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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
Apoptosis

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

Autophagy FKBP LRRK2 Mitophagy OGA ULK
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 HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 DNA Stain Nucleoside Antimetabolite/Analog Nur77 p97 PAK PARP PERK Polo-like Kinase (PLK) PPAR RAD51 Cyclin G-associated Kinase (GAK) Nucleoside Antimetabolite/AnalogOrthopoxvirus ROCK ATF6 Haspin Kinase Sirtuin SRPK Telomerase TOPK Topoisomerase Wee1
Cytoskeletal Signaling

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

Adrenergic Receptor Androgen Receptor Angiotensin-converting Enzyme (ACE) Aromatase Cholecystokinin Receptor TSH Receptor Estrogen Receptor/ERR GHSR Glucocorticoid Receptor GNRH Receptor Mineralocorticoid Receptor Opioid Receptor PGD synthase PGE synthase Progesterone Receptor Thyroid Hormone Receptor
Epigenetics

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

5-HT Receptor Adenosine Receptor Adenylate Cyclase (AC) Adiponectin Receptor 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 Glucocorticoid Receptor GNRH Receptor GPCR19 GPR109A GPR119 GPR120 GPR139 GPR27 GPR40 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR Melanocortin Receptor Melatonin Receptor mGluR 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 E3 Ligase Ligand-Linker Conjugates RGS GPR4 Secretin Receptor Mas-related G-protein-coupled Receptor (MRGPR) GPR35 GPR52 MCHR1 (GPR24) Leukotriene Receptor GLP Receptor Somatostatin Receptor Vasopressin Receptor

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Leukotriene Receptor

Leukotriene Receptor相关产品（11）

货号	产品名	中文名称	产品描述
SJ-MX2133A	Montelukast sodium	孟鲁司特钠	Montelukast sodium is a brain-penetrant cysteinyl leukotriene 1 (CysLT1) receptor antagonist (IC50 = 4.9 nM in HEK293 cell membranes expressing the human receptor). It is selective for CysLT1 over CysLT2 receptors (IC50 = >10,000 nM in COS-7 cell membranes expressing the human receptor). Reduces neuroinflammation, improves blood brain barrier (BBB) integrity, enhances learning and memory, and restores hippocampal neurogenesis and cognitive function in aged rats.
SJ-MN1557	5-O-Demethylnobiletin	去甲基川陈皮素	5-O-Demethylnobiletin (5-Demethylnobiletin) 5-O-去甲肾上腺素，一种从黄芪中分离出的多甲氧基黄酮，是 5-LOX 的直接抑制剂 (IC50=0.1 mM)，不影响 COX-2 的表达。5-O-Demethylnobiletin (5-Demethylnobiletin) 5-O-去甲肾上腺素具有抗炎活性，抑制大鼠中性粒细胞中白三烯 B (4)(LTB4) 的形成和人嗜中性粒细胞中弹性蛋白酶的释放，IC50 值为0.35 mM.
SJ-MX1755	MK-886 (L 663536)		MK-886 (L 663536) 是一种有效的，细胞可渗透的且具有口服活性的 FLAP (IC50 为 30 nM) 和白三烯生物合成 (完整白细胞和人全血中的 IC50 分别为 3 nM 和 1.1μM) 的抑制剂。MK-886 也是一种非竞争性 PPARα拮抗剂，可以诱导细胞凋亡。
SJ-MX2132	Zafirlukast	扎鲁司特	Zafirlukast 是一种有效的具有口服活性的白三烯 D4 (LTD4) 受体拮抗剂。Zafirlukast 具有平喘、抗炎和抗菌作用。
SJ-MX2133	Montelukast	孟鲁司特	Montelukast 是一种有效的、选择性和具有口服活性的半胱氨酸白三烯受体 1 (CysLT1) 拮抗剂。Montelukast 可用于研究预防哮喘和肝损伤。Montelukast 在肠缺血-再灌注损伤中也具有抗氧化作用，还可以减少心脏损伤。Montelukast 减少嗜酸性粒细胞浸润到哮喘气道。
SJ-MX3844	Tryptanthrin		Tryptanthrin 是一种产自靛蓝植物的生物碱。Tryptanthrin 是一种口服有效的细胞白三烯 ( Leukotriene，LT) 生物合成抑制剂。 Tryptanthrin 抑制人全血中Leukotriene 的形成 (IC50 = 10 µM)，并降低大鼠胸膜炎模型中的 LTB4 水平。Tryptanthrin 具有抗癌活性。Tryptanthrin 可抑制 NOS1、COX-2、NF-κB 的表达水平，调节 IL-2、IL-10、TNF-α 的表达水平。
SJ-MX2867	MK-571 sodium		MK-571 sodium 是多药耐药蛋白-1（MRP1）抑制剂 MK-571 的钠盐。MK-571是CysLT1受体的选择性口服活性拮抗剂。
SJ-MX2694	Pranlukast	普鲁司特	Pranlukast 是一种有效的、竞争性的、选择性的半胱氨酸白三烯受体-1 (CysLT1) 拮抗剂。Pranlukast 抑制 [³H]LTE4，[³H]LTD4 和 [³H]LTC4 与肺膜结合，Ki 分别为 0.63±0.11，0.99±0.19 和 5640±680 nM。Pranlukast 诱导支气管收缩，增加微血管通透性，是冠状动脉血管收缩剂。
SJ-MX4895	Etalocib
SJ-MX5468	LY255283
SJ-MX5793	Leukotriene B4