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Anti-infection

Antibiotic Arenavirus Bacterial CMV Enterovirus Filovirus Fungal HBV HCV HCV Protease HIV HIV Integrase HIV Protease HSV Influenza Virus Orthopoxvirus Parasite TMV Reverse Transcriptase RSV SARS-CoV Virus Protease RABV HPV DENV RABV
Apoptosis

Apoptosis Bcl-2 Family Caspase c-Myc DAPK Ferroptosis FKBP IAP Family MDM-2/p53 PKD Necroptosis Pyroptosis RIP kinase Thymidylate Synthase TNF Receptor TRADD Cuproptosis DAPK
Autophagy

Autophagy FKBP LRRK2 Mitophagy OGA ULK Beclin1 Atg4
Cell Cycle/DNA Damage

Antifolate APC ATM/ATR Aurora Kinase BMI-1 Casein Kinase CDK Checkpoint Kinase (Chk) CRISPR/Cas9 Deubiquitinase DNA Alkylator/Crosslinker DNA/RNA Synthesis DNA-PK Early 2 Factor (E2F) Eukaryotic Initiation Factor (eIF) GAK G-quadruplex Haspin Kinase HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 DNA Stain Nucleoside Antimetabolite/Analog p97 PAK PARP PERK PFKFB3 Polo-like Kinase (PLK) PPAR RAD51 Cyclin G-associated Kinase (GAK) ROCK ATF6 Haspin Kinase Sirtuin SRPK PDI Telomerase TOPK Topoisomerase Wee1 YB-1 poly (ADP ribose) glycohydrolase (PARG) OGG1
Cytoskeletal Signaling

Arp2/3 Complex Dynamin Gap Junction Protein Integrin Kinesin Microtubule/Tubulin Mps1 Myosin PAK ROCK
Epigenetics

AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain HDAC Histone Acetyltransferase Histone Demethylase Histone Methyltransferase MicroRNA PARP PKC Protein Arginine Deiminase Methionine Adenosyltransferase (MAT) Sirtuin JAK TET Protein
GPCR/G Protein

5-HT Receptor Adenosine Receptor Adenylate Cyclase (AC) Adrenergic Receptor Angiotensin Receptor Bombesin Receptor Bradykinin Receptor Cannabinoid Receptor CaSR CCR CGRP Receptor Cholecystokinin Receptor CRFR CXCR TSH Receptor Neuropeptide Y Receptor Dopamine Receptor EBI2/GPR183 Endothelin Receptor Formyl peptide receptor (FPR) GHSR Glucagon Receptor GNRH Receptor GPR109A GPR119 GPR139 GPR27 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR MCHR1 (GPR24) Melanocortin Receptor Melatonin Receptor mGluR Motilin Receptor Neurokinin Receptor Neurotensin Receptor Opioid Receptor Orexin Receptor (OX Receptor) Oxytocin Receptor P2Y Receptor PKG Prostaglandin Receptor Protease-Activated Receptor (PAR) Apelin Receptor (APJ) Ras GPR88 Free Fatty Acid Receptor RGS GPR4 Secretin Receptor Mas-related G-protein-coupled Receptor (MRGPR) GPR35 GPR52 MCHR1 (GPR24) Leukotriene Receptor GLP Receptor Somatostatin Receptor Arrestin Platelet-activating Factor Receptor (PAFR) Mas-related G-protein-coupled Receptor (MRGPR) Kisspeptin Receptor G Protein-coupled Receptor Kinase (GRK) G protein-coupled Bile Acid Receptor 1 Succinate Receptor 1 TSH Receptor Protease Activated Receptor (PAR) Urotensin Receptor Vasopressin Receptor Motilin Receptor TF
Immunology/Inflammation

Arginase Aryl Hydrocarbon Receptor (AhR) CCR Complement System COX CXCR Cyclic GMP-AMP Synthase (cGAS) TIM-3 TIGIT CTLA-4 FKBP FLAP Galectin IFNAR Interleukin Related IRAK MIF MyD88 NO Synthase NOD-like Receptor (NLR) PD-1/PD-L1 PGE synthase CX3CR1 Pyroptosis Nuclear Factor of activated T Cells (NFAT) Reactive Oxygen Species AP-1 Salt-inducible Kinase (SIK) SOD SPHK STING Thrombopoietin Receptor Toll-like Receptor (TLR) AP-1 PSMA Glucocorticoid Receptor (GR) FAP Histamine Receptor Macrophage migration inhibitory factor (MIF) LAG-3 Mucin Tim3 Mesothelin Nectin-4 P-selectin TROP2 CD79B DPEP3 BCMA MUC16 BAFF CD markers FcRn CSF2 IgE Glycoprotein VI

Ferroptosis

Ferroptosis 相关靶点

全部(124) Ferroptosis激活剂(56) Ferroptosis抑制剂(50) Ferroptosis诱导剂(10)

货号	产品名	中文名称	产品描述
SJ-MX0556	FIN56		FIN56 是一种特异性的铁死亡 (ferroptosis) 诱导剂。FIN56 通过诱导 Glutathione Peroxidase 4 (GPX4) 降解来诱导铁死亡。FIN56 还结合并激活角鲨烯合酶 (squalene synthase)。
SJ-MX0967B	Pioglitazone (U 72107)	匹格列酮	Pioglitazone (U 72107) 是一种有效的选择性 PPARγ 激动剂，高亲和力结合到 PPARγ 配体结合域。作用于人和鼠 PPARγ，EC50 分别为 0.93 和 0.99 μM。Pioglitazone 可用于糖尿病研究。
SJ-MX0153	ML385		ML385 是一种有效的选择性 Nrf2 抑制剂，IC50 为 1.9 µM。ML-385 阻断 Nrf2 下游靶基因表达，并增强卡铂和其他化疗药物对肺癌细胞 (NSCLC) 的治疗疗效。ML-385 对含有 KEAP1 突变的 NSCLC 细胞 (具有 Nrf2 功能) 具有特异性和选择性。
SJ-MX0373A	Atorvastatin Calcium	阿托伐他汀钙	Atorvastatin Calcium 是一种具有口服活性的、3-羟基-3-甲基戊二酰辅酶 A 还原酶 (HMG-CoA reductase) 抑制剂，可以降低血液中的 LDL (“坏”) 胆固醇和甘油三酯，也可以提高高密度脂蛋白 (“好”) 胆固醇。Atorvastatin Calcium 抑制人 SV-SMC 增殖和侵袭，IC50 分别为 0.39 μM 和 2.39 μM。Atorvastatin Calcium 可诱导凋亡和自噬。