bax and decreases the expression of pro-survival factor survivin. (E)-Ferulic acid shows a potent ability to remove reactive oxygen species (ROS) and inhibits lipid peroxidation. (E)-Ferulic acid exerts both anti-proliferation and anti-migration effects in the human lung cancer cell line H1299. | ||||
| GC35398 | Arteannuin B | 50906-56-4 | >98.00% | |
Arteannuin B co-occurs with artemisinin, which is the potent antimalarial principle of the Chinese medicinal herb Artemisia annua (Asteraceae). | ||||
| GC35399 | Artefenomel | 1029939-86-3 | >99.00% | |
An antimalarial agent | ||||
| GC35692 | Chrysosplenetin | 603-56-5 | >99.50% | |
A flavonoid with diverse biological activities | ||||
| GC35795 | D,L-Buthionine-(S,R)-sulfoximine hydrochloride | - | >99.00% | |
| GC35876 | DL-Glutamine | 6899-04-3 | >98.00% | |
DL-Glutamine is used for biochemical research and drug synthesis. | ||||
| GC36011 | Ethylenediaminetetraacetic acid trisodium salt | 150-38-9 | >98.00% | |
Ethylenediaminetetraacetic acid trisodium salt (EDTA trisodium salt) is used to bind metal ions in the practice of chelation therapy, for treating mercury and lead poisoning, used in a similar manner to remove excess iron from the body, for treating the complication of repeated blood transfusions, as would be applied to treat thalassaemia. | ||||
| GC36926 | Piperazine Erastin | 1538593-71-3 | >98% | |
| GC37664 | Sorafenib (D3) | 1130115-44-4 | >99.00% | |
An internal standard for the quantification of sorafenib | ||||
| GC37665 | Sorafenib (D4) | 1207560-07-3 | >98% | |
Sorafenib (D4) (Bay 43-9006-d4) is the deuterium labeled Sorafenib. Sorafenib is a multikinase inhibitor IC50s of 6 nM, 20 nM, and 22 nM for Raf-1, B-Raf, and VEGFR-3, respectively. | ||||
