Netoglitazone

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) is a potent, selective and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. (-)-DHMEQ inhibits nuclear translocation of NF-κB and shows anti-inflammatory and anticancer activityIn

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) is a potent, selective and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. (-)-DHMEQ inhibits nuclear translocation of NF-κB and shows anti-inflammatory and anticancer activityIn

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) is a potent, selective and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. (-)-DHMEQ inhibits nuclear translocation of NF-κB and shows anti-inflammatory and anticancer activityIn

(-)-DHMEQ (Dehydroxymethylepoxyquinomicin) is a potent, selective and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. (-)-DHMEQ inhibits nuclear translocation of NF-κB and shows anti-inflammatory and anticancer activityIn

Product Application：1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester can be used as a reactant:In Suzuki coupling reaction for the preparation of heteroaryl scaffolds via formation of C-C bond.To synthesize darolutamide

Product Application：1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester can be used as a reactant:In Suzuki coupling reaction for the preparation of heteroaryl scaffolds via formation of C-C bond.To synthesize darolutamide

Product Application：1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester can be used as a reactant:In Suzuki coupling reaction for the preparation of heteroaryl scaffolds via formation of C-C bond.To synthesize darolutamide

Product Application：1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester can be used as a reactant:In Suzuki coupling reaction for the preparation of heteroaryl scaffolds via formation of C-C bond.To synthesize darolutamide

One of the five primary enzymatic prostaglandins derived directly from PGH2. Many of the biological effects of PGD2 are transduced in vivo by a classical 7-transmembrane GPCR, the DP1 receptor. However, a second receptor, the chemokine-related CRTH2

One of the five primary enzymatic prostaglandins derived directly from PGH2. Many of the biological effects of PGD2 are transduced in vivo by a classical 7-transmembrane GPCR, the DP1 receptor. However, a second receptor, the chemokine-related CRTH2

An amide of docosenoic acid first identified in the CSF of sleep-deprived cats causes reduced mobility and slightly lessened awareness in rats.

15(R)-PGF2&alpha is the C-15 epimer of the naturally occurring mammalian autacoid PGF2&alpha. It has only 25% of the potency of PGF2&alpha in hamster antifertility studies, which may be due to reduced affinity for FP receptors.