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Cat. No.	Product Name	Target	Signaling Pathways
T1765	Erastin	Ferroptosis; VDAC	Apoptosis; Membrane transporter/Ion channel
	Erastin 是一种作用于线粒体 VDAC 的铁死亡激活剂，具有 ROS 和铁依赖性。Erastin 具有抗肿瘤活性，选择性作用于 RAS 致癌突变的肿瘤细胞。该产品在溶液中不稳定，建议现配现用。
T16540	Piperazine Erastin	Ferroptosis	Apoptosis
	Piperazine Erastin 是erastin 的类似物。它会导致一种铁依赖形式的非凋亡性细胞死亡，称为铁死亡。
T5523	Imidazole ketone erastin IKE	Ferroptosis	Apoptosis
	Imidazole ketone erastin (IKE) 是一种铁死亡诱导剂，对 system Xc-胱氨酸/谷氨酸转运蛋白具有抑制作用。Imidazole ketone erastin 具有抗肿瘤活性，可以诱导谷胱甘肽耗竭和脂质过氧化。
T35994	Erastin2 Erastin2
	Erastin2 is a ferroptosis inducer and an inhibitor of the system xc- cystine/glutamate transporter.[1] [2] It inhibits glutamate release in CCF-STTG1 cells (IC50 = 0.0035 &#181M).[2] It induces cell death in HAP1 cells when used at a concentration of 5 &#181M, an effect that can be blocked by the ferroptosis inhibitor ferrostatin-1 or deferoxamine . [1] Erastin2 also induces ferroptotic cell death in HT-1080 cells (EC50 = 0.15 &#181M), an effect that can be blocked by the reducing agent β-merc...
T1787	Levobupivacaine	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine 是一种氨基酰胺类局麻药，属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。
T6566	Levobupivacaine hydrochloride Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) 是有效的钠通道阻滞剂。
T13619	Cloperastine fendizoate Hustazol	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Cloperastine fendizoate (Hustazol) 是 hERG K+ 电流的抑制剂，IC50 为 27 nM。
T25875	Noberastine R64947,T25875,R-64947,R 64947	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Noberastine (R 64947) 是一种新型组胺 H1拮抗剂，具有强效和特异性的外周抗组胺活性。
T0723	Cloperastine hydrochloride HT-11 hydrochloride,盐酸氯哌斯丁	Potassium Channel; 5-HT Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Cloperastine hydrochloride (HT-11 hydrochloride) 是 hERG K+电流的抑制剂，IC50为 27 nM，具有浓度依赖性。
T70773	Noberastine citrate
	Noberastine citrate, a histamine H1 antagonist, has potent and specific peripheral antihistaminic activity. Noberastine, a furan derivative of nor-astemizole (an astemizole metabolite), has been shown to have a more rapid onset, and shorter duration of action than astemizole with peak antihistaminic activity at 4h following ingestion. Noberastine is rapidly absorbed and the peak plasma levels are obtained within 2 h of oral dosing. In preclinical studies Noberastine has been shown to lack centra...
T33927	Perastine
	Perastine is a biochemical.
T71425	Noberastine maleate
	Noberastine maleate, a histamine H1 antagonist, has potent and specific peripheral antihistaminic activity. Noberastine, a furan derivative of nor-astemizole (an astemizole metabolite), has been shown to have a more rapid onset, and shorter duration of action than astemizole with peak antihistaminic activity at 4h following ingestion. Noberastine is rapidly absorbed and the peak plasma levels are obtained within 2 h of oral dosing. In preclinical studies Noberastine has been shown to lack centra...
T68889	Esterastin
	Esterastin is an Inhibitor of esterases.
T36404L	PRLX-93936 HCL PRLX-93936 hcl(903499-49-0 Free base)	Ferroptosis; Reactive Oxygen Species	Apoptosis; Immunology/Inflammation; Metabolism; NF-κB
	PRLX-93936 HCL 是 erastin 的类似物，并显示出与顺铂对非小细胞肺癌 (NSCLC) 细胞的协同作用。
T2376	Liproxstatin-1	Ferroptosis	Apoptosis
	Liproxstatin-1 是一种铁死亡抑制剂 (IC50=22 nM)，具有强效性和选择性。Liproxstatin-1 可以保护细胞免受铁死亡诱导剂 (如 Erastin、RSL3) 诱导的铁死亡。
T6500	Ferrostatin-1 Ferrostatin 1,Ferrostatin-1 (Fer-1)	Ferroptosis; Antifungal	Apoptosis; Microbiology/Virology
	Ferrostatin-1 (Fer-1) 是一种铁死亡抑制剂，具有强效性和选择性。Ferrostatin-1 有效抑制 Erastin 诱导的 HT-1080 细胞铁死亡 (EC50=60 nM)。Ferrostatin-1 还具抗氧化和抗真菌活性。
T8922	SRS11-92 AA9	Ferroptosis	Apoptosis
	SRS11-92 (AA9) 是一种铁死亡抑制剂和 Ferrostatin-1 的衍生物。它抑制 Erastin 诱导的 HT-1080 人纤维肉瘤细胞铁致细胞死亡，EC50为6 nM。
T36003	1(R)-(Trifluoromethyl)oleyl alcohol
	1(R)-(Trifluoromethyl)oleyl alcohol is an analog of oleic acid .1It inhibits ferroptosis induced by erastin in primary fibroblasts isolated from patients with Friedreich ataxia, a neuro- and cardiodegenerative disorder characterized by loss or impaired activity of frataxin (FXN), when used at concentrations of 5, 10, or 20 μM. 1(R)-(Trifluoromethyl)oleyl alcohol (5 μM) reduces lipid peroxidation induced byFXNsiRNA knockdown in NBT human myoblasts. 1.Cotticelli, M.G., Forestieri, R., Xia, S., et ...
T74461	Chalcones A-N-5
	ChalconesA-N-5, 一种三羟基查耳酮衍生物化合物，浓度低于100 µM (IC50> 1 mM) 时无细胞毒性，能显着促进细胞增殖。此外，ChalconesA-N-5 能促进受损脑组织中神经元的生长，抑制RSL或erastin诱导的铁死亡，并降低Aβ1-42蛋白聚集引发的脂质过氧化水平。因此，ChalconesA-N-5 作为分子骨架的候选物，对于开发用以研究AD的体内试验先导化合物具有重要潜力。
T36404	PRLX-93936
	PRLX-93936 is an analog of erastin that has antitumor activity. It inhibits the hypoxia-inducible factor 1 (HIF-1) signaling pathway under hypoxic conditions (IC50 = 0.09 μM in a cell-based reporter assay). PRLX-93936 (1 μM) also inhibits hypoxia-induced increases in HIF-1α expression in ME-180 cervical cancer cells. It inhibits the growth of HT-1080 fibrosarcoma, OVCAR-5 ovarian cancer, BJELR tumorigenic primary fibroblast, and PANC-1 pancreatic cancer cells with IC50 values of less than 100 nM...
T37248	Pantothenate Kinase Inhibitor
	Pantothenate Kinase Inhibitor (PANKi) is a reversible inhibitor of pantothenate kinase (PanK; IC50s = 70, 92, and 25 nM for PanK1β, PanK2, and PanK3, respectively), the rate-limiting enzyme in the synthesis of coenzyme A .1It binds to the ATP-PanK3 complex with an apparent binding constant of 300 nM and exhibits mixed-type inhibition with respect to ATP and pantothenate. PANKi inhibits CoA biosynthesis in C3A cells (IC50= 0.9 μM) with no effect on cell viability when used at concentrations up to...

化合物

Cat.No: T1765

Target: Ferroptosis, VDAC

Piperazine Erastin

Cat.No: T16540

Target: Ferroptosis

Imidazole ketone erastin

Cat.No: T5523

Synonym: IKE

Target: Ferroptosis

Cat.No: T35994

Synonym: Erastin2

Levobupivacaine

Cat.No: T1787

Target: Sodium Channel

Levobupivacaine hydrochloride

Cat.No: T6566

Synonym: Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride

Target: Sodium Channel

Cloperastine fendizoate

Cat.No: T13619

Synonym: Hustazol

Target: EGFR

Cat.No: T25875

Synonym: R64947,T25875,R-64947,R 64947

Target: Histamine Receptor

Cloperastine hydrochloride

Cat.No: T0723

Synonym: HT-11 hydrochloride,盐酸氯哌斯丁

Target: Potassium Channel, 5-HT Receptor

Noberastine citrate

Cat.No: T70773

Cat.No: T33927

Noberastine maleate

Cat.No: T71425

Cat.No: T68889

Cat.No: T36404L

Synonym: PRLX-93936 hcl(903499-49-0 Free base)

Target: Ferroptosis, Reactive Oxygen Species

Cat.No: T2376

Target: Ferroptosis

Cat.No: T6500

Synonym: Ferrostatin 1,Ferrostatin-1 (Fer-1)

Target: Ferroptosis, Antifungal

Cat.No: T8922

Synonym: AA9

Target: Ferroptosis

1(R)-(Trifluoromethyl)oleyl alcohol

Cat.No: T36003

Chalcones A-N-5

Cat.No: T74461

Cat.No: T36404

Pantothenate Kinase Inhibitor

Cat.No: T37248

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