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1 g the plausible prebiotic condensing reagent cyanamide.
2 blocked by 4-methylpyrazole and augmented by cyanamide.
3 the alcohol deterrent agents, disulfiram and cyanamide.
4 ycloaddition of two terminal alkynes and one cyanamide.
5 oviding N-(1H-pyrrolo[3,2-c]isoquinolin-5-yl)cyanamides.
6            These species yield the tricyclic cyanamides [1,2,3]triazolo[1,5-a]quinoxaline-5(4H)-carbo
7                             Carbodiimide 10, cyanamide 12, N-cyanomethyleneimine 13, and its protonat
8 rium before and 30 minutes after infusion of cyanamide (17 mg/kg), an inhibitor of mtALDH.
9 w marked differences: formation of the amino cyanamide 4 (H2N-N(CH3)-C identical withN) is only obser
10 trile imines, while observation of the amino cyanamide 4 represents a novel reaction pathway in the p
11 en in Lafora's disease (myoclonus epilepsy), cyanamide alcohol aversion therapy, and type IV glycogen
12 [4 + 2] cycloaddition of indolylynamides and cyanamides (aminonitriles) is an efficient redox-neutral
13                              The presence of cyanamide (an inhibitor of aldehyde dehydrogenase) in th
14 (AR) inhibitor, attenuated GS-DHN levels and cyanamide, an aldehyde dehydrogenase inhibitor, decrease
15 ted A1DH directly, or spontaneously released cyanamide, an inhibitor of A1DH.
16 in the coronary effluent, and treatment with cyanamide, an inhibitor of aldehyde dehydrogenase, atten
17 th pyruvate, an NADH-oxidizing compound, and cyanamide, an inhibitor of aldehyde dehydrogenase, signi
18 he Pd(0)-catalyzed carbonylative coupling of cyanamide and aryl iodides or bromides.
19  various N-substituted o-halobenzamides with cyanamide and formamide, respectively.
20 rowia lipolytica to assimilate nitrogen from cyanamide and phosphorus from potassium phosphite, and t
21  between the cyano group of the intermediate cyanamides and the azide anion.
22  prebiotic conditions using histidine (His), cyanamide, and 4-amino-5-imidazole carboxamide.
23  (1) or of 2-aminoquinazolines (2) involving cyanamides, arylboronic acids, and amines has been devel
24 m iron acetate as an iron precursor and from cyanamide as a nitrogen and carbon nanotube precursor in
25  rat liver microsomes and NADPH gave rise to cyanamide as metabolite, identified as its dansylated de
26 nt one-pot cyclo-guanidinylation of 10 using cyanamide as the guanidinylating agent.
27  using short aminonitriles (dicyandiamide or cyanamide) as shape controlling agents.
28 core of nagelamide W from alkene 6 through a cyanamide bromide intermediate.
29                                              Cyanamides can be easily reduced to 1H-pyrrolo[3,2-c]iso
30 -Diels-Alder cycloaddition of enynamides and cyanamides comprises an efficient route to diversely sub
31     The starting materials for the synthesis-cyanamide, cyanoacetylene, glycolaldehyde, glyceraldehyd
32 ltured in the presence of the ALDH inhibitor cyanamide/disulfiram and subjected to oxidative stress d
33 des isomerize thermally to the corresponding cyanamides (e.g., Ph-N horizontal lineC horizontal lineN
34 nd octahydroisoindole small molecules with a cyanamide electrophile that forms a covalent bond with a
35 ermore, the aldehyde dehydrogenase inhibitor cyanamide enhanced the effect of ethanol in the hepatoma
36 of readily available ortho-iodoanilines with cyanamide followed by in situ ring closure of an N-cyano
37 1-phosphate (G1P) and ATP in the presence of cyanamide for 24 h at 70 degrees C.
38                                              Cyanamide formation was minimal in the absence of coenzy
39                         The formation of the cyanamides from isomeric pyrrolo[3,2-c][1,2,4]triazolo[3
40  a biohybrid platform that is assembled from cyanamide-functionalized carbon nitride (CN(X)) as a sca
41                        Ni(2)P synthesized on cyanamide-functionalized carbon nitride is shown to prom
42                                        Here, cyanamide-functionalized CN(x) ((NCN) CN(x) ) was co-dep
43      This radical species is formed within a cyanamide-functionalized polymeric network of heptazine
44 n of a carbon nitride polymer populated with cyanamide groups, yielding a material with 12 and 16 tim
45                   The formation of tricyclic cyanamides has been examined by experimental and computa
46 ubstituted vinyl nitriles, thiocyanates, and cyanamides have all been shown to be viable substrates f
47 e proteins are also stabilized upon hydrogen cyanamide (HC) application under normoxic conditions, an
48 ted that dormancy-breaking compound hydrogen cyanamide (HC) stimulates the fermentative pathway and i
49 gen sulfide, water, methanol, hydroxylamine, cyanamide, hydrazine and methylhydrazine to the 5-cyano
50 ent of a range of (het)aryldithioesters with cyanamide in the presence of NaH, followed by in situ S-
51 ents, subsequently converting into the final cyanamide in the rate-determining step.
52 e formed from beta-mercapto-acetaldehyde and cyanamide in water at neutral pH.
53 yl (HN=O), the putative active metabolite of cyanamide, in inhibiting aldehyde dehydrogenase (AlDH).
54 s with the aldehyde dehydrogenase inhibitor, cyanamide, increased the levels of acetaldehyde and resu
55 nted by the aldehyde dehydrogenase inhibitor cyanamide, indicating that acetaldehyde was responsible
56 5-amino-1,3-diaryl-1H-pyrazol-4-yl)methylene]cyanamide is the intermediate.
57 n, the use of N-substituted nitriles, namely cyanamides, leads to the facile generation of difficult-
58 -C bond formation resulting in a substituted cyanamide ligand.
59                                          The cyanamide-mediated production of CDP-ethanolamine was ca
60 that a well-defined triplet excited state in cyanamide-modified carbon nitride is realized with appro
61 tazine-based model catalysts to identify the cyanamide moiety as a photocatalytically relevant 'defec
62 te the ultrafast hydration dynamics around a cyanamide (NCN) probe attached to a nucleoside, deoxycyt
63 aled containers), coupled to the presence of cyanamide (NCNH(2)) and portlandite (Ca(OH)(2)) in these
64  or 5-amino-1H-pyrazole-4-carbaldehydes with cyanamide (NH(2)C=N) in an acid-mediated solution.
65 use of high-energy organic compounds such as cyanamide or hydrogen cyanide.
66 and short periods of time, with mediation by cyanamide or urea.
67 ed [2 + 2 + 2] cycloadditions with nitriles, cyanamides, or isocyanates in the presence of CpCo(CO)2
68 t deactivation occurs with a large excess of cyanamide over longer reaction times.
69  (11)C-CNS 5161 [N-methyl-3(thyomethylphenyl)cyanamide] positron emission tomography, a marker of act
70                                              Cyanamide reacts especially rapidly with ribose to form
71 es starting from aryl- or benzyl-substituted cyanamides, respectively.
72                                              Cyanamide significantly inhibited both the classic dehyd
73 or-is readily formed from glycolaldehyde and cyanamide, so is 2-aminothiazole formed from beta-mercap
74 zothiazole and S-arylation to give the ortho-cyanamide-substituted diaryl thioether intermediate.
75                                              Cyanamide surface functionalized melon-type carbon nitri
76                       Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitri
77                B(C6F5)3 activates N-sulfonyl cyanamides, thus leading to a formal cleavage of the N-C
78 o used to cyclize two terminal alkynes and a cyanamide to afford a 2,4,6-trisubstituted pyridine prod
79                                   Diynes and cyanamides undergo an iron-catalyzed [2 + 2 + 2] cycload
80 the presence of additives such as formamide, cyanamide, urea, guanidine, 2-aminoimidazole, and hydant
81 atalyzed annulation; in the second approach, cyanamide was used unprecedently as an amine component i
82   A cascade radical cyclization of alkenyl N-cyanamides with aromatic aldehydes has been achieved for
83 nc oxide (ZnO) when heated in air or to zinc cyanamide (ZnCN(2)) when heated in an inert atmosphere.