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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16280 |
Nedocromil
FPL 59002,尼多克罗 |
Leukotriene Receptor; Prostaglandin Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Nedocromil (FPL 59002) 对多种介质的作用或形成有抑制作用,包括组胺,前列腺素 D2和白三烯 C4。 | |||
T1677L |
Montelukast sodium
MK0476,孟鲁司特钠 |
Leukotriene Receptor; LTR | GPCR/G Protein; Immunology/Inflammation |
Montelukast sodium (MK0476) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 | |||
T1677 |
Montelukast
孟鲁司特,Singular |
Leukotriene Receptor; Lipoxygenase; LTR | GPCR/G Protein; Immunology/Inflammation; Metabolism |
Montelukast (Singular) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 | |||
T22946 |
LY255283
LY 255283 |
Leukotriene Receptor | GPCR/G Protein |
LY255283 是白三烯 B4 (LTB4) 受体的特异性拮抗剂,抑制人外周血多形核白细胞和由钙离子载体 A23187 激活的单核细胞中 LTB(4) 的产生。 | |||
T26519 |
Ablukast
Ro 23-3544,阿鲁司特 |
Leukotriene Receptor | GPCR/G Protein |
Ablukast (Ro 23-3544) 是白三烯受体的选择性拮抗剂,也是LTD4受体拮抗剂。可改善 LTC4 和抗原诱导的支气管狭窄。 | |||
T6893 |
MK-886
MK886,L 663536 |
Apoptosis; Leukotriene Receptor; COX; PPAR; FLAP | Apoptosis; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
MK-886 (L 663536)是一种细胞可渗透的,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。它也是一种非竞争性PPARα拮抗剂,可以诱导细胞凋亡。 | |||
T0694 |
Pranlukast
普鲁司特,ONO-1078,普仑司特 |
Leukotriene Receptor; IL Receptor; Others; TNF; NF-κB; LTR | Apoptosis; GPCR/G Protein; Immunology/Inflammation; NF-κB; Others |
Pranlukast (ONO-1078) 是一种半胱氨酰白三烯受体 1 拮抗剂,可拮抗或减少支气管痉挛,用于哮喘研究。 | |||
T20615 |
Olsalazine
奥沙拉嗪,Dipentium,Salicylic acid |
Others | Others |
Olsalazine (Dipentium) 是一种抗炎药,用于治疗炎症性肠病。它也是一种新型的 DNA 去甲基化剂。 | |||
T6736 |
Zafirlukast
Vanticon,ICI 204219,Accolate,扎鲁司特 |
Leukotriene Receptor | GPCR/G Protein |
Zafirlukast (ICI 204219) 是一种可口服的白三烯 D4受体拮抗剂,具有平喘、抗炎和抗菌作用。 | |||
T22358 |
Etalocib
LY293111,VML295 |
Apoptosis; Leukotriene Receptor; LTR | Apoptosis; GPCR/G Protein; Immunology/Inflammation |
Etalocib (LY293111) 是一种具有口服活性的白三烯(LTB4)受体的拮抗剂,抑制 [3H]LTB4结合的 Ki 值为 25 nM。它还可诱导凋亡。它抑制 LTB4诱导的钙动员,lC50值为 20 nM。 | |||
T3148 |
MK-571 sodium
L-660711 (sodium salt),L-660711 sodium salt,Verlukast sodium,L-660711,MK571,MK-571 sodium salt,Propanoic acid |
Leukotriene Receptor; LTR | GPCR/G Protein; Immunology/Inflammation |
MK-571 sodium (L-660711 sodium salt) 是一种可口服的选择性白三烯 D4受体拮抗剂,在豚鼠和人肺膜的 Ki 分别为0.22 和 2.1 nM。 | |||
T15002 |
CP-105696
Pfizer 105696 |
LTR | Immunology/Inflammation |
CP-105696 是一种具有强效性和选择性白三烯 B4 (LTB4) 受体拮抗剂,可用于研究异体移植物排斥反应。 | |||
T27979 |
Masilukast
ICI-D-3523,ZD-3523,ICI D-3523,MCC-847,SA-09012,D-3523 |
Leukotriene Receptor | GPCR/G Protein |
Masilukast(MCC-847) 是一种口服的白三烯D4 (LTD4) 受体拮抗剂,可用于研究与炎症相关的疾病。 | |||
T22787 |
FPL 55712
|
LTR | Immunology/Inflammation |
FPL 55712 是白三烯受体和 SRS-A 拮抗剂,抑制支气管收缩,可用于研究哮喘和冠状动脉血栓。 | |||
T68130 |
Pobilukast
SKF 104353 Z2,SKF 104353 |
Leukotriene Receptor | GPCR/G Protein |
Pobilukast (SKF 104353) 是一种选择性半胱氨酰白三烯受体拮抗剂,可阻断磷脂酰肌醇代谢和白三烯D诱导的血栓素合成,可用于研究过度心肌再灌注损伤 (MI/R) 大鼠限制心肌损伤。 | |||
T21821L |
REV 5901A
REV 5901 HCl,REV 5901A(101910-24-1 Free base) |
Leukotriene Receptor; Lipoxygenase; Antibiotic | GPCR/G Protein; Metabolism; Microbiology/Virology |
REV 5901A (REV 5901 HCl) 是一种具有口服活性的白三烯受体 (leukotriene receptor) 拮抗剂,也是一种 5-脂氧合酶 (5-lipoxygenase) 抑制剂,具有抗菌活性,可减弱小鼠体内结肠癌的生长。REV 5901A 可用于研究哮喘和心肌梗死。 | |||
T68119 |
Ontazolast
BIRM-270 |
LTR | Immunology/Inflammation |
Ontazolast 是一种小分子白三烯B4受体(LTB4R)拮抗剂,可用于治疗免疫系统疾病和呼吸系统疾病。Ontazolast 是治疗哮喘的候选化合物。 | |||
T68108L |
Moxilubant HCl
Moxilubant hcl(146978-48-5 Free base) |
LTR | Immunology/Inflammation |
Moxilubant HCl 是一种小分子白三烯 B4 受体 1(LTB4R)拮抗剂,可用于治疗免疫系统疾病、皮肤和肌肉骨骼疾病,可用于研究银屑病和类风湿关节炎。 | |||
T28974 |
Ticolubant
|
Calcium Channel; LTR | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Ticolubant 是一种具有口服活性的白三烯 B4 拮抗剂,对人类中性粒细胞 LTB4 受体具有很高的亲和力(Ki = 0.78 nM),能阻断 LTB4 诱导的 Ca2+ 迁移,IC50 为 6.6±1.5 nM,并在小鼠皮肤炎症模型中显示出局部抗炎活性。 | |||
T4657 |
WHI-P97
4-(3',5'-二溴-4-羟基苯基)氨基-6,7-二甲氧基喹唑啉 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
WHI-P97 是一种选择性 JAK-3抑制剂,可用于预防过敏性哮喘的研究。 | |||
T22668 |
Cinalukast
|
Others | Others |
CysLT1 leukotriene receptor antagonist | |||
T27893 |
LY 203647
LY203647,LY-203647 |
Others | Others |
LY 203647 is a antagonist of leukotriene D4 and E4 receptor. | |||
T27916 |
LY 306669
LY-306669,LY306669 |
Others | Others |
LY 306669 is an antagonist of leukotriene B4 receptor. | |||
T24304 |
L 648051
4-Apsob,L48051,L-648051 |
Others | Others |
L 648051 is a leukotriene D4 receptor antagonist. | |||
T27896 |
LY 213024
LY-213024,LY213024 |
Others | Others |
LY 213024 is an antagonist of leukotriene B4 receptor. | |||
T27912 |
LY 290324
LY-290324,LY290324 |
Others | Others |
LY 290324 is an orally active, potent and selective antagonist of cysteinyl leukotriene (LTD4) receptor. | |||
T69278 |
FPL-55712
|
Others | Others |
FPL-55712 is a CysLT1 leukotriene receptor antagonist. | |||
T28699 |
SC-41930
CGS 24115,SC41930,CGS24115 |
Others | Others |
SC-41930 is a potent and selective antagonist of leukotriene B4 receptor. | |||
T30827 |
Cgp 33304
Cgp-33304,Cgp33304 |
Others | Others |
CGP 33304 is a dual leukotriene receptor antagonist and phospholipase A2 inhibitor. It prevents hypoxia secondary to bronchial constriction induced by leukotriene in a shocking state. | |||
T27913 |
LY 292728
LY292728,LY-292728 |
Others | Others |
LY 292728 is a highly potent antagonist of leukotriene B4 receptor. | |||
T28527 |
RG 14893
|
Others | Others |
RG 14893 is a antagonist of high-affinity leukotriene B4 receptor. | |||
T71043 |
MDL-43291
|
Others | Others |
MDL-43291 is a leukotriene receptor antagonist. | |||
T15801 |
LY210073
|
Others | Others |
LY210073 is an antagonist of the Leukotriene B4 (LTB4) receptor (IC50: 6.2 nM). | |||
T26809 |
BIIL 260
BIIL260,BIIL-260 |
Others | Others |
BIIL 260 is a leukotriene B4 (BLT1) receptor antagonist with anti-inflammatory activity. | |||
T15803 |
LY223982
SKF107324,CGS23131 |
Others | Others |
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor. | |||
T70477 |
SC 53228
|
Others | Others |
SC 53228 is a specific leukotriene B4 receptor antagonist. | |||
T68418 |
Furodysinin lactone
|
Others | Others |
Furodysinin lactone is an agonist of human leukotriene B4 receptor. | |||
T11764 |
KP496
|
Others | Others |
KP496 is a selective, dual antagonist for Thromboxane A2 receptor and Leukotriene D4 receptor. | |||
T68831 |
Furodysinin
|
Others | Others |
Furodysinin is an agonist of human leukotriene B4 receptor. | |||
T10873 |
CP-96486
|
Others | Others |
CP-96486 is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor (Kis: 20 and 24 nM). | |||
T68348 |
Montelukast methylstyrene
|
Others | Others |
Montelukast methylstyrene is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. | |||
T73793 |
20-Carboxy-Leukotriene B4
|
Others | Others |
20-Carboxy-Leukotriene B4 (20-COOH LTB4) 是 Leukotriene B4 (LTB4) 的代谢物。20-Carboxy-Leukotriene B4 以高亲和力与 BLT1 受体结合。20-Carboxy-Leukotriene B4 抑制 LTB4 介导的中性粒细胞反应,迁移、脱粒、白三烯生物合成。 | |||
T71152 |
Montelukast bis-sulfide
|
Others | Others |
Montelukast bis-sulfide is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. | |||
T68496 |
Montelukast cyclopropaneacetamide
|
Others | Others |
Montelukast cyclopropaneacetamide is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. | |||
T10872 |
CP-96021 hydrochloride
|
Others | Others |
CP-96021 hydrochloride is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor receptor (Kis: 34 nM and 37 nM). | |||
T68295 |
Montelukast methyl ketone
|
Others | Others |
Montelukast methyl ketone is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. | |||
T21821 |
REV 5901
|
Others | Others |
REV 5901 是一种口服有效的白三烯受体 (leukotriene receptor) 竞争性拮抗剂,Ki 值为 0.7 μM。REV 5901 也是一种 5-脂氧合酶 (5-lipoxygenase) 抑制剂。REV 5901 可用于涉及白三烯释放的哮喘研究。 | |||
T27815 |
Leucettamol A
Leucettamine A |
Others | Others |
Leucettamol A is a leukotriene B4 receptor antagonist isolated from the marine sponge Leucetta microraphis. It inhibits the formation of a complex composed of the ubiquitin E2 enzyme Ubc13 and Uev1A. | |||
T71369 |
Montelukast sulfoxide
|
Others | Others |
Montelukast sulfoxide is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. | |||
T69501 |
Montelukast alcohol
|
Others | Others |
Montelukast alcohol is a leukotriene receptor antagonist (LTRA) used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7786 |
Tryptanthrin
|
DNA gyrase | DNA Damage/DNA Repair |
Tryptanthrin 是一种口服具有活性的细胞内Leukotriene (LT) biosynthesis 抑制剂。 它能够降低大鼠胸膜炎模型中的 LTB4 水平,并抑制人全血中Leukotriene 的形成 (IC50= 10 µM)。 | |||
T5714 |
5-O-Demethylnobiletin
5-DEMETHYLNOBILETIN,去甲基川陈皮素 |
Leukotriene Receptor; Lipoxygenase | GPCR/G Protein; Metabolism |
5-O-Demethylnobiletin (5-DEMETHYLNOBILETIN) 是从黄芪中分离出的多甲氧基黄酮,具有抗炎活性,可通过直接抑制 5-LOX 发挥作用,IC50为 0.1 μM。 | |||
TN1182 |
11-Keto-beta-boswellic acid
11-Keto-beta-boswellic acid,11-酮基-BETA-乳香酸 |
Leukotriene Receptor; NF-κB; Lipoxygenase | GPCR/G Protein; Metabolism; NF-κB |
11-Keto-beta-boswellic acid 是来自乳香的一种五环三萜酸,具有抗炎活性和剂量依赖性心脏保护作用,主要是由于抑制5-脂氧合酶、白三烯、NF-κB 的激活和肿瘤坏死因子 α 的产生。 | |||
T21504 |
γ-Linolenic Acid methyl ester
Methyl gamma-linolenate,γ-亚麻酸甲酯 |
LTR | Immunology/Inflammation |
γ-Linolenic Acid methyl ester (Methyl gamma-linolenate) 是一种弱白三烯 B4 (LTB4) 受体拮抗剂。 | |||
T4973 |
Paraxanthine
1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE |
Endogenous Metabolite | Metabolism |
Paraxanthine (1,7-dimethylxanthine) 是一种 caffeine 的代谢物,能够刺激Ryanodine 受体通道来抑制多巴胺能细胞的死亡。 | |||
T37972 |
12-OxoETE
|
Others | Others |
12-OxoETE is synthesized by human platelets and Aplysia nervous tissue after incubation with arachidonic acid. Microsomal fractions of various tissues will reduce 12-oxoETE to 12(S)-HETE or a mixture of 12(S)- and 12(R)-HETE. 12-OxoETE induces a rapid, dose dependent increase of cytoplasmic free calcium via a leukotriene B4 receptor or a common activation sequence. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-03749 |
CYSLTR1 Protein, Human, Recombinant (His)
Cysteinyl leukotriene receptor 1,G-protein... |
Human | E. coli |
Receptor for cysteinyl leukotrienes mediating bronchoconstriction of individuals with and without asthma. Stimulation by LTD4 results in the contraction and proliferation of smooth muscle, edema, eosinophil migration and damage to the mucus layer in the lung. This response is mediated via a G-protein that activates a phosphatidylinositol-calcium second messenger system. The rank order of affinities for the leukotrienes is LTD4 >> LTE4 = LTC4 >> LTB4. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0609 |
Zafirlukast-d7
|
||
Zafirlukast-d7 是 Zafirlukast 的氘代化合物。Zafirlukast 的 CAS 号为 107753-78-6。Zafirlukast 是一种可口服的白三烯 D4受体拮抗剂,具有平喘、抗炎和抗菌作用。 | |||
TMIJ-0329 |
Montelukast-d6
|
||
Montelukast-d6 是 Montelukast 的氘代化合物。Montelukast 的 CAS 号为 158966-92-8。Montelukast 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 |