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![8-[[(3r,4r)-3-[(1,1-dioxothian-4-yl)methoxy]piperidin-4-yl]amino]-3-methyl-1h-1,7-naphthyridin-2-one (c09-1166-485)](https://cdn11.bigcommerce.com/s-2u2oi3cvy8/images/stencil/500x659/products/1630770/1462025/sj_500_R609119__24422.1721230457.jpg?c=1 "8-[[(3r,4r)-3-[(1,1-dioxothian-4-yl)methoxy]piperidin-4-yl]amino]-3-methyl-1h-1,7-naphthyridin-2-one (c09-1166-485)")
Add to Cart The item has been addedR609119-5mgAladdin
8-[[(3R,4R)-3-[(1,1-dioxothian-4-yl)methoxy]piperidin-4-yl]amino]-3-methyl-1H-1,7-naphthyridin-2-one (C09-1166-485)
Price: $734.01List Price: $815.578-[[(3R,4R)-3-[(1,1-dioxothian-4-yl)methoxy]piperidin-4-yl]amino]-3-methyl-1H-1,7-naphthyridin-2-one -
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Add to Cart The item has been addedI392115-100μgIts been reported that anandamide (AEA) can be used directly by cyclooxygenase-2 and specific prostaglandin H2 (PGH2) isomerases to produce ethanolamide congeners of the classical PGs, including PGF2α.(1) PGF2α. Ethanolamide has also been reported -
Add to Cart The item has been addedI392115-1mgIts been reported that anandamide (AEA) can be used directly by cyclooxygenase-2 and specific prostaglandin H2 (PGH2) isomerases to produce ethanolamide congeners of the classical PGs, including PGF2α.(1) PGF2α. Ethanolamide has also been reported -
Add to Cart The item has been addedI392115-500μgIts been reported that anandamide (AEA) can be used directly by cyclooxygenase-2 and specific prostaglandin H2 (PGH2) isomerases to produce ethanolamide congeners of the classical PGs, including PGF2α.(1) PGF2α. Ethanolamide has also been reported -
Add to Cart The item has been addedO425963-1mlInformation8-OH-DPAT (8-Hydroxy-DPAT) is a kind of classic5-HT1Aagonist with the pIC50 of 8.19. It has a selectivity of almost-1000 fold for a subtype of the 5-HT1 binding site Its biological half-life is 1.5 hous.Targets5-HT1A (Cell-free) -
Add to Cart The item has been addedO414014-100mgInformation8-OH-DPAT (8-Hydroxy-DPAT) is a kind of classic5-HT1Aagonist with the pIC50 of 8.19. It has a selectivity of almost-1000 fold for a subtype of the 5-HT1 binding site Its biological half-life is 1.5 hous.Targets5-HT1A (Cell-free) -
Add to Cart The item has been addedO414014-10mgInformation8-OH-DPAT (8-Hydroxy-DPAT) is a kind of classic5-HT1Aagonist with the pIC50 of 8.19. It has a selectivity of almost-1000 fold for a subtype of the 5-HT1 binding site Its biological half-life is 1.5 hous.Targets5-HT1A (Cell-free) -
Add to Cart The item has been addedO414014-25mgInformation8-OH-DPAT (8-Hydroxy-DPAT) is a kind of classic5-HT1Aagonist with the pIC50 of 8.19. It has a selectivity of almost-1000 fold for a subtype of the 5-HT1 binding site Its biological half-life is 1.5 hous.Targets5-HT1A (Cell-free)
