Search results for "Propane-1"
showing 10 items of 196 documents
CCDC 1923203: Experimental Crystal Structure Determination
2020
Related Article: Abhisek Banerjee, Snehasis Banerjee, Carlos J. Gómez García, Samia Benmansour, Shouvik Chattopadhyay|2019|ACS Omega|4|20634|doi:10.1021/acsomega.9b02764
CCDC 1923202: Experimental Crystal Structure Determination
2020
Related Article: Abhisek Banerjee, Snehasis Banerjee, Carlos J. Gómez García, Samia Benmansour, Shouvik Chattopadhyay|2019|ACS Omega|4|20634|doi:10.1021/acsomega.9b02764
CCDC 699607: Experimental Crystal Structure Determination
2009
Related Article: M.Jung, A.Sharma, D.Hinderberger, S.Braun, U.Schatzschneider, E.Rentschler|2009|Eur.J.Inorg.Chem.||1495|doi:10.1002/ejic.200801248
CCDC 687036: Experimental Crystal Structure Determination
2011
Related Article: S.Banerjee, M.Nandy, S.Sen, S.Mandal, G.M.Rosair, A.M.Z.Slawin, C.J.G.Garcia, J.M.Clemente-Juan, E.Zangrando, N.Guidolin, S.Mitra|2011|Dalton Trans.|40|1652|doi:10.1039/c0dt00923g
Anthranilamide-based 2-phenylcyclopropane-1-carboxamides, 1,1'-biphenyl-4-carboxamides and 1,1'-biphenyl-2-carboxamides: Synthesis biological evaluat…
2017
Abstract Several anthranilamide-based 2-phenylcyclopropane-1-carboxamides 13a-f, 1,1’-biphenyl-4-carboxamides 14a-f and 1,1’-biphenyl-2-carboxamides 17a-f were obtained by a multistep procedure starting from the (1S,2S)-2-phenylcyclopropane-1-carbonyl chloride 11, the 1,1'-biphenyl-4-carbonyl chloride 12 or the 1,1'-biphenyl-2-carbonyl chloride 16 with the appropriate anthranilamide derivative 10a-f. Derivatives 13a-f, 14a-f and 17a-f showed antiproliferative activity against human leukemia K562 cells. Among these derivatives 13b, 14b and 17b exerted a particular cytotoxic effect on tumor cells. Derivative 17b showed a better antitumoral effect on K562 cells than 13b and 14b. Analyses perfo…
1-Aminocyclopropane-1-Carboxylic Acid, its Malonyl Conjugate and 1-Aminocyclopropane-1-Carboxylate Synthase Activity in Needles of Damaged and Undama…
1994
Summary Levels of free 1-aminocyclopropane-1-carboxylic acid (ACC), its malonyl conjugate (MACC) and ACC-synthase activity were significantly higher in the needles of damaged Norway spruce trees ( Picea abies (L.) Karst ) compared with those in undamaged trees during both the diurnal and seasonal courses. The concentrations of ACC and MACC, and ACC-synthase activity fluctuated much more intensively in the needles of damaged trees both in the diurnal and the seasonal courses than in those of undamaged ones, which implies that damaged trees respond more sensitively to the environmental conditions. ACC concentrations were the highest in summer and lowest in fall, while MACC concentrations seem…
CCDC 817805: Experimental Crystal Structure Determination
2011
Related Article: M.Sarwar, A.M.Madalan, F.Lloret, M.Julve, M.Andruh|2011|Polyhedron|30|2414|doi:10.1016/j.poly.2011.06.011
Changes of 1-Aminocyclopropane-1-Carboxylic Acid Oxidase Activity in Stressed Pinus Sylvestris Needles
2001
Stimulation of ethylene biosynthesis in pine needles by hydrogen peroxide and sodium bisulfite coincided with the activation of ACC oxidase at the level of protein synthesis. Decrease in ethylene production at high concentrations of sodium bisulfite (above 7 mM) was apparently due to inhibition of ACC oxidase activity. Treatment of pine needles with aminotriazole caused an inhibition of both ethylene production and ACC oxidase activity. Both methylviologen and methyl jasmonate stimulated ACC oxidase activity in a concentration-dependent manner with no parallel changes in ethylene production. The presented results suggest that ACC oxidase plays an important role in regulation of ethylene for…
CCDC 629530: Experimental Crystal Structure Determination
2007
Related Article: C.A.Jimenez, J.B.Belmar, F.S.Delgado, M.Julve, C.Ruiz-Perez|2007|CrystEngComm|9|746|doi:10.1039/b617605d
CCDC 949948: Experimental Crystal Structure Determination
2013
Related Article: Adrian E. Ion, Simona Nica, Augustin M. Madalan, Catalin Maxim, Miguel Julve, Francesc Lloret, Marius Andruh|2014|CrystEngComm|16|319|doi:10.1039/C3CE41592A