Search results for 'ganoderic acid'
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PF 750
PF 750 is an irreversible fatty acid amide hydrolase (FAAH) inhibitor that displays no activity at a range of other serine hydrolases. Learn MoreStarting at: $149.00
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SA 47
SA 47 is a selective inhibitor of fatty acid amide hydrolase (FAAH) that exhibits greater selectivity for FAAH than URB 597 against multiple carboxylesterases. Learn MoreStarting at: $109.00
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Trequinsin hydrochloride
Trequinsin hydrochloride is an extremely potent inhibitor of cGMP-inhibited phosphodiesterase that inhibits arachidonic acid-induced aggregation of human platelets. Learn MoreStarting at: $199.00
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SKF 86002 dihydrochloride
SKF 86002 dihydrochloride is an inhibitor of p38 MAP kinase that potently inhibits LPS-induced IL-1 and TNF-α production in human monocytes (IC50 = 1 μM) and also inhibits 5-lipoxygenase- and cyclooxygenase-mediated arachidonic acid metabolism in RBL-1 cells. Learn MoreStarting at: $149.00
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URB 597
URB 597, a potent and selective fatty acid amide hydrolase (FAAH) inhibitor, displays antiallodynic and antihyperalgesic activity in an inflammatory pain model. Learn MoreStarting at: $98.00
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C 75
C 75 is a synthetic inhibitor of fatty acid synthase (FAS) which inhibits fatty acid synthesis in vitro and in vivo and displays anorectic effects. Induces apoptosis in MCF-7 xenografts and exhibits anti-tumor activity. Learn MoreStarting at: $135.00
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AACOCF3
AACOCF3 is an inhibitor of cytosolic (85 kDa) phospholipase A2. It also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Learn MoreStarting at: $65.00
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WIN 18446
WIN 18446 is an inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2) (IC50 = 0.3 μM) which inhibits the biosynthesis of retinoic acid from retinol in neonatal and adult murine testis. Learn MoreStarting at: $80.00
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SA 57
SA 57 is a potent inhibitor of fatty acid amide hydrolase (FAAH) (IC50 < 10 nM), which inhibits both human and mouse FAAH enzymes and displays inhibitory activity against FAAH, MAGL and ABHD6 in vivo. Learn MoreStarting at: $100.00
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TC-F 2
TC-F 2 is a potent, reversible inhibitor of fatty acid amide hydrolase (FAAH) (IC50 values are 28 and 100 nM for human and rat FAAH respectively), which displays selectivity for FAAH over cannabinoid-related targets (IC50 > 20 μM for CB1, CB2 and TRPV1). Learn MoreStarting at: $155.00
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(-)-Terreic acid
Selective inhibitor of Bruton's tyrosine kinase (BTK), which inhibits the interaction between PKCbII and BTK (IC50 ~ 30 mM) and the catalytic activity of BTK but does not affect the activity of PKC. Learn MoreStarting at: $155.00