Ferroptosis(铁死亡)
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 for Ferroptosis
- Cat.No. 产品名称 Information
- GC91783 FA16 FA16 is a ferroptosis inducer and an inhibitor of the system xc- cystine/glutamate transporter.
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GC91691
viFSP1
Versatile Inhibitor of Ferroptosis Suppressor Protein 1,Versatile Inhibitor of FSP1
viFSP1 is a species-independent inhibitor of ferroptosis suppressor protein 1 (FSP1; IC50s = 34 and 83 nM for the human and mouse enzymes, respectively). - GC91623 Ferroptosis Inducer 24 Ferroptosis inducer 24 is an inducer of ferroptosis.
- GC91613 FerroLOXIN-1 FerroLOXIN-1 is an inhibitor of the 15-lipoxygenase-2 (15-LO-2) and phosphatidylethanolamine-binding protein 1 (PEBP1) catalytic complex.
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GC91598
GPX4 16
Glutathione Peroxidase 4 16
GPX4 16 is an inhibitor of glutathione peroxidase 4 (GPX4). - GC71840 L-Cystine-34S2 L-Cystine-34S2是34S标记的L-胱氨酸。
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GC71839
L-Cystine-d4
L-Cystine-d4是氘标记的L-胱氨酸。
- GC71837 L-Glutamine-13C5,15N2,d5 L-Glutamine-13C5,15N2,d5是氘、13C-和15-标记的L-谷氨酰胺。
- GC71730 L-Glutathione reduced-13C2,15N L-Glutathione reduced-13C2,15N13C和15N标记的L-谷胱甘肽是否减少。
- GC70824 Pioglitazone-d4 (alkyl) Pioglitazone-d4 (alkyl)(U 72107-d4(烷基))是氘标记的吡格列酮。
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GC91380
N6F11
N6F11 is a novel, selective and potent inducer of iron death with anticancer and antitumour activity that promotes GPX4 degradation by binding to TRIM25 in cancer cells.
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GC91157
C18
一种共价的GPX4抑制剂
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GC90827
GPX4 24
Glutathione Peroxidase 4 24, PHGPx 24, Phospholipid Hydroperoxide Glutathione Peroxidase 24
一种GPX4抑制剂
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GC90714
LOC1886
一种GPX4抑制剂
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GC90713
FSEN1
Ferroptosis Sensitizer 1
FSP1的抑制剂
- GC70157 YL-939 YL-939 是一种有效的铁死亡 (ferroptosis) 抑制剂。 YL-939 通过靶向 PHB2/铁蛋白/铁轴来抑制铁死亡。
- GC68580 84-B10 84-B10 是一种 3-苯基戊二酸衍生物。84-B10 抑制 cisplatin 诱导的肾小管铁死亡。84-B10 减轻 cisplatin 诱导的线粒体损伤和氧化应激。84-B10 改善 cisplatin 诱导的急性肾损伤 (AKI)。
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GC68479
MMRi62
MMRi62 是一种铁死亡 (Ferroptosis) 诱导剂,靶向 MDM2-MDM4 (抑癌基因 p53 负调控因子)。MMRi62 对胰腺导管腺癌 (PDAC) 细胞显示出 p53 独立的促凋亡 (Apoptosis) 活性,并诱导其自噬 (Autophagy)。MMRi62 诱导铁死亡,伴随着活性氧增加和铁蛋白重链 (FTH1) 溶酶体降解。MMRi62 还可导致突变型 p53 的蛋白酶体降解,并对具有 KRAS 和 TP53 高频突变特征的原位异种移植 PDAC 小鼠模型具有体内药效。
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GC52413
5-Aminosalicylic Acid-d7
5-ASA-d7, Mesalamine-d7, Mesalazine-d7
An internal standard for the quantification of 5-aminosalicylic acid - GC52317 BCP-T.A. A ferroptosis inducer
- GC52290 (R)-HTS-3 An inhibitor of LPCAT3
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GC20109
Cefotiam hexetil hydrochloride
盐酸头孢替安酯; CTM-HE hydrochloride; SCE-2174 hydrochloride
Cefotiam hexetil hydrochloride 是可口服的第三代头孢菌素,是 cefotiam 的前药,但无抗菌作用。Cefotiam 是一种抗生素。
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GC52190
Imidazole Ketone Erastin
IKE
Imidazole Ketone Erastin是一种有效的、代谢稳定的系统xc- 抑制剂和铁凋亡诱导剂。 -
GC52164
Cu-ATSP
copper-ATSP, CuII(atsp)
A copper-containing bis(thiosemicarbazone) complex -
GC65163
Ardisiacrispin B
百两金皂苷B
Ardisiacrispin B在多因素耐药癌细胞中显示细胞毒性作用,通过铁中毒和凋亡细胞死亡。 -
GC65095
L-Glutamic acid-d5
L-谷氨酸 d5
L-Glutamic acid-d5 是 L-Glutamic acid 的氘代物。L-Glutamic acid 作为一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型(代谢型红藻氨酸、NMDA 和 AMPA)的激动剂。对 DA 从多巴胺能神经末梢释放的过程有激动作用。 -
GC65068
L-Glutamine 15N
L-Glutamic acid 5-amide 15N
L-Glutamine-15N (L-Glutamic acid 5-amide-15N) 是 15N 标记的 L-Glutamine。L-Glutamine (L-Glutamic acid 5-amide) 是在人体中大量存在且参与许多代谢过程的非必需氨基酸。L-Glutamine 为某些细胞中的氧化提供了碳源。 -
GC19936
Quisinostat dihydrochloride
QUISINOSTAT二盐酸盐,JNJ-26481585 dihydrochloride
A pan-HDAC inhibitor -
GC49868
D-α-Tocopheryl Quinone
α-Tocopherylquinone
An oxidative metabolite of vitamin E -
GC64352
L-Glutamic acid-15N
L-谷氨酸 15N
L-Glutamic acid-15N 是一种 15N 标记的 L-Glutamic acid。L-Glutamic acid 作为一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型(代谢型红藻氨酸、NMDA 和 AMPA)的激动剂。对 DA 从多巴胺能神经末梢释放的过程有激动作用。 -
GC49730
1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE-d11
15(S)-HETE-SAPE-d11, 15(S)-Hydroxyeicosatetraenoic Acid-SAPE-d11, 1-Stearoyl-2-15(S)-HETE-sn-glycero-3-Phosphatidylethanolamine-d11
An internal standard for the quantification of 1-stearoyl-2-15(S)-HETE-sn-glycero-3-PE -
GC49697
GPX4 Inhibitor 26a
Glutathione Peroxidase 4 Inhibitor 26a
A GPX4 inhibitor - GC49691 PSP A two-photon fluorescent probe for H2Sn
- GC49560 L6H21 An inhibitor of the MD-2 and TLR4 interaction
- GC49454 Complex 3 A fluorescent copper complex with anticancer activity
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GC49308
Ungeremine
石蒜碱内铵盐
A betaine-type alkaloid with diverse biological activities -
GC49058
DTPA
二乙烯三胺五醋酸,Diethylenetriaminepentaacetic acid; DTPA
A cell-impermeable metal chelating agent - GC49034 1(R)-(Trifluoromethyl)oleyl alcohol An oleic acid analog
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GC62643
L-Buthionine-(S,R)-sulfoximine hydrochloride
L-Buthionine sulfoximine hydrochloride; L-BSO hydrochloride
An irreversible inhibitor of the γ-glutamylcysteine synthetase -
GC62033
3α-Hydroxy pravastatin sodium
3Α-羟基普伐他汀钠
A metabolite of pravastatin -
GC61895
Ammonium iron(III) citrate
柠檬酸铁 (III) 铵; Ammonium ferric citrate; FAC
Ammonium ferric citrate (Ferric ammonium citrate, Ammonium iron(III) citrate, Iron ammonium citrate, FerriSeltz) induces ferroptosis in non-small-cell lung carcinoma through the inhibition of GPX4-GSS/GSR-GGT axis activity. -
GC61436
Gallic acid hydrate
没食子酸-水合物; 3,4,5-Trihydroxybenzoic acid hydrate
A phenol with diverse biological activities -
GC19706
Propacetamol hydrochloride
盐酸丙帕他莫
A prodrug form of acetaminophen - GC48954 CP21 An iron chelator
- GC48650 DTUN A lipophilic hyponitrite radical initiator
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GC48059
Rosiglitazone-d3
罗格列酮 d3
An internal standard for the quantification of rosiglitazone -
GC48030
RC574
An inhibitor of ferroptosis
- GC48029 RC363 An inhibitor of ferroptosis
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GC47870
Pantothenate Kinase Inhibitor
3-(2,4-二甲基吡啶并[2',3':3,4]吡唑并[1,5-A]嘧啶-3-基)-N-(3-(甲硫基)苯基)丙酰胺
A reversible inhibitor of pantothenate kinase - GC47478 JKE-1716 A GPX4 inhibitor