ライフサイエンスコーパス: cyanamide

1 ycloaddition of two terminal alkynes and one cyanamide.

2 g the plausible prebiotic condensing reagent cyanamide.

3 blocked by 4-methylpyrazole and augmented by cyanamide.

4 the alcohol deterrent agents, disulfiram and cyanamide.

5 oviding N-(1H-pyrrolo[3,2-c]isoquinolin-5-yl)cyanamides.

6 Carbodiimide 10, cyanamide 12, N-cyanomethyleneimine 13, and its protonat

7 rium before and 30 minutes after infusion of cyanamide (17 mg/kg), an inhibitor of mtALDH.

8 w marked differences: formation of the amino cyanamide 4 (H2N-N(CH3)-C identical withN) is only obser

9 trile imines, while observation of the amino cyanamide 4 represents a novel reaction pathway in the p

10 en in Lafora's disease (myoclonus epilepsy), cyanamide alcohol aversion therapy, and type IV glycogen

11 The presence of cyanamide (an inhibitor of aldehyde dehydrogenase) in th

12 (AR) inhibitor, attenuated GS-DHN levels and cyanamide, an aldehyde dehydrogenase inhibitor, decrease

13 ted A1DH directly, or spontaneously released cyanamide, an inhibitor of A1DH.

14 in the coronary effluent, and treatment with cyanamide, an inhibitor of aldehyde dehydrogenase, atten

15 th pyruvate, an NADH-oxidizing compound, and cyanamide, an inhibitor of aldehyde dehydrogenase, signi

16 he Pd(0)-catalyzed carbonylative coupling of cyanamide and aryl iodides or bromides.

17 rowia lipolytica to assimilate nitrogen from cyanamide and phosphorus from potassium phosphite, and t

18 prebiotic conditions using histidine (His), cyanamide, and 4-amino-5-imidazole carboxamide.

19 (1) or of 2-aminoquinazolines (2) involving cyanamides, arylboronic acids, and amines has been devel

20 m iron acetate as an iron precursor and from cyanamide as a nitrogen and carbon nanotube precursor in

21 rat liver microsomes and NADPH gave rise to cyanamide as metabolite, identified as its dansylated de

22 nt one-pot cyclo-guanidinylation of 10 using cyanamide as the guanidinylating agent.

23 using short aminonitriles (dicyandiamide or cyanamide) as shape controlling agents.

24 Cyanamides can be easily reduced to 1H-pyrrolo[3,2-c]iso

25 The starting materials for the synthesis-cyanamide, cyanoacetylene, glycolaldehyde, glyceraldehyd

26 ltured in the presence of the ALDH inhibitor cyanamide/disulfiram and subjected to oxidative stress d

27 des isomerize thermally to the corresponding cyanamides (e.g., Ph-N horizontal lineC horizontal lineN

28 ermore, the aldehyde dehydrogenase inhibitor cyanamide enhanced the effect of ethanol in the hepatoma

29 of readily available ortho-iodoanilines with cyanamide followed by in situ ring closure of an N-cyano

30 1-phosphate (G1P) and ATP in the presence of cyanamide for 24 h at 70 degrees C.

31 Cyanamide formation was minimal in the absence of coenzy

32 The formation of the cyanamides from isomeric pyrrolo[3,2-c][1,2,4]triazolo[3

33 This radical species is formed within a cyanamide-functionalized polymeric network of heptazine

34 n of a carbon nitride polymer populated with cyanamide groups, yielding a material with 12 and 16 tim

35 ubstituted vinyl nitriles, thiocyanates, and cyanamides have all been shown to be viable substrates f

36 ted that dormancy-breaking compound hydrogen cyanamide (HC) stimulates the fermentative pathway and i

37 gen sulfide, water, methanol, hydroxylamine, cyanamide, hydrazine and methylhydrazine to the 5-cyano

38 e formed from beta-mercapto-acetaldehyde and cyanamide in water at neutral pH.

39 yl (HN=O), the putative active metabolite of cyanamide, in inhibiting aldehyde dehydrogenase (AlDH).

40 s with the aldehyde dehydrogenase inhibitor, cyanamide, increased the levels of acetaldehyde and resu

41 nted by the aldehyde dehydrogenase inhibitor cyanamide, indicating that acetaldehyde was responsible

42 -C bond formation resulting in a substituted cyanamide ligand.

43 The cyanamide-mediated production of CDP-ethanolamine was ca

44 tazine-based model catalysts to identify the cyanamide moiety as a photocatalytically relevant 'defec

45 use of high-energy organic compounds such as cyanamide or hydrogen cyanide.

46 and short periods of time, with mediation by cyanamide or urea.

47 ed [2 + 2 + 2] cycloadditions with nitriles, cyanamides, or isocyanates in the presence of CpCo(CO)2

48 t deactivation occurs with a large excess of cyanamide over longer reaction times.

49 (11)C-CNS 5161 [N-methyl-3(thyomethylphenyl)cyanamide] positron emission tomography, a marker of act

50 Cyanamide reacts especially rapidly with ribose to form

51 es starting from aryl- or benzyl-substituted cyanamides, respectively.

52 Cyanamide significantly inhibited both the classic dehyd

53 or-is readily formed from glycolaldehyde and cyanamide, so is 2-aminothiazole formed from beta-mercap

54 Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitri

55 B(C6F5)3 activates N-sulfonyl cyanamides, thus leading to a formal cleavage of the N-C

56 o used to cyclize two terminal alkynes and a cyanamide to afford a 2,4,6-trisubstituted pyridine prod

57 Diynes and cyanamides undergo an iron-catalyzed [2 + 2 + 2] cycload

58 nc oxide (ZnO) when heated in air or to zinc cyanamide (ZnCN(2)) when heated in an inert atmosphere.