「-amine」の共起表現一覧(1語右で並び替え)
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| Amine absorption | |
| ry Fast Death Factor, is a secondary, bicyclic | amine alkaloid and cyanotoxin with acute neurotoxici |
| e:beta-D-galactosyl-1,4-N-acetyl-beta-D-glucos | amine alpha-2,6-N-acetylneuraminyltransferase. |
| The suffixes | -amine and -amide in these names each refer to the si |
| It contains both a primary | amine and a primary alcohol. |
| 5), soluble in ammonia, | amine and EDTA solutions under complex formation. |
| Other | amine and neuropeptide neurotransmitters may also in |
| of nitro group reduction, diazotization of the | amine, and hydrolysis. |
| uclidine is an organic compound and a bicyclic | amine and used as a catalyst and a chemical building |
| benzaldehyde is an organic compound containing | amine and aldehyde moieties which is used in Ehrlich |
| nternal hydrogen bond between the neighbouring | amine and hydroxyl groups that partly co-ordinates w |
| free base refers to the pure basic form of an | amine, as opposed to its salt form. |
| ut only the nucleophilic attack of the primary | amine at the N-terminus gives the amide bond. |
| Tetramethylguanidine is a strong | amine base with a higher pKa than typical amines, th |
| Selexol usually requires less energy than the | amine based processes. |
| Selexol is a physical solvent, unlike | amine based acid gas removal solvents that rely on a |
| rbed per volume of solvent) is reduced and the | amine based processes will usually be superior. |
| Abou Abderahmane | Amine, born Djamel Zitouni (January 5, 1964, Les Euc |
| a para-diamine with two molecules of a primary | amine; by the condensation of para-aminoazo compound |
| The protected | amine can be deprotected by catalytic hydrogenation |
| eaction is pH dependent because the protonated | amine cannot cyclize. |
| s by cascaded chemical exchange reactions with | amine carbamate. |
| mation pathways for arylamine and heterocyclic | amine carcinogens |
| ures could be employed with the presence of an | amine catalyst. |
| r storage than the relatively unstable primary | amine cathinone derivatives. |
| This | amine combined with Lewis acidic iron centers makes |
| Reduction to a secondary | amine completes the synthesis of (6). |
| metal ions in solution such as Fe2+ or a Cu2+ | amine complex. |
| The choice of | amine concentration in the circulating aqueous solut |
| This heterocyclic | amine consists of a six-membered ring containing fiv |
| Other names in common use include aromatic | amine dehydrogenase, dehydrogenase, arylamine, tyram |
| is a molecule required for the functioning of | amine dehydrogenase. |
| e to the formyl 4 and in a Mannich reaction to | amine derivative 4 |
| ther 1-methylated-ergoloids to their secondary | amine derivatives has been frequently noted in mamma |
| nohexahydrobenzene, is an organic chemical, an | amine derived from cyclohexane. |
| es a nucleophilic catalyst, usually a tertiary | amine, for a Michael-type addition and elimination. |
| d pharmaceuticals to describe the unprotonated | amine form of a compound. |
| Polyaspartic esters are a new type of | amine functional coreactant for aliphatic polyisocya |
| In the first step, the | amine functional group is diazotized with hydrochlor |
| Hexane-2,5-dione reacts with the | amine functional group; for example the amine group |
| ols are organic compounds that contain both an | amine functional group and an alcohol functional gro |
| ecule containing at least one carboxyl and two | amine functional groups. |
| simple and inexpensive synthesis from primary | amine functionalized (chiral-pool) starting material |
| mpurities to acceptable levels, commonly by an | amine gas treating process. |
| r more information, see: Hydrodesulfurization, | Amine gas treating, and Merox |
| Former president Sheikh | Amine Gemayel for the Kataeb Party (March 14 Allianc |
| e March 14 Alliance, alongside Saad Hariri and | Amine Gemayel. |
| cal formula C6N6O12, obtained by oxidizing the | amine group of pentanitroaniline with hydrogen perox |
| Amino acids containing a secondary | amine group (the only proteinogenic amino acid of th |
| ymine as it is identical to adenine but has an | amine group at position 2 forming 3 intramolecular h |
| (Note | amine group at bottom right.) |
| It can be used to exchange the oxygen for an | amine group on the carbonyl carbon of aldehydes or k |
| osamines are amino sugars created by adding an | amine group to a hexose. |
| Deamination is the removal of an | amine group from a molecule. |
| The | amine group in the aminoallyl moiety is aliphatic an |
| Because that substance contained an | amine group, he called it vitamine. |
| of an enone, with the carbonyl replaced by an | amine group. |
| achment of phosphoribosyl pyrophosphate to the | amine group. |
| ermination of amino acids containing a primary | amine group. |
| sulfate anion, the collagen's carboxyl groups, | amine groups from the side chains of the amino acids |
| It is known that the | amine groups (nitrogen atom bonded to carbon and or |
| This derivative is reactive towards | amine groups on proteins inside cells. |
| nding on stoichiometry ) reacts with available | amine groups to so-called N-sulfinic acid groups. |
| e tails are normally positively charged due to | amine groups present on their lysine and arginine am |
| n containing phosphate buffer as Tris contains | amine groups). |
| is is called an O-hydroxylamine, if one of the | amine hydrogens is substituted, this is called an N- |
| is a derivative of phenylarsonic acid with an | amine in the 4-position. |
| If a primary | amine is present, the isocyanide is formed. |
| Polyethylene | amine is a polymer based on aziridine monomer. |
| The | amine is usually an alkaloid natural product. |
| Polyethylene | amine is a polymer of aziridine with the molecular f |
| The | amine is liberated by addition of sodium hydroxide a |
| ugate base resulting from deprotonation of the | amine is rarely observed. |
| An aromatic | amine is an amine with an aromatic substituent - tha |
| This aromatic | amine is a component of a test for cyanide and also |
| The | amine is basic and undergoes quaternization with met |
| ng it with hydrogen with a nickel catalyst; an | amine is formed in this reaction (see nitrile reduct |
| ned alkaline using sodium hydroxide before the | amine is extracted using CH2Cl2. |
| s highly basic and unhindered, although, as an | amine it is considered a weak base. |
| Mohamed | Amine Khamsi is an American/Moroccan mathematician. |
| Moroccan | Amine Laalou won the first semi-final, followed by A |
| As a tertiary | amine, Laudanosine is unionised and readily crosses |
| rate contains three platinum centres linked by | amine ligands. |
| ng carbon-nitrogen bonds as acid-D-ammonia (or | amine) ligases (amide synthases). |
| Hindered | amine light stabilisers (HALS) stabilise against wea |
| It is also a secondary | amine like methamphetamine, and forms salts in the s |
| e a cyclopropyl group into ester, sulfate, and | amine linkages. |
| not the phosphorus lone pair (as in imines the | amine lone pair) but the double bond. |
| very unstable because its amide group has the | amine lone pair and the carbonyl group not properly |
| belongs to the family of lyases, specifically | amine lyases, which cleave carbon-nitrogen bonds. |
| In both cases, the salt forms of the | amine makes these otherwise lipophilic compounds wat |
| Polyethylene | amine may have applications as a component of ion ex |
| Similarly a chiral | amine may also be used to achieve stereoselectivity. |
| The interconversion of amide and | amine metabolites of 2-AAF can further occur via the |
| s: indolethylamine N-methyltransferase (INMT), | amine N-methyltransferase, arylamine N-methyltransfe |
| on use include arylamine sulfotransferase, and | amine N-sulfotransferase. |
| azid included, increase the levels of biogenic | amine neurotransmitters found within the brain and a |
| It is an analogue of dichloropane where the | amine nitrogen has been replaced by an oxygen ether |
| ture results in some double methylation of the | amine nitrogen, yielding MDDM as well as MDMA. |
| ramolecular trapping of episulfonium ions with | amine nucleophiles and the use of triisopropylsilyl |
| the alpha carboxyl of one residue to the alpha | amine of another). |
| d ubiquitin forms an amide bond to the epsilon | amine of the lysine in the modified protein. |
| nal group over the, now diminished, quaternary | amine of this surface chemistry to separate the phos |
| It is a sympathomimetic | amine of the 3-hydroxy-phenylethanolamine series use |
| is an endogenous monoamine compound and trace | amine of the phenethylamine class. |
| If the | amine on the Adrenergic agent has a substituent bigg |
| methoxide leads first to the ionization of the | amine on the side chain; this then cyclizes to a tri |
| peptide, amide or ester compound with another | amine or fatty acid to produce a new amide or peptid |
| tra-molecular hydrogen bonding of its tertiary | amine, or perhaps yuremamine acts as a prodrug and r |
| nd with two carbonyl groups bound to a primary | amine or ammonia. |
| can refer to any of the six isomers of xylene | amine, or any mixture of them. |
| d, to a lesser extent, semicarbazide-sensitive | amine oxidase (SSAO), as well as a serotonin releasi |
| Amine oxidase is an enzyme involved in the metabolis | |
| Copper-containing | amine oxidases are found in bacteria, fungi, plants |
| s aspergillus and in bacteria the main role of | amine oxidases is to provide a source of ammonium. |
| General structure of an | amine oxide |
| The more stable tautomer is the | amine oxide form. |
| In the strict sense the term | amine oxide applies only to oxides of tertiary amine |
| n as dodecyldimethylamine oxide or DDAO, is an | amine oxide surfactant. |
| s a heterocycle of the isoxazole family and an | amine oxide derivative of furazan. |
| cal compound which can be used as a nitroxide ( | amine oxide) paramagnetic spin label in protein Elec |
| dative bond, as is currently used to depict an | amine oxide. |
| Amine oxides are used as protecting group for amines | |
| Long-chain alkyl | amine oxides are used as nonionic surfactants and fo |
| Amine oxides of anti-cancer drugs have been develope | |
| Amine oxides are prepared by oxidation of tertiary a | |
| Amine oxides are weak bases with a pKa of around 4.5 | |
| Examples of | amine oxides include pyridine N-oxide, a water-solub |
| d sulfones, and oxidation of amines to produce | amine oxides. |
| Flavin-containing | amine oxidoreductases are a family of various amine |
| rine with diethylamine gives the corresponding | amine oxolamine. |
| stimate its basicity in an experiment in which | amine pairs (the quinuclidonium salt and a reference |
| light products plants, polymerization plants, | amine plants, sulfur plants, and impurities treatmen |
| es two methylations by SAM at the hydroxyl and | amine position. |
| l cells therefore belong to the group of APUD ( | amine precursor uptake and decarboxylation) cells. |
| eaction allows phthalimide anion to be used as | amine precursor in the Gabriel synthesis. |
| Precursor Uptake - for high uptake of ( | amine) precursors. |
| rformance and environmental constraints of the | amine process, a newer technology based on the use o |
| ch one of the oxygen atoms is replaced with an | amine, producing a non-hydrolyzable functional group |
| which on a double Mitsunobu reaction (with an | amine proton donor) gives the azafenestrane 10 as th |
| Pro7, whose real name is | Amine Rachad is a French electro-music producer and |
| which the lone pair of electrons on a primary | amine react with the carbonyl carbon of an aldehyde. |
| this gene is most closely related to biogenic | amine receptors. |
| respectable woman equals a silent woman - but | Amine refuses to abide by such rules. |
| Crystalline forms are obtained as the | amine salt by reacting the free base with a mineral |
| For the heterocyclic | amine, see Tetrahydroisoquinoline. |
| OPA reacts also with thiols in presence of an | amine such as n-propylamine or 2-aminoethanol. |
| e presence of a large excess of a coordinating | amine such as pyridine which presumably binds to lea |
| In enzymology, an | amine sulfotransferase (EC 2.8.2.3) is an enzyme tha |
| fragment of the substrate is released with an | amine terminus, the histidine residue in the proteas |
| rboline (9H-pyrido[3,4-b]indole) is an organic | amine that is the prototype of a class of compounds |
| 3] + Bu3N Bu3NH+ [P(O2C6Cl4)3]- Using a chiral | amine, the anion can be readily resolved. |
| As a primary | amine, the dye can be diazotized in the laboratory, |
| This | amine then reacts with another isocyanate group to f |
| ethyl ether), the epoxide is opened with allyl | amine to yield the corresponding 1,2-amino alcohol. |
| a single covalent bond (such as protonating an | amine to form an ammonium center or removing a hydri |
| Amine Touahri | |
| Other names in common use include | amine transaminase, amine-ketoacid transaminase, dia |
| (18) vesicular | amine transporter |
| ) are used as a gas stream scrubbing liquid in | amine treaters. |
| that purpose as shown in the flow diagram, but | amine treating is the process that was historically |
| ly H2S concentrated gas, the by-product of the | amine treatment plant, can be recompressed by compre |
| As a trifunctional | amine, tren forms a triisocyanate when derivatized w |
| rade name Aramine) is a potent sympathomimetic | amine used in the prevention and treatment of hypote |
| norepinephrine (α-Me-NE), is a sympathomimetic | amine used as a topical nasal decongestant and vasoc |
| It is thought that the | amine weakens the C-N bond in the nitromethane, resu |
| es of this enzyme are ATP, H2O, and quaternary | amine, whereas its 3 products are ADP, phosphate, an |
| this enzyme are 3'-phosphoadenylyl sulfate and | amine, whereas its two products are adenosine 3',5'- |
| ne is a tertiary (a highly hindered) aliphatic | amine which has antihypertensive effects. |
| 4,4'-Thiodianiline (TDA) is an aromatic | amine which is presumed to be carcinogenic to humans |
| reason to believe that this central atom is an | amine which functions as a Lewis base. |
| The choice of the type of | amine will affect the required circulation rate of a |
| Diethylamine is a secondary | amine with the molecular structure CH3CH2NHCH2CH3. |
| Tetrahydroisoquinoline is a secondary | amine with the chemical formula C9H11N. |
| amine is an organic compound (specifically, an | amine) with the formula CH3CH2CH2CH2NH2. |
| ropylamine, also known as n-propylamine, is an | amine with the chemical formula C3H9N. |
| This group can be regarded as a secondary | amine with a cyano substituent. |
| Bis-tris is an organic tertiary | amine with labile protons having a pKa of 6.46 at 25 |
| an organic chemical compound (specifically, an | amine) with the formula (CH3)3CNH2, and occurs as a |
| ine is a biochemical compound consisting of an | amine with a β-N-glycosidic bond to a carbohydrate, |
| As the product of polymerization is an | amine with a basic character, the reaction is self-c |
| an organic chemical compound (specifically, an | amine) with the formula CH3CH2CH(NH2)CH3, and occurs |
| e isonitrile can be obtained by reacting ethyl | amine with chloroform (note that the fume hood is re |
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