Results 11 to 20 of about 7,864 (178)
Structure-activity relationship study shows versatility in substrate specificity for heterodisulfide reductase in methanogenic archaea. [PDF]
Protein SciAbstract Hydrogenotrophic methanogens are anaerobic archaea that convert carbon dioxide and hydrogen into methane. Central to this process is the heterodisulfide reductase (Hdr), which catalyzes the reduction of the heterodisulfide made of coenzyme M and coenzyme B. In vivo, Hdr functions in association with electron‐donating modules such as the [NiFe]‐
Maleki MF +5 more
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1,3-Dicyclohexyl-1-isonicotinoylurea monohydrate
Acta Crystallographica Section E, 2008 The title organic compound, C19H27N3O2·H2O, was synthesized from methylene dicyclohexylamine, 4-pyridinecarboxylic acid and N,N′-dicyclohexylcarbodiimide.
Cun-Kuan Wang, Feng-Yan Zhou
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N-(2-(1H-Indol-3-yl)ethyl)-2-(2-fluoro-[1,1′-biphenyl]-4-yl)propanamide
Molbank, 2020 N-(2-(1H-Indol-3-yl)ethyl)-2-(2-fluoro-[1,1′-biphenyl]-4-yl)propanamide was prepared by a reaction between tryptamine and flurbiprofen, applying N,N’-Dicyclohexylcarbodiimide, as a coupling agent.
Stanimir Manolov +2 more
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Interactions of dicyclohexylcarbodiimide with myelin proteolipid. [PDF]
Proceedings of the National Academy of Sciences, 1982 Dicyclohexylcarbodiimide (DCCD) is known to bind preferentially to a proteolipid subunit of proton-translocating systems and thereby to inhibit proton transport. In the present study we show that, in an aqueous medium, DCCD binds to the bovine white matter proteolipid apoprotein, the major protein of central nervous system myelin.
L F, Lin, M B, Lees
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Synthesis of the Key Precursor of Hirsutellide A
Molecules, 2005 Hexadepsipeptide 2, the precursor of Hirsutellide A (1), was synthesized in an overall yield of 45% from N-Boc-Me-Gly via three coupling reactions using dicyclohexylcarbodiimide (DCC), O-(7-azabenzotriazol-1-yl)-N,N,N’,N’-tetramethyl- uronium ...
Ligong Chen +6 more
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N-[2-(1H-Indol-3-yl)ethyl]-2-(4-isobutylphenyl)propanamide
Molbank, 2018 The compound in the title was prepared by reaction between tryptamine and ibuprofen using N,N′-dicyclohexylcarbodiimide as a “dehydrating„ reagent.
Stanimir Manolov +2 more
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Synthesis of ketoprofen - L- phenylalanine and Ketoprofen -y- Aminobutyric acid ethyl esters as possible prodrugs [PDF]
المجلة العراقية للصيدلة, 2006 Ethyl ester HCI of the amino acids -L- phenylalanine and 7- Aminobutyric acid were synthesized through reaction of these amino acids with thionyl chloride in absolute ethanol.
Muthanna D.Saud +2 more
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Phosphodiester Conjugation of Metronidazole and Dexamethasone as Possible Mutual Prodrug
Iraqi Journal of Pharmaceutical Sciences, 2017 As possible mutual prodrug had been synthesized that contain metronidazole and dexamethazone conjugated through phosphodiester linkage. The rationale for this type of conjugate is to get a prodrug with possible site – specific delivery of its active ...
Muthana D. Saud, Suhair M. Ghani
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Chemistry ProceedingsThis work presents a step-by-step synthesis of a new derivative of 1,3,5-oxadiazine. In the first step, by reacting N-(1-amino-2,2,2-trichloroethyl)acetamide with 2-bromobenzoyl isothiocyanate, a previously undescribed thiourea, N-((1-acetamido-2,2,2 ...
Valeriia V. Pavlova +5 more
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First total synthesis and biological evaluation of halolitoralin A [PDF]
Journal of the Serbian Chemical Society, 2007 A new potent bioactive alanine-rich cyclic hexapeptide halolitoralin A(8), which was previously isolated from the marine sediment-derived bacterial strain Halobacillus litoralis YS3016, has been synthesized by the solution phase technique.
RAJIV DAHIYA, DEVENDER PATHAK
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