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Cat. No.	Product Name	Target	Signaling Pathways
T72625	LTB4 antagonist 1	Leukotriene Receptor	GPCR/G Protein
	LTB4 antagonist 1为甲酰胺化合物，高效拮抗白三烯B4 (LTB4)，IC50值为288 nM，呈现出明显的抗炎活性。
T78677	LTB4 antagonist 2	Leukotriene Receptor	GPCR/G Protein
	LTB4 antagonist 2为甲酰胺化合物，白三烯B4 (LTB4) 拮抗剂，显示抗炎潜能。该化合物对LTB4受体亲和力高，IC50值为439 nM。
T38157	Ricinelaidic Acid
	Ricinelaidic acid is a 12-hydroxy fatty acid and an antagonist of leukotriene B4 (LTB4) receptors (Ki = 2 μM in porcine neutrophil membranes). It inhibits chemotaxis and calcium flux induced by LTB4 in isolated human neutrophils (IC50s = 10 and 7 μM, respectively). Ricinelaidic acid (1 mg/kg, i.v.) inhibits bronchoconstriction induced by LTB4 in rats by 46%.
T78678	LTB4 antagonist 3	Leukotriene Receptor	GPCR/G Protein
	LTB4 antagonist 3 (compound 24e)为一种具有抗炎活性的LTB4拮抗剂，其IC50为477 nM。
T37260	14,15-dehydro Leukotriene B4 14,15-dehydro Leukotriene B4
	Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-lipoxygenase pathway. It promotes a number of leukocyte functions including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis. At least two LTB4 receptors, termed BLT1 and BLT2, have been identified. 14,15-dehydro LTB4 is a LTB4 receptor antagonist that has a higher binding affinity for BLT1, demonstrating a Ki value ...
T14210	Amelubant BIIL 284	LTR	Immunology/Inflammation
	Amelubant (BIIL 284) is a prodrug of active metabolites BIIL 260 and BIIL 315. Anti-inflammatory activity[1]. Amelubant (BIIL 284) is a potent, oral and long acting LTB4 receptor antagonist, negligibly binds to LTB4 receptor, with Kis of 221 nM and 230 nM
T79418	BLT2 antagonist-1	Leukotriene Receptor	GPCR/G Protein
	BLT2 agonist-1 (compound 15b) 是选择性BLT2拮抗剂，能在224 nM IC50下抑制CHO-BLT2细胞趋化性。它不影响CHO-BLT1细胞趋化性，并在132 nM Ki值下抑制LTB4与BLT2结合。BLT2 agonist-1适用于哮喘、慢性阻塞性肺病等炎症性气道疾病研究。
T41235	γ-Linolenic acid ethyl ester
	γ-Linolenic acid ethyl ester (Ethyl γ-linolenate) 是一种白三烯 B 受体 4(LTB4)的拮抗剂，具有潜在的抗炎作用。