Category: Reagents

Active filters

Reference: 29590-10

An SPM; produced from EPA by 15-LO via 15(S)-HpEPE and 15S-hydroxy, 5S-HpEPE intermediates in vitro and by isolated human M2 macrophages or PMN neutrophils under normoxic or hypoxic conditions; enhanced synthesis in M2 macrophage and neutrophil co-cultures, indicating transcellular biosynthesis by a potential 15-LO and 5-LO mechanism; has been found in mouse inflammatory exudates; increases efferocytosis of apoptotic neutrophils or sRBCs by human M2 macrophages under hypoxic conditions in vitro; inhibits zymosan A- and thrombin-induced increases in inflammatory exudate neutrophil infiltration in a mouse model of hemorrhagic peritonitis at 100 ng/animal; increases inflammatory exudate macrophage infiltration and efferocytosis of apoptotic neutrophils and/or RBCs in the same model

Reference: 18657-10

An antagonist of sweet taste receptors that blocks the activation of T1R3 by natural and synthetic sweeteners and increases the inhibition of T1R2 by umami compounds; used to explore the roles of these receptors in diverse pathways

Reference: B5747-5

calcium-activated chloride channel (CaCC) inhibitor

Reference: 29590-100

An SPM; produced from EPA by 15-LO via 15(S)-HpEPE and 15S-hydroxy, 5S-HpEPE intermediates in vitro and by isolated human M2 macrophages or PMN neutrophils under normoxic or hypoxic conditions; enhanced synthesis in M2 macrophage and neutrophil co-cultures, indicating transcellular biosynthesis by a potential 15-LO and 5-LO mechanism; has been found in mouse inflammatory exudates; increases efferocytosis of apoptotic neutrophils or sRBCs by human M2 macrophages under hypoxic conditions in vitro; inhibits zymosan A- and thrombin-induced increases in inflammatory exudate neutrophil infiltration in a mouse model of hemorrhagic peritonitis at 100 ng/animal; increases inflammatory exudate macrophage infiltration and efferocytosis of apoptotic neutrophils and/or RBCs in the same model

Reference: 18657-25

An antagonist of sweet taste receptors that blocks the activation of T1R3 by natural and synthetic sweeteners and increases the inhibition of T1R2 by umami compounds; used to explore the roles of these receptors in diverse pathways

Reference: B5747-10

calcium-activated chloride channel (CaCC) inhibitor

Reference: 29590-25

An SPM; produced from EPA by 15-LO via 15(S)-HpEPE and 15S-hydroxy, 5S-HpEPE intermediates in vitro and by isolated human M2 macrophages or PMN neutrophils under normoxic or hypoxic conditions; enhanced synthesis in M2 macrophage and neutrophil co-cultures, indicating transcellular biosynthesis by a potential 15-LO and 5-LO mechanism; has been found in mouse inflammatory exudates; increases efferocytosis of apoptotic neutrophils or sRBCs by human M2 macrophages under hypoxic conditions in vitro; inhibits zymosan A- and thrombin-induced increases in inflammatory exudate neutrophil infiltration in a mouse model of hemorrhagic peritonitis at 100 ng/animal; increases inflammatory exudate macrophage infiltration and efferocytosis of apoptotic neutrophils and/or RBCs in the same model

Reference: 18657-5

An antagonist of sweet taste receptors that blocks the activation of T1R3 by natural and synthetic sweeteners and increases the inhibition of T1R2 by umami compounds; used to explore the roles of these receptors in diverse pathways

Reference: B5747-25

calcium-activated chloride channel (CaCC) inhibitor

Reference: 29590-50

An SPM; produced from EPA by 15-LO via 15(S)-HpEPE and 15S-hydroxy, 5S-HpEPE intermediates in vitro and by isolated human M2 macrophages or PMN neutrophils under normoxic or hypoxic conditions; enhanced synthesis in M2 macrophage and neutrophil co-cultures, indicating transcellular biosynthesis by a potential 15-LO and 5-LO mechanism; has been found in mouse inflammatory exudates; increases efferocytosis of apoptotic neutrophils or sRBCs by human M2 macrophages under hypoxic conditions in vitro; inhibits zymosan A- and thrombin-induced increases in inflammatory exudate neutrophil infiltration in a mouse model of hemorrhagic peritonitis at 100 ng/animal; increases inflammatory exudate macrophage infiltration and efferocytosis of apoptotic neutrophils and/or RBCs in the same model

Reference: 18657-50

An antagonist of sweet taste receptors that blocks the activation of T1R3 by natural and synthetic sweeteners and increases the inhibition of T1R2 by umami compounds; used to explore the roles of these receptors in diverse pathways

Reference: B5747-50

calcium-activated chloride channel (CaCC) inhibitor