GLPBio

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)

  • GC30512 structure
    GC30512Vatiquinone (EPI-743)
    CAS: 1213269-98-7
    Purity: >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 structure
    GC30788L-Glutamic acid monosodium salt (Monosodium glutamate)
    CAS: 142-47-2
    Purity: >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 structure
    GC31492Vildagliptin dihydrate (LAF237 dihydrate)
    CAS: 2133364-01-7
    Purity: >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 structure
    GC31940Docebenone (AA 861)
    CAS: 80809-81-0
    Purity: >99.00%

    Docebenone (AA 861) (AA 861) is a potent, selective and orally active 5-LO (5-lipoxygenase) inhibitor.

  • GC32237 structure
    GC32237CIL56
    CAS: 300802-28-2
    Purity: >98%

    An inducer of non-apoptotic cell death; YAP1 (YES related protein 1) targeted inhibitor

  • GC32723 structure
    GC32723CDDO-Im (RTA-403)
    CAS: 443104-02-7
    Purity: >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 structure
    GC33023D,L-Buthionine-(S,R)-sulfoximine (Buthionine sulfoximine)
    CAS: 5072-26-4
    Purity: >98.00%

    D,L-Buthionine-(S,R)-sulfoximine (Butionine sulfoximine) is a potent inhibitor of glutamylcysteine synthetase biosynthesis.

  • GC33098 structure
    GC33098L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine)
    CAS: 83730-53-4
    Purity: >98.00%

    L-Buthionine-(S,R)-sulfoximine (L-Butionine sulfoximine) is a glutathione synthesis inhibitor.

  • GC33468 structure
    GC33468Rehmannioside A
    CAS: 81720-05-0
    Purity: >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 structure
    GC33469NADPH tetracyclohexanamine
    CAS: 100929-71-3
    Purity: >98%

    A reduced form of NADP +

  • GC34057 structure
    GC34057TBHQ (tert-Butylhydroquinone)
    CAS: 1948-33-0
    Purity: >99.50%

    TBHQ(tert-Butylhydroquinone) is a powerful phenolic antioxidant capable of reducing oxidative stress and inflammatory reactions.

  • GC34058 structure
    GC34058NADPH tetrasodium salt
    CAS: 2646-71-1
    Purity: >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 structure
    GC34070Brusatol
    CAS: 14907-98-3
    Purity: >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 structure
    GC34939UAMC-3203 hydrochloride
    CAS: 2271358-65-5
    Purity: >98.50%

    A ferroptosis inhibitor

  • GC34980 structure
    GC34980(E)-Ferulic acid
    CAS: 537-98-4
    Purity: >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 structure
    GC35398Arteannuin B
    CAS: 50906-56-4
    Purity: >98.00%

    Arteannuin B co-occurs with artemisinin, which is the potent antimalarial principle of the Chinese medicinal herb Artemisia annua (Asteraceae).

  • GC35399 structure
    GC35399Artefenomel
    CAS: 1029939-86-3
    Purity: >99.00%

    An antimalarial agent

  • GC35692 structure
    GC35692Chrysosplenetin
    CAS: 603-56-5
    Purity: >99.50%

    A flavonoid with diverse biological activities

  • GC35795 structure
  • GC35876 structure
    GC35876DL-Glutamine
    CAS: 6899-04-3
    Purity: >98.00%

    DL-Glutamine is used for biochemical research and drug synthesis.

  • GC36011 structure
    GC36011Ethylenediaminetetraacetic acid trisodium salt
    CAS: 150-38-9
    Purity: >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 structure
    GC36926Piperazine Erastin
    CAS: 1538593-71-3
    Purity: >98%
  • GC37664 structure
    GC37664Sorafenib (D3)
    CAS: 1130115-44-4
    Purity: >99.00%

    An internal standard for the quantification of sorafenib

  • GC37665 structure
    GC37665Sorafenib (D4)
    CAS: 1207560-07-3
    Purity: >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.