Examples of using Amide in English and their translations into Malay
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Consequently, the nitrogen in amides is not pyramidal.
Both amides and nitride(N3-) salts are known, but decompose in water.
It is free from organic contamination such as silicone, phthalate, or amide.
For discussion of these"anionic amides", see Alkali metal amides.
Liquid ammonia is in fact slightly amphiprotic andforms ammonium and amide ions(NH2-);
Amides are also commonly derived from secondary amines(R'R''NH) with the formula RC(O)NR'R''.
Oolong also contains detoxifying alkaloids such as niacin amide and folic acid.
Tertiary amides are commonly derived from secondary amines(R′R″NH) and have the general structure RC(O)NR′R″.
Aminopyridine can continue achieved when sodium amide is used as the nucleophile.
Anti-static Foam Tipped Swab FS746 isfree from organic contamination such as silicone, amide.
Anti-Static Swab Stick PS743 is free from silicone and amide, it is acid and solvent resistant.
Clean Room Microfiber Swab MS758is free from organic contamination like silicone and amide.
Amide Alcohol Antibiotics has a certain immunosuppressive effect when used above the recommended dose.
It is made of repeatingunits linked by peptide bonds(another name for amide bonds) and is frequently referred to as polyamide(PA).
Amide can also refer to the conjugate base of ammonia(the anion H 2 N-) or of an organic amine(an anion R 2 N-).
Closely related and even more numerous are secondary amides which can be derived from primary amines(R′NH2) and have the formula RC(O)NHR′.
Amide can also refer to azanide(the anion H2N-, conjugate base of ammonia) or to an organic amine(an anion R2N-).
Foam Cleaning Swabs FS741 is laundered in class 10 cleanroom facility, bonded by thermal heat minimize contamination level,free from organic contaminants such as silicone and amide.
Raw Palmitoylethanolamide powder(PEA) is an endogenous fatty acid amide, belonging to the class of nuclear factor agonists.
Given the known metabolic liberation(and presence as an impurity) of amantadine in the related compound APINACA,it is suspected that metabolic hydrolysis of the amide group of APICA may also release amantadine.
An amide is characterized by the presence of a functional group known as R n E(O) x NR′2(R and R′ refer to H or organic groups).
JW642is selective for MAGL,requiring much higher concentrations to effectively inhibit fatty acid amide hydrolase activity(IC50s= 31, 14, and 20.6 µM for mouse, rat, andhuman brain membranes, respectively).
An amide( or or), also known as an acid amide, is a compound with the functional group RnE(O)xNR′2(R and R′ refer to H or organic groups).
JZL-184 is a potent and selective inhibitor of monoacylglycerol lipase(MAGL) that displays IC50 values of 8 nM and 4 µM for inhibition of MAGL andfatty acid amide hydrolase in mouse brain membranes, respectively.
Amide are usually regarded as derivatives of carboxylic acids in which the hydroxyl group has been replaced by an amine or ammonia.
Foam Cleaning Swabs FS742 is washed by D.I water system and processed in class 10 cleanroom facility, thermal bond technique produce no adhesive contamination,it is free from organic contaminants such as silicone and amide.
Anandamide is predominantly metabolized by fatty acid amide hydrolase(FAAH), whereas monoacylglycerol lipase(MAGL) is thought to be the enzyme primarily responsible for the degradation of 2-AG.
Raw Pramiracetam powder(also known as Pramistar) is a cognitive enhancer(nootropic) that is synthesized from piracetam, the original racetam,by substituting the amide group in piracetam with a dipropan-2-ylamino ethyl group.
Oil auxiliaries gemini quaternary ammonium saltProducts basic information Product name Amide based Gemini quaternary ammonium salt Technology brief This product is a new type of Gemini quaternary ammonium salt has the dual active site it adopts….
URB597, also known as KDS-4103,is a highly potent and selective inhibitor of fatty-acid amide hydrolase(FAAH), an enzyme catalyzing the intracellular hydrolysis of the endocannabinoid anandamide, with values of 50% inhibition concentration IC50 of 4.6 nM and 0.5 nM in rat brain membranes and human liver microsomes respectively.