「AMIDE」の共起表現一覧(1語右で並び替え)
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| Pantetheine is the cysteamine | amide analogue of pantothenic acid (vitamin B5). |
| Structures are alternately bound via | amide and ester bridges. |
| idylamidoglycolate, and two products, peptidyl | amide and glyoxylate. |
| The interconversion of | amide and amine metabolites of 2-AAF can further occ |
| all but the most powerful bases such as sodium | amide and organo-sodium or lithium compounds. |
| logenation upon treatment with the base sodium | amide at 80 °C to produce cyclopropene in ~10% yield |
| are attached to the alpha-carbon atoms of the | amide backbone. |
| It is not as strong as | amide bases, e.g. |
| It is an | amide between glucosamine and acetic acid. |
| nlike nylon 6,6, in which the direction of the | amide bond reverses at each bond, all nylon 6 amide |
| m myristic acid) is covalently attached via an | amide bond to the alpha-amino group of an N-terminal |
| o the loss of electron delocalization when the | amide bond is twisted--this causes misalignment of t |
| cine motif in the activated ubiquitin forms an | amide bond to the epsilon amine of the lysine in the |
| rier protein), C(Condensation-formation of the | amide bond), and E(epimerization). |
| the primary amine at the N-terminus gives the | amide bond. |
| Chymotrypsin preferentially cleaves peptide | amide bonds where the carboxyl side of the amide bon |
| Chymotrypsin also hydrolyzes other | amide bonds in peptides at slower rates, particularl |
| idases) are a type of hydrolase that acts upon | amide bonds. |
| water which results in partial cleavage of the | amide bonds. |
| They produce as strong | amide bound than succinimidyl esters (SE, Hydroxysuc |
| They produce as strong | amide bound than succinimidyl esters (SE, Hydroxysuc |
| An acylhydrazine is analogous to an | amide, but the -OH portion of a carboxylic acid is r |
| ound this time he developed a keen interest in | amide chemistry. |
| N,O-Dimethylhydroxylamine is used in | amide coupling reactions to form Weinreb amides for |
| In comparison with its | amide derivative, iodoacetamide, iodoacetate reacts |
| bility of some of the more potent quinuclidine | amide derivatives in rat in vitro models have been l |
| Biocytin is a chemical compound that is an | amide formed from the vitamin biotin and the amino a |
| cyclic oligomers form when the nitrogen of the | amide forms a sigma bond to a lithium while the nitr |
| Isovaleramide is an | amide found in Valerian root. |
| thetic lacks not only the traditional ester or | amide function but the basic aliphatic nitrogen as w |
| omethyl group combine to sterically hinder the | amide functionality and provide both hydrolytic and |
| C(OH)< juncture between the two rings with the | amide functionality. |
| ylaminoethylchloride in the presence of sodium | amide gives chlorphenamine. |
| hat this molecule is very unstable because its | amide group has the amine lone pair and the carbonyl |
| Organic compounds of the | amide group can react in many different organic proc |
| The | amide group can further react with another amino gro |
| nitrile group in the obtained compound into an | amide group, and the subsequent acidic cyclization o |
| uting the carboxyl group in position 1 with an | amide group. |
| he most prominent feature of 2-pyridone is the | amide group; a nitrogen with a hydrogen bound to it |
| ide CaCl2) to occupy the hydrogen bonds of the | amide groups. |
| SAR studies for quinuclidine | amide have identified factors that are affecting the |
| f -0.42e and +0.20e to the carbonyl oxygen and | amide hydrogen, and the opposite charges to the carb |
| en bonds form between the backbone oxygens and | amide hydrogens. |
| Fatty acid | amide hydrolase or FAAH is a member of the serine hy |
| yme become potential substrates for fatty acid | amide hydrolase (FAAH), which hydrolyzes the free fa |
| ing the anandamide-degrading enzyme fatty acid | amide hydrolase (FAAH), thereby making it a useful t |
| t tissues and is inactivated by the fatty acid | amide hydrolase. |
| sition 8 to reduce asparagine rearrangement or | amide hydrolysis to aspartic acid, position 15 to en |
| For example, acetylene reacts with sodium | amide in liquid ammonia to form sodium acetylide, an |
| The suffixes -amine and | -amide in these names each refer to the single nitrog |
| Likewise, a similar derivative, dansyl | amide is known as DNSA. |
| n the nicotinamide structure, but in which the | amide is in the 4-position and not the 3-position. |
| Dansyl | amide is a reactive fluorescent dye that is used in |
| Lithium | amide is an inorganic compound with the chemical for |
| ed components, and while lysergic acid 2-butyl | amide is more potent than LSD as a 5-HT1A agonist, i |
| oined by an ester linkage, the opposite of the | amide linkage found in anandamide. |
| ptide-derived cyclol-lactam ring connected via | amide linkage to a lysergic acid (ergoline) moiety, |
| ich the ring attaches to various scaffolds via | amide linkages. |
| Cinchocaine (or Dibucaine) is an | amide local anesthetic. |
| opyllysergamide (lysergic acid methylisopropyl | amide, MIPLA) is an analogue of LSD that was origina |
| ve as activated components for construction of | amide moieties. |
| ames should be R1 (indole-1 position), Ramide ( | amide N-substituent)... Cacycle 19:24, 27 Mar 2005 ( |
| somer of LSD, with the two ethyl groups on the | amide nitrogen having been replaced by a single buty |
| al isomer of LSD, with the alkyl groups on the | amide nitrogen having been subjected to a methylene |
| at elevated temperatures to the corresponding | amide o-Salicylotoluide . |
| It is the | amide of propanoic acid. |
| Butyramide is the | amide of butyric acid. |
| Oleamide is an | amide of the fatty acid oleic acid. |
| It is an | amide of pelargonic acid and vanillylamine. |
| name for the substance o-hydroxybenzamide, or | amide of salicyl. |
| Noflan is a complex of the | amide of alkylphosphonic acid ammonium salt with amm |
| N-Oleoylethanolamine is the | amide of oleic acid (18:1) and ethanolamine. |
| N-Palmitoylethanolamine is the | amide of palmitic acid (16:0) and ethanolamine. |
| This colourless solid is a lactam or a cyclic | amide of caproic acid. |
| abbreviated HMPA, is a phosphoramide (i.e. an | amide of phosphoric acid) having the formula [(CH3)2 |
| ocess of exchanging the subunits of a peptide, | amide or ester compound with another amine or fatty |
| residue of the protein (except proline) has an | amide proton attached to a nitrogen in the peptide b |
| es; it therefore appears that formation of the | amide similarly involves the intermediate anhydride, |
| This relatively simple process uses only one | amide solvent, and therefore spinning can be done di |
| en bonds as acid-D-ammonia (or amine) ligases ( | amide synthases). |
| The direct amination of pyridine with sodium | amide takes place in liquid ammonia. |
| If the starting material is an α-halo | amide, the product is an α,β-epoxy amide. |
| Chemically, it is an | amide union of parachlorophenoxyacetate and methylen |
| uct with benzoyl chloride gives the respective | amide, which cyclizes into the desired medazepam usi |
| nitrile or by treating tetrachloroisophthaloyl | amide with phosphoryl chloride. |
| llner process involving the reaction of sodium | amide with carbon at elevated temperatures. |
| Pederin is a vesicant toxic | amide with two tetrahydropyran rings, found in the h |
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