Category: Reagents

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Reference: 29854-5

A synthetic progestogen; prevents the development of osteoporosis in ovariectomized rats at 9 µg/animal per day; inhibits copulatory ovulation in rabbits

Reference: 18662-1

A pyrazine derivative that is used as a flavoring agent in the food and tobacco industry; has DNA strand breakage activity and strongly inhibits IL-2 production by Jurkat cells stimulated with phytohemagglutinin (IC50 = ~1.25 mM)

Reference: B5750-100

serine/threonine kinase STK33 inhibitor

Reference: 29854-500

A synthetic progestogen; prevents the development of osteoporosis in ovariectomized rats at 9 µg/animal per day; inhibits copulatory ovulation in rabbits

Reference: 18662-5

A pyrazine derivative that is used as a flavoring agent in the food and tobacco industry; has DNA strand breakage activity and strongly inhibits IL-2 production by Jurkat cells stimulated with phytohemagglutinin (IC50 = ~1.25 mM)

Reference: B5750-200

serine/threonine kinase STK33 inhibitor

Reference: 29878-1

A synthetic glucocorticoid; selective for the glucocorticoid receptor over the mineralocorticoid, progesterone, and androgen receptors in reporter assays (EC50s = 0.03, 23.4, 0.9, and >10,000 nM, respectively), as well as ERα and ERβ in scintillation proximity assays (EC50s = >10,000 nM); reduces LPS-induced increases in TNF-α production in human PBMCs (EC50 = 0.12 nM); decreases S. aureus enterotoxin-induced increases in IFN-γ, IL-2, IL-5, IL-17, and TNF-α levels in patient-derived nasal polyp tissue in vitro at 100 nM; reduces ovalbumin-induced increases in BALF eosinophil infiltration in a rat model of allergic inflammation at 30 µg/animal intrathecally

Reference: 18662-500

A pyrazine derivative that is used as a flavoring agent in the food and tobacco industry; has DNA strand breakage activity and strongly inhibits IL-2 production by Jurkat cells stimulated with phytohemagglutinin (IC50 = ~1.25 mM)

Reference: B5751-10

partial agonist of hydroxycarboxylic acid receptor 2 (HCA2)

Reference: 29878-10

A synthetic glucocorticoid; selective for the glucocorticoid receptor over the mineralocorticoid, progesterone, and androgen receptors in reporter assays (EC50s = 0.03, 23.4, 0.9, and >10,000 nM, respectively), as well as ERα and ERβ in scintillation proximity assays (EC50s = >10,000 nM); reduces LPS-induced increases in TNF-α production in human PBMCs (EC50 = 0.12 nM); decreases S. aureus enterotoxin-induced increases in IFN-γ, IL-2, IL-5, IL-17, and TNF-α levels in patient-derived nasal polyp tissue in vitro at 100 nM; reduces ovalbumin-induced increases in BALF eosinophil infiltration in a rat model of allergic inflammation at 30 µg/animal intrathecally

Reference: 18673-1

A chemiluminescent probe for superoxide production by activated leukocytes

Reference: B5751-50

partial agonist of hydroxycarboxylic acid receptor 2 (HCA2)