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Supplier: Thermo Fisher Scientific
Description: 2-Nitrobenzamide 98
Supplier: ENZO LIFE SCIENCES
Description: AACOCF3 is a trifluoromethylketone derivative of arachidonic acid. It is a selective inhibitor of human cytosolic PLA2 and Ca2+-independent PLA2 (iPLA2, IC50=15 µM). It is active in intact platelets and U937 cells (IC50=8 µM). It also inhibits fatty acid amide hydrolase (100% at 7.5 µM).

New Product

Catalog Number: (ENZOBMLKI2830500)
Supplier: ENZO LIFE SCIENCES
Description: Nicotinamide, the water-soluble amide of nicotinic acid, is a component of the two most important coenzymes-nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate. Nicotinamide is involved in numerous oxidation-reduction reactions in mammalian biological systems acting as an antioxidant.
UOM: 1 * 500 µl

New Product


Supplier: Cayman Chemical
Description: A sensitive detection method for measuring both the free acid and ethyl amide forms of 17-phenyl trinor PGF<sub>2α</sub>.

Supplier: Thermo Fisher Scientific
Description: Benzamide 98
Supplier: Thermo Fisher Scientific
Description: 4-Methoxybenzamide 97%
Supplier: Apollo Scientific
Description: Anthranilamide

Supplier: Apollo Scientific
Description: 4-Ethoxybenzamide 95%

Catalog Number: (APOSOR925166-25G)
Supplier: Apollo Scientific
Description: 3-Methoxybenzamide 95%
UOM: 1 * 25 g


Supplier: Apollo Scientific
Description: Derivatised D- and L- amino acids can be resolved and quantified by HPLC. For reference see:Marfey, P. (1984) Carlsberg Res. Commun. 49, 591
Catalog Number: (BOSSBS-11102R)
Supplier: Bioss
Description: Metalloprotease involved in sperm function, possibly by modulating the processes of fertilization and early embryonic development. Degrades a broad variety of small peptides with a preference for peptides shorter than 3 kDa containing neutral bulky aliphatic or aromatic amino acid residues. Shares the same substrate specificity with MME and cleaves peptides at the same amide bond (By similarity).
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: Appearance: White to off-white Powder
Catalog Number: (ENZOBPDABS029011)
Supplier: ENZO LIFE SCIENCES
Description: Peptide tyrosine-tyrosine (PYY) amide is a 36 amino-acid. PYY is a member of the pancreatic polypeptide (PP) family of peptides (neuropeptide Y (NPY), PYY and PP). While NPY is localized in neurons (both in the central and peripheral nervous system) and PP in the pancreatic islets, PYY is found in both neurons and the gut. PYY is released in response to food intake from the same endocrine cells (L cells) in the intestinal mucosa as the glucagon-like peptides, and inhibits gall bladder secretion, gut motility and pancreatic secretion. These effects are similar to those of PP and overlap with the gut inhibitory activity of GLP-1.
UOM: 1 * 1 mg

New Product


Catalog Number: (ENZOBMLFA0180050)
Supplier: ENZO LIFE SCIENCES
Description: Endogenous cannabinoid. Weak ligand of CB1 (Ki=23.8µM) and CB2 (Ki=13.9µM) receptor. Inhibits fatty acid amide hydrolase (FAAH) (IC50=5.1µM). Immunosuppressant, anti-inflammatory, anti-nociceptive and anti-convulsant in vivo. The exact mode of action has not yet been revealed. It has been suggested that PEA: i) binds to a yet to be discovered cannabinoid receptor similar to CB2; ii) administered in vivo elicits the synthesis of endogenous agonists of CB2; iii) acts as an "entourage" compound by enhancing the activity and/or by influencing the turnover of endogenous agonists of CB2, possibly but not uniquely, by inhibiting their degradation.
UOM: 1 * 50 mg

New Product


Catalog Number: (ENZOBMLEI3270025)
Supplier: ENZO LIFE SCIENCES
Description: URB-597 is a potent and selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), which is involved in the hydrolysis of endogenous cannabinoids such as anandamide. Inhibition of FAAH may serve to enhance the analgesic effects of endogenous cannabinoids. URB-597 has been shown to inhibit FAAH in rat cortical neuron membranes and in intact neurons with IC50 values of 4.6nM and 0.5nM, respectively. The compound has also been shown to have anxiolytic effects in rats (ID50=0.15mg/kg). Because URB-597 acts on FAAH and does not interfere with the binding of anandamide to the CB1 and CB2 receptors, it is a novel tool for drug development.
UOM: 1 * 25 mg

New Product


Catalog Number: (CAYM10005455-10)
Supplier: Cayman Chemical
Description: Arachidonoyl amides of both amino acids and neurotransmitters such as dopamine have been previously reported in the literature.
(1)N-Arachidonoyl-L-serine (ARA-S) is one such recently isolated endocannabinoid with an unusual activity profile. ARA-S does not bind to central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors or vanilloid receptor 1 (VR1). Like cannabidiol, ARA-S (5 mg/kg) antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model.
(2)However, similar to Abn-CBD, ARA-S relaxes isolated rat mesenteric arteries and abdominal aorta as well as increases phosphorylation of Akt and mitogen-activated protein kinase (MAPK) in HUVEC.
(3)The precise mechanisms of action by ARA-S and Abn-DBD in various vascular preparations appears to be different and requires further investigation.
UOM: 1 * 10 mg


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
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