BIOMAT Database Logo BIOMAT Database Logo

Kinetic studies of hydrogen bonding. 1-Cyclohexyluracil and 9-ethyladenine. 1968

G G Hammes, and A C Park

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D011108 Polymers Compounds formed by the joining of smaller, usually repeating, units linked by covalent bonds. These compounds often form large macromolecules (e.g., BIOPOLYMERS; PLASTICS). Polymer
D004735 Energy Transfer The transfer of energy of a given form among different scales of motion. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed). It includes the transfer of kinetic energy and the transfer of chemical energy. The transfer of chemical energy from one molecule to another depends on proximity of molecules so it is often used as in techniques to measure distance such as the use of FORSTER RESONANCE ENERGY TRANSFER. Transfer, Energy
D006859 Hydrogen The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas. Protium,Hydrogen-1
D000225 Adenine A purine base and a fundamental unit of ADENINE NUCLEOTIDES. Vitamin B 4,4, Vitamin B,B 4, Vitamin
D014498 Uracil One of four nucleotide bases in the nucleic acid RNA.

Related Publications

G G Hammes, and A C Park
Higher order associations of adenine and uracil by hydrogen bonding. I. Self-association of 9-ethyladenine and 1-cyclohexyluracil.
February 1972, Biochemistry,
G G Hammes, and A C Park
Higher order associations of adenine and uracil by hydrogen bonding. II. Formation of complexes in mixed solutions of 9-ethyladenine and 1-cyclohexyluracil.
February 1972, Biochemistry,
G G Hammes, and A C Park
Hydrogen bonding interaction of diphenylhydantoin and 9-ethyladenine.
March 1983, Molecular pharmacology,
G G Hammes, and A C Park
Characteristics of the hydrogen bonding interactions of substituted hydantoins with 9-ethyladenine.
January 1974, Molecular pharmacology,
G G Hammes, and A C Park
Cyanurate mimics of hydrogen-bonding patterns of nucleic bases: crystal structure of a 1:1 molecular complex of 9-ethyladenine and N-methylcyanuric acid.
January 2001, Organic letters,
G G Hammes, and A C Park
The effect of 9-ethyladenine on the photodimerization of 1-cyclohexylthymine.
January 1975, Photochemistry and photobiology,
G G Hammes, and A C Park
Crystal structure of the intermolecular complex 9-ethyladenine: 1-methyl-5-fluorouracil.
December 1967, Journal of molecular biology,
G G Hammes, and A C Park
The crystal structure of the intermolecular complex 9-ethyladenine: 1-methyl-5-bromouracil.
November 1966, Acta crystallographica,
G G Hammes, and A C Park
Association of CNS active drugs with 9-ethyladenine.
July 1971, Biochemical pharmacology,
G G Hammes, and A C Park
Experimental and Theoretical Studies in Hydrogen-Bonding Organocatalysis.
August 2015, Molecules (Basel, Switzerland),
Copied contents to your clipboard!