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Cat No. | Product Name | Synonyms | Targets |
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T72403 | Ferroptosis inducer-1 | ||
Ferroptosis inducer-1 is a Ferroptosis inducer with antitumor potential . | |||
T82408 | Ferroptosis-IN-3 | Ferroptosis | |
Ferroptosis-IN-3 (Compound 25), a ferroptosis inhibitor, demonstrates potent activity by inhibiting RSL3-induced ferroptosis in HT-1080 cells (EC50: 8.6 nM). It exhibits radical scavenging abilities against DPPH and ABTS... | |||
T79945 | Ferroptosis-IN-1 | Ferroptosis | |
Ferroptosis-IN-1, a diterpene derived from A. campylantha, functions as a ferroptosis inhibitor with an EC50 of 10 μM and is utilized in the study of neuroinflammatory diseases [1]. | |||
T1710 | Trolox | Apoptosis , Antioxidant , Ferroptosis , Reactive Oxygen Species | |
Trolox is a vitamin E analogue, used in reducing oxidative stress or damage. | |||
T2376 | Liproxstatin-1 | Ferroptosis | |
Liproxstatin-1 is a potent and selective inhibitor of iron death (IC50=22 nM). Liproxstatin-1 protects cells from iron death induced by iron death inducers (e.g., Erastin, RSL3). | |||
T1765 | Erastin | Ferroptosis , VDAC | |
Erastin is an iron death activator that acts on the mitochondrial VDAC in a ROS- and iron-dependent manner. Erastin has anti-tumor activity and acts selectively on tumor cells with RAS-carcinogenic mutations. The product... | |||
T5343 | UAMC-3203 | UAMC 3203,UAMC3203 | Ferroptosis |
UAMC-3203 is a potent and selective Ferroptosis inhibitor (IC50: 12 nM). | |||
T4360 | ML385 | Others , Ferroptosis , Nrf2 | |
ML385 is an NRF2 inhibitor (IC50=1.9 μM) with novelty and specificity. ML385 has anti-inflammatory activity by modulating anti-oxidative stress through the inhibition of NRF2. ML385 also exhibits anti-tumor activity. | |||
T4066 | FIN56 | Ferroptosis | |
FIN56 is a specific inducer of ferroptosis. | |||
T1482 | Ciclopirox | HOE296b | ATPase , Ferroptosis , Antibacterial , Autophagy , Antifungal |
Ciclopirox (HOE296b) exerts its action by binding to and chelating trivalent cations, such as Fe3+ and Al3+, thereby inhibiting the availability of essential co-factors for enzymes. Ciclopirox is a synthetic, broad-spect... | |||
T6243 | U-73122 | U73122 | Phospholipase , Ferroptosis , Lipoxygenase |
U-73122 (U73122) , an effective PLC inhibitor, reduces agonist-induced Ca2+ increases in platelets and PMN. | |||
T37314 | JKE-1674 | GPX | |
JKE-1674 is an inhibitor of glutathione peroxidase 4 (GPX4). JKE-1674 is an active metabolite of the GPX4 inhibitor ML-210. | |||
T4309 | CIL56 | CA3 | Ferroptosis , ROS |
CIL56 (CA3) is a small molecule that induces cellular ferroptosis through the production of iron-dependent reactive oxygen species (ROS). It also induces accumulation of long-chain saturated, monounsaturated, and polyuns... | |||
T8970 | ML162 | Ferroptosis , GPX , Glutathione Peroxidase | |
ML162 is an inhibitor of GPX4 that is selectively lethal to mutant RAS oncogene-expressing cell lines (IC50s = 25 and 578 nM for HRASG12V-expressing and wild-type BJ fibroblasts, respectively) | |||
T9073 | SRS16-86 | Ferroptosis | |
SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of ferroptosis. | |||
T8662 | UAMC-3203 hydrochloride | Ferroptosis | |
UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM. | |||
T19467 | NADPH tetracyclohexanamine | NADPH (tetracyclohexanamine) | Ferroptosis |
NADPH tetracyclohexanamine (NADPH (tetracyclohexanamine)) is a cofactor and biological reducing agent. | |||
T7092 | NADPH tetrasodium salt | Others , Ferroptosis , Endogenous Metabolite | |
NADPH tetrasodium salt is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate, which acts as an electron donor in a variety of biological reactions. NADPH tetrasodium salt is also an end... | |||
T1787 | Levobupivacaine | Sodium Channel | |
Levobupivacaine is an amino-amide local anaesthetic drug belonging to the family of n-alkylsubstituted pipecoloxylidide. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by AstraZ... | |||
T11631 | IFSP1 | Ferroptosis | |
iFSP1, a potent, selective, and glutathione-independent ferroptosis suppressor protein 1 (FSP1) (AIFM2) inhibitor with an EC50 of 103 nM, sensitizes diverse human cancer cell lines to ferroptosis inducers like (1S,3R)-RS... | |||
T0935 | Butylated hydroxytoluene | BHT FCC/NF | Antioxidant , Ferroptosis |
Butylated hydroxytoluene (BHT FCC/NF) is an antioxidant widely used in food, cosmetics and industrial liquids. It is a ferroptosis inhibitor. | |||
T1565 | Deferiprone | Deferidone,CP20 | Others , HCV Protease , Ferroptosis , UGT |
Deferiprone (Deferidone) is an Iron Chelator. The mechanism of action of deferiprone is as an Iron Chelating Activity. | |||
T1564 | Cisplatin | cis-Diaminodichloroplatinum,CDDP | DNA Alkylator/Crosslinker , Ferroptosis , DNA/RNA Synthesis , Autophagy |
Cisplatin (CDDP) is a DNA cross-linking agent. Cisplatin has antitumor activity and inhibits DNA synthesis by forming DNA adducts in cancer cells. Cisplatin also activates iron death and induces autophagy. | |||
T2488 | BAY 87-2243 | Ferroptosis , HIF/HIF Prolyl-Hydroxylase , HIF | |
BAY 87-2243 is a potent and selective inhibitor of hypoxia-inducible factor-1 (HIF-1). | |||
T6099 | Setanaxib | GKT137831 | NADPH-oxidase , Ferroptosis , NADPH |
Setanaxib (GKT137831) is a potent, specific dual NADPH oxidase (NOX1/4) inhibitor. | |||
T8922 | SRS11-92 | AA9 | Ferroptosis |
SRS11-92 (AA9) is a ferroptosis inhibitor and a derivative of ferrostatin-1 | |||
T4414 | Eprenetapopt | APR-246,PRIMA-1Met | Apoptosis , Others , Ferroptosis , p53 , Autophagy |
Eprenetapopt (PRIMA-1Met) restores wild-type conformation and function to mutant p53, and triggers apoptosis in tumor cells. PRIMA-1MET also targets the selenoprotein thioredoxin reductase 1 (TrxR1), a key regulator of c... | |||
T6821 | Dp44mT | Apoptosis , Others , Ferroptosis | |
Dp44mT, a effective iron chelator, has selective antitumor activity. | |||
T0191 | Linagliptin | BI 1356 | Ferroptosis , Proteasome , DPP-4 , Autophagy |
Linagliptin (BI 1356) is a potent, orally bioavailable dihydropurinedione-based inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity. | |||
T6192 | Alogliptin | SYR-322 | Ferroptosis , Proteasome , DPP-4 |
Alogliptin (SYR-322)(SYR-322) is a potent, selective inhibitor of DPP-4 with IC50 of <10 nM, exhibits greater than 10, 000-fold selectivity over DPP-8 and DPP-9. | |||
T8375 | ML-210 | CID 49766530 | Ferroptosis , GPX , Glutathione Peroxidase , Ras |
ML-210 (CID 49766530) is a selective RAS and covalent glutathione peroxidase 4 (GPX4) inhibitor(GPX4, EC50 : 30 nM), with anti-cancer activity | |||
T5364 | TBHQ | tert-Butylhydroquinone | Apoptosis , ERK , Others , Ferroptosis , Nrf2 , Autophagy |
TBHQ (tert-Butylhydroquinone) is an antioxidant that induces an antioxidant response through the redox-sensitive transcription factor Nrf2. | |||
T1934 | Bay 11-7085 | BAY 11-7083 | Apoptosis , IκB/IKK , Ferroptosis , NF-κB |
Bay 11-7085 can irreversibly inhibit the IκBα phosphorylation induced by TNFα (IC50: 10 μM). | |||
T0477 | Zileuton | Abbott 64077,A 64077 | Ferroptosis , Lipoxygenase , COX |
Zileuton (A 64077) is a synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which catalyzes the formation of leukotrienes from arachidonic acid; ca... | |||
T1114 | Ciclopirox olamine | Ciclopirox ethanolamine | ATPase , Others , Ferroptosis , Antibacterial , Antifungal |
Ciclopirox olamine is a broad-spectrum antifungal agent with additional antibacterial and anti-inflammatory activities. | |||
T3646 | RSL3 | RSL3 1S,1S,3R-RSL3 | Ferroptosis , GPX , Glutathione Peroxidase |
RSL3 (RSL3 1S) is an inhibitor of GPX4, and inhibits system xc- that blocks GSH synthesis (IC50=100 nM). RSL3 is a VDAC-independent activator of iron death that is selective for tumor cells carrying oncogenic RAS. | |||
T1847 | Necrostatin-1 | Nec-1,Necrostatin 1 | Indoleamine 2,3-Dioxygenase (IDO) , Ferroptosis , Autophagy , RIP kinase |
Necrostatin-1 (Nec-1) is a necrotic apoptosis inhibitor and RIP1 inhibitor with specificity. Necrostatin-1 inhibits TNF-α-induced necrotic apoptosis. Necrostatin-1 also inhibits IDO. | |||
T6500 | Ferrostatin-1 | Ferrostatin 1,Ferrostatin-1 (Fer-1) | Ferroptosis , Antifungal |
Ferrostatin-1 (Fer-1) is a potent and selective inhibitor of iron death. Ferrostatin-1 potently inhibits Erastin-induced iron death in HT-1080 cells with an EC50 of 60 nM. Ferrostatin-1 also exhibits antioxidant and anti... | |||
T1457 | Deferasirox | ICL 670,CGP-72670 | Others , Ferroptosis , Antibacterial |
Deferasirox (CGP-72670) is an oral iron chelating agent used to treat chronic iron overload. | |||
T0907 | Sulfasalazine | NSC 667219,Azulfidine | Apoptosis , Ferroptosis , NF-κB , COX , Antibacterial , Antibiotic , Autophagy |
Sulfasalazine (Azulfidine) is a synthetic salicylic acid derivative with affinity for connective tissues containing elastin and formulated as a prodrug | |||
T7530 | PD146176 | NSC168807 | Ferroptosis , Lipoxygenase , Autophagy |
PD146176 (NSC-168807) is an inhibitor of 15-Lipoxygenase (15-LO) , it inhibits rabbit reticulocyte 15-LO with Ki of 197 nM and IC50 of 0.54 μM. PD146176 reverses cognitive impairment, brain amyloidosis, and tau pathology... | |||
T3109 | SP600125 | 1PMV,JNK Inhibitor II,Nsc75890,Pyrazolanthrone | Apoptosis , Ferroptosis , Trk receptor , JNK , Aurora Kinase , Autophagy |
SP600125 (JNK Inhibitor II) is a JNK inhibitor that inhibits JNK1, JNK2, and JNK3 (IC50=40/40/90 nM) with oral potency, reversibility, and ATP-competitive properties. SP600125 inhibits autophagy and induces apoptosis. | |||
T0214 | Pioglitazone | U 72107 | Ferroptosis , PPAR |
Pioglitazone (U 72107) is an insulin sensitizing agent and thiazolidinedione that is indicated for the treatment of type 2 diabetes. Pioglitazone has been linked to rare instances of acute liver injury. | |||
T27061 | CP-24879 hydrochloride | CP-24879 HCl | Others |
CP-24879 hydrochloride (CP-24879 HCl), a Δ5D/Δ6D dual-inhibitor, can significantly reduce intracellular lipid accumulation and inflammatory injury in hepatocytes. CP-24879 hydrochloride exhibits superior antisteatotic an... | |||
T0078 | Lapatinib | GSK572016,GW572016 | EGFR , Ferroptosis , Autophagy |
Lapatinib (GW572016) is an inhibitor of ErbB2 and EGFR (IC50=9.2/10.8 nM) with oral activity. Lapatinib has antitumor activity and can be used to treat advanced or metastatic breast cancer with HER2 overexpression. | |||
T1885 | Siramesine hydrochloride | Lu 28-179 hydrochloride | Ferroptosis , Sigma receptor , lysosomal autophagy |
Siramesine hydrochloride (Lu 28-179 hydrochloride) is a selective sigma-2 receptor agonist, which has been shown to trigger cell death of Y cells and to exhibit a potent anticancer activity in vivo. | |||
T0093L | Sorafenib | Bay 43-9006 | Apoptosis , Raf , VEGFR , FLT , Ferroptosis , PDGFR , c-Kit , Autophagy |
Sorafenib (Bay 43-9006) is a multikinase inhibitor that inhibits Raf-1, B-Raf, VEGFR2, VEGFR3, VEGFR4, PDGFRβ, FLT3, c-Kit, and others (IC50=6/22/90/15/20/20/57/58 nM) with oral activity. Sorafenib has antitumor activity... | |||
T3170 | Troglitazone | CS-045,Romozin,Rezulin,Romglizone,Noscal,Prelay | Apoptosis , Ferroptosis , PPAR , Autophagy |
Troglitazone (Romglizone) is a PPARγ agonist with anti-inflammatory and anti-tumor activity. | |||
T1622 | Rosiglitazone maleate | BRL 49653C,BRL 49653 | Ferroptosis , TRP/TRPV Channel , PPAR , Autophagy |
Rosiglitazone maleate (BRL 49653) is the maleate salt of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity. | |||
T6954 | PRIMA-1 | 2,2-Bis(hydroxymethyl)-3-quinuclidinone,NSC-281668,PRIMA 1 | Apoptosis , Others , Ferroptosis , Autophagy |
PRIMA-1 (NSC-281668) is a mutant p53 reactivator. It induces apoptosis and inhibits growth of human tumors with mutant p53. |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3S1447 | Arteannuin B | SARS-CoV , Ferroptosis | |
1. Arteannuin B has potent antimalarial activity. | |||
T2887 | Trigonelline | Trigenolline | Apoptosis , Others , Ferroptosis , Endogenous Metabolite |
Trigonelline (Trigenolline), an alkaloid with potential antidiabetic activity, is present in considerable amounts in coffee. | |||
T6468 | D-glutamine | Mitophagy , Ferroptosis , Endogenous Metabolite , GluR , Autophagy | |
D-glutamine, an D type stereoisomer of glutamine, is one of the 20 amino acids which is encoded by the standard genetic code. | |||
T5515 | Hemin | Hemin chloride | Mitophagy , Ferroptosis , Autophagy |
Hemin (Hemin chloride) is a chlorinated iron-containing porphyrin, a heme oxygenase (HO)-1 inducer. Hemin has therapeutic activity in porphyrias by reducing heme deficiency in patients, thereby inhibiting δ-aminolevulini... | |||
T2858 | Baicalein | 5,6,7-Trihydroxyflavone | Ferroptosis , Influenza Virus , ROS , Xanthine Oxidase |
Baicalein (5,6,7-Trihydroxyflavone) is a xanthine oxidase inhibitor. | |||
T0433 | Artesunate | WR-256283 | Virus Protease , Ferroptosis , STAT , Parasite |
Artesunate (WR-256283) is part of the artemisinin group of drugs that treat malaria. It is a semi-synthetic derivative of artemisinin that is water-soluble and may therefore be given by injection. It is on the World Heal... | |||
T5687 | WITHAFERIN A | Ferroptosis , NF-κB | |
WITHAFERIN A is a novel class of NFkappaB inhibitors, which hold promise as novel anti-inflammatory agents for treatment of various inflammatory disorders and/or cancer. | |||
T1207 | Lovastatin | MK-803,Mevinolin | Ferroptosis , HMG-CoA Reductase , Autophagy |
Lovastatin (MK-803) is an HMG-CoA Reductase Inhibitor, used for lowering cholesterol. | |||
TJS2190 | Nordihydroguaiaretic acid | NDGA,Dihydronorguaiaretic Acid | Antioxidant , Ferroptosis , Lipoxygenase , Autophagy |
Nordihydroguaiaretic acid (NDGA) (NDGA) is a phenolic antioxidant found in the leaves and twigs of the evergreen desert shrub, Larrea tridentata (Sesse and Moc. ex DC) Coville (creosote bush). It is a recognized inhibito... | |||
T6947 | Piperlongumine | PPLGM,Piplartine | Apoptosis , ERK , Ferroptosis , Reactive Oxygen Species , ROS , Antibacterial , Autophagy |
Piperlongumine (Piplartine) is a natural alkaloid from Piper longum L. It selectively kills cancer cells and strengthens the level of reactive oxygen species (ROS). | |||
T1922 | Pseudolaric Acid B | Apoptosis , p38 MAPK , Ferroptosis , HBV , Autophagy , Antifungal | |
Pseudolaric acid B, a natural diterpenoid compound, is isolated from Pseudolarix kaempferi. | |||
T2O2733 | L-Cystine | Cystine Acid,cystine | Antioxidant , Ferroptosis , Endogenous Metabolite |
L-Cystine (Cystine Acid) is not considered one of the 20 amino acids, L-Cystine (Cystine Acid) is a sulfur-containing derivative obtained from oxidation of cysteine amino acid thiol side chains. It functions as an antiox... | |||
THS1455 | DihydroarteMisinic acid | Dihydro-Artmisinic Acid | Ferroptosis , Parasite |
DihydroarteMisinic acid (Dihydro-Artmisinic Acid) is a natural product from Artemisia annua and the main direct precursor of artemisinin, which is a medicinal herb that is widely used to treat Malaria. | |||
T2856 | (-)-Epicatechin | L-Epicatechin,Epicatechin,(-)-Epicatechol | Ferroptosis , COX , Endogenous Metabolite |
(-)-Epicatechin (Epicatechin) is an inhibitor of cyclooxygenase-1 (COX-1), inhibiting the IL-1β-induced expression of iNOS by blocking the nuclear localization of the p65 subunit of NF-κB. | |||
T2796 | Coenzyme Q10 | Ubiquinone-10,CoQ10 | Ferroptosis , Reactive Oxygen Species , Endogenous Metabolite |
Coenzyme Q10 (CoQ10) (ubiquinone) is a naturally occurring compound, acting as the electron carrier in the mitochondrial respiratory chain. | |||
TJS1159 | Chrysosplenetin | Chrysosptertin B | P450 , Ferroptosis , P-gp |
Chrysosplenetin is a metabolic inhibitor of artemisinin. | |||
T0877 | Gallic acid | 3,4,5-Trihydroxybenzoic acid,Gallate,Benzoic acid | Apoptosis , Ferroptosis , Reactive Oxygen Species , ROS , COX , Endogenous Metabolite |
Gallic acid (Benzoic acid) is found in almost all plants. Plants known for their high gallic acid content include gallnuts,grapes,tea,hops and oak bark. | |||
T1644 | Dopamine hydrochloride | Dopamine HCl,ASL279 | Ferroptosis , Dopamine Receptor , 5-HT Receptor , Endogenous Metabolite |
Dopamine hydrochloride (ASL279) is a naturally occurring catecholamine formed by decarboxylation of dihydroxyphenylalanine and a precursor of norepinephrine and epinephrine. Dopamine hydrochloride binds to alpha-1- and b... | |||
T0326L | L-Glutamine | L-Glutamic acid 5-amide | Ferroptosis , Endogenous Metabolite , GluR |
L-Glutamine (L-Glutamic acid 5-amide) , a non-essential amino acid, is synthesized from glutamic acid and ammonia. | |||
T1297 | Eugenol | 4-Allylguaiacol,Allylguaiacol,4-Allyl-2-methoxyphenol,Eugenic acid | Apoptosis , Ferroptosis , Reactive Oxygen Species , Antibacterial , Parasite |
Eugenol (Allylguaiacol) is a Standardized Chemical Allergen. The physiologic effect of eugenol is by means of Increased Histamine Release and Cell-mediated Immunity. | |||
T0392 | Artemisinin | Qinghaosu,Artemisinine,Qinghaosu,NSC 369397,Artemisinine | HCV Protease , Ferroptosis , Akt , Parasite |
Artemisinin (Qinghaosu) is an ancient Chinese herbal therapy for malarial fevers which has been recently found to have potent activity against many forms of malarial organisms, including chloroquine-resistant Plasmodium ... | |||
T20819 | Ammonium iron(III) citrate | Ferric ammonium citrate | Others , Ferroptosis |
Ammonium iron(III) citrate (Ferric ammonium citrate) is a physiological form of non-ferritin-bound iron that causes intracellular iron overload leading to cellular iron death and enhances protein production. | |||
T0875 | Acetylcysteine | N-Acetyl-L-cysteine,LNAC,NAC | Apoptosis , TNF , Ferroptosis , Influenza Virus , Reactive Oxygen Species , ROS , Endogenous Metabolite |
Acetylcysteine (NAC) is an N-acetyl derivative of cysteine, a ROS inhibitor and mucolytic agent. Acetylcysteine induces apoptosis, can be used to reduce mucus thickness, and has anti-influenza viral activity. | |||
T0672 | Pravastatin sodium | CS-514 Sodium,CS-514 (sodium) | Ferroptosis , HMG-CoA Reductase , Autophagy |
Pravastatin sodium (CS-514 (sodium)), an HMG-CoA reductase inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM. | |||
T0326 | DL-Glutamine | Glutamin,DL-Gl,(±)-Glutamine,2-amino-4-carbamoylbutanoic acid | Ferroptosis , Amino Acids and Derivatives , Endogenous Metabolite |
DL-Glutamine (2-amino-4-carbamoylbutanoic acid), a non-essential amino acid, exists abundantly throughout the body and is participated in many metabolic processes. It is synthesized from glutamic acid and ammonia, and is... | |||
T5679 | (E)-Ferulic acid | trans-Ferulic acid,(E)-Coniferic acid | BCL , Ferroptosis , Wnt/beta-catenin , Endogenous Metabolite |
(E)-Ferulic acid ((E)-Coniferic 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 pr... | |||
TMA2394 | DL-alpha-Tocopherol | DL-α-Tocopherol,Alpha-Tochopherol,Ephanyl | Antioxidant , Ferroptosis |
DL-alpha-Tocopherol (Ephanyl) is a synthetic vitamin E that protects skin fibroblasts from the cytotoxic effects of UV light and has antioxidant properties. | |||
T0687 | Simvastatin | MK-0733,MK 733 | Apoptosis , Mitophagy , Ferroptosis , HMG-CoA Reductase , Autophagy |
Simvastatin (MK 733) is an HMG-CoA reductase inhibitor (Ki=0.2 nM) with oral activity. Simvastatin has hypolipidemic activity, inhibits hepatic production of cholesterol, and is also used for the prevention of cardiovasc... | |||
T2A2497 | L-Glutamic acid | (S)-Glutamic acid,glutamic acid,(+)-L-Glutamic acid,Aciglut,glutacid,Glutaminol | Apoptosis , Ferroptosis , Endogenous Metabolite , iGluR |
L-Glutamic acid (Glutaminol) acts as an excitatory transmitter, shows a direct activating effect on the release of DA from dopaminergic terminals. | |||
T1516 | Curcumin | Diferuloylmethane,Natural Yellow 3,Indian Saffron,Turmeric yellow | Mitophagy , Epigenetic Reader Domain , Ferroptosis , Influenza Virus , Nrf2 , Histone Acetyltransferase , HDAC , Autophagy |
Curcumin (Natural Yellow 3) is a phenolic natural product, an inhibitor of histone acetyltransferase p300/CREB (IC50=25 μM) with specificity. Curcumin has a wide range of pharmacological activities such as antitumor, ant... | |||
T2870 | Matrine | Vegard,Matridin-15-one,Matrinium,α-Matrine,(+)-Matrine | Mitophagy , Ferroptosis , Opioid Receptor , Autophagy |
Matrine (Vegard), an alkaloid isolated from the Sophora genus, acts as a kappa opioid receptor agonist. | |||
T6871 | L-Glutamic acid monosodium salt | Monosodium glutamate,Glutacyl,Glutavene,Ajinomoto,MSG | Apoptosis , Ferroptosis , GluR , iGluR |
L-Glutamic acid monosodium salt (MSG) (Monosodium glutamate) is an activator of mGlu1 receptor. | |||
T1085 | L-Glutathione reduced | GSH,Isethion,Glutathione,γ-L-Glutamyl-L-cysteinyl-glycine,Glutathion,Tathion | Ferroptosis , Reactive Oxygen Species , Endogenous Metabolite , Glutathione reductase |
L-Glutathione reduced (Glutathione) is a naturally occurring tripeptide found in cells as an endogenous antioxidant that scavenges oxygen free radicals. L-Glutathione reduced is a cofactor for certain enzymes and is invo... | |||
T1648 | α-Vitamin E | Dexrabeprazole Sodium,Vitamin E,Alpha-Tocopherol,D-α-Tocopherol,5,7,8-Trimethyltocol,(+)-alpha-Tocopherol | Others , Ferroptosis , Influenza Virus , Reactive Oxygen Species , Endogenous Metabolite , Antibacterial , PKC , GST |
α-Vitamin E (Dexrabeprazole Sodium) is a naturally-occurring form of vitamin E, a fat-soluble vitamin with potent antioxidant properties. | |||
TN5770 | Gingerenone A | Nrf2 | |
Gingerenone A is an effective Nrf2-Gpx4 activator. It is a small molecule compound isolated from ginger. It has anti-cancer activity, can prolong the cell cycle of cancer cells, and can inhibit dextran sodium sulfate (DS... | |||
T79940 | Moracin N | Glutathione Peroxidase | |
Moracin N, a ferroptosis inhibitor derived from mulberry leaves, exhibits neuroprotective activity by mitigating oxidative stress [1]. |
Cat No. | Product Name | ||
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L8700 | Ferroptosis Compound Library | 800 compounds | |
A unique collection of 800 ferroptosis signaling pathway related compounds, a powerful tool for new target identification, drug discovery, and mechanism study; | |||
L8710 | Cuproptosis Compound Library | 411 compounds | |
TargetMol’s Cuproptosis Compound Library is a collection of 411 compounds related to copper-dependent death that can be used to study its mechanism and related diseases. |